﻿<?xml version="1.0" encoding="utf-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.1 20151215//EN" "JATS-journalpublishing1.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" article-type="review-article">
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Explor Foods Foodomics</journal-id>
<journal-id journal-id-type="publisher-id">EFF</journal-id>
<journal-title-group>
<journal-title>Exploration of Foods and Foodomics</journal-title>
</journal-title-group>
<issn pub-type="epub">2837-9020</issn>
<publisher>
<publisher-name>Open Exploration Publishing</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.37349/eff.2024.00027</article-id>
<article-id pub-id-type="manuscript">101027</article-id>
<article-categories>
<subj-group>
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Ellagitannins from <italic>Eucalyptus camaldulensis</italic> and their potential use in the food industry</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0009-0009-8014-4461</contrib-id>
<name>
<surname>Sánchez-Loredo</surname>
<given-names>Eliseo</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
<role content-type="https://credit.niso.org/contributor-roles/visualization/">Visualization</role>
<role content-type="https://credit.niso.org/contributor-roles/investigation/">Investigation</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2596-8301</contrib-id>
<name>
<surname>Sepúlveda</surname>
<given-names>Leonardo</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/validation/">Validation</role>
<role content-type="https://credit.niso.org/contributor-roles/resources/">Resources</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5866-2678</contrib-id>
<name>
<surname>Wong-Paz</surname>
<given-names>Jorge E.</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/validation/">Validation</role>
<role content-type="https://credit.niso.org/contributor-roles/supervision/">Supervision</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6399-5856</contrib-id>
<name>
<surname>Palomo-Ligas</surname>
<given-names>Lissethe</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/validation/">Validation</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6428-4925</contrib-id>
<name>
<surname>Rodriguez-Herrera</surname>
<given-names>Raúl</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/validation/">Validation</role>
<role content-type="https://credit.niso.org/contributor-roles/supervision/">Supervision</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5867-8672</contrib-id>
<name>
<surname>Aguilar</surname>
<given-names>Cristóbal N.</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/validation/">Validation</role>
<role content-type="https://credit.niso.org/contributor-roles/supervision/">Supervision</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6595-863X</contrib-id>
<name>
<surname>Ascacio-Valdés</surname>
<given-names>Juan A.</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
<role content-type="https://credit.niso.org/contributor-roles/resources/">Resources</role>
<role content-type="https://credit.niso.org/contributor-roles/validation/">Validation</role>
<role content-type="https://credit.niso.org/contributor-roles/visualization/">Visualization</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="cor1">
<sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="editor">
<name>
<surname>Pinela</surname>
<given-names>José</given-names>
</name>
<role>Academic Editor</role>
<aff>Polytechnic Institute of Bragança, Portugal</aff>
</contrib>
</contrib-group>
<aff id="I1">
<sup>1</sup>Food Research Department, School of Chemistry, Autonomous University of Coahuila, Saltillo, Coahuila 25280, Mexico</aff>
<aff id="I2">
<sup>2</sup>Faculty of Professional Studies Zona Huasteca, Autonomous University of San Luis Potosí, Ciudad Valles, San Luis Potosí 79060, Mexico</aff>
<author-notes>
<corresp id="cor1">
<bold>
<sup>*</sup>Correspondence:</bold> Juan A. Ascacio-Valdés, Food Research Department, School of Chemistry, Autonomous University of Coahuila, Saltillo, Coahuila 25280, Mexico. <email>alberto_ascaciovaldes@uadec.edu.mx</email></corresp>
</author-notes>
<pub-date pub-type="ppub">
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>27</day>
<month>02</month>
<year>2024</year>
</pub-date>
<volume>2</volume>
<issue>1</issue>
<fpage>83</fpage>
<lpage>100</lpage>
<history>
<date date-type="received">
<day>27</day>
<month>09</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>04</day>
<month>01</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>© The Author(s) 2024.</copyright-statement>
<license xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>This is an Open Access article licensed under a Creative Commons Attribution 4.0 International License (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.</license-p>
</license>
</permissions>
<abstract>
<p>Plants play a key role in the treatment and prevention of diseases since ancient times. <italic>Eucalyptus</italic> has been traditionally used in the treatment of conditions related to the respiratory system, such as flu, colds, sore throats, bronchitis, as well as neuralgia, and stiffness<italic>. Eucalyptus camaldulensis</italic> has several phytoconstituents such as ellagitannins endowed with bioactivity, including antioxidant and inhibitory potential on various microorganisms causing foodborne diseases. Tellimagrandin I, pedunculagin, castalagin/vescalagin are among the most representative and have activity against pathogens such as <italic>Staphylococcus aureus</italic>, <italic>Escherichia coli</italic>, <italic>Listeria monocytogenes</italic>, and <italic>Bacillus cereus</italic>. These antioxidant ellagitannins may have potential application in the food, pharmaceutical, and cosmetic industries. The main industrial uses of <italic>E. camaldulensis</italic> are related to the production of wood, paper, and charcoal, with its leaves and branches considered by-products from these industrial activities. However, these plant by-products could be used to obtain bioactive compounds for the development of new and improved consumer goods. Therefore, the aim of this work was to review the main ellagitannins of <italic>E. camaldulensis</italic> and their antioxidant and antibacterial activities in foodborne microorganisms, as well as the relevance that these compounds may have in the food industry and related sectors.</p>
</abstract>
<kwd-group>
<kwd>Antioxidants</kwd>
<kwd>ellagitannins</kwd>
<kwd><italic>Eucalyptus camaldulensis</italic></kwd>
<kwd>foodborne microorganisms</kwd>
<kwd>natural ingredients</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p id="p-1">In human traditions, herbal medicine has played a role in treating and preventing ailments and diseases, bringing wellness to human beings [<xref ref-type="bibr" rid="B1">1</xref>]. One of the most widely used plants in traditional remedies is plants of the <italic>Eucalyptus</italic> genus. <italic>Eucalyptus</italic> has traditionally been used as a remedy for conditions related to the respiratory system [<xref ref-type="bibr" rid="B2">2</xref>] as <italic>Eucalyptus camaldulensis</italic> to treat flu, common colds, and nasal infections, through decoctions. Also, <italic>Eucalyptus globulus</italic> for asthma, cold, cough, as decoction and extracts [<xref ref-type="bibr" rid="B3">3</xref>], and in Latin America, has also been used for nasal congestion, throat pain and inflammation, chest pain, airway clearance, removal of phlegm, pharyngitis and as a disinfectant and antiseptic, either as an infusion, ointment, ointment, tea, vaporization, and aromatic water [<xref ref-type="bibr" rid="B4">4</xref>]. <italic>Eucalyptus</italic> essential oils (EOs) are among the first oils marketed in the world besides, they have bioactivity that allows them to be used in traditional remedies for the treatment of gastrointestinal disorders and wound healing, as a herbicide, and against some pests, acaricide, nematicide, its use in perfumery, soap making, in addition as an antiseptic, antioxidant, against some fungi and bacteria that can be pathogenic [<xref ref-type="bibr" rid="B5">5</xref>].</p>
<p id="p-2">Several species of the <italic>Eucalyptus</italic> genus have spread in many parts of the world due to its great qualities such as rapid growth rate and high biomass production, the ability to grow in various environments and soils, its short cellulose fiber, and the high quality of the wood, as well as its pulp for the paper industry, the timber industry for the production of plywood and solid wood [<xref ref-type="bibr" rid="B6">6</xref>] and production of EO in the cosmetic industry, since the oil of other eucalyptus species has been used in the cosmetic industry, some of the most used species were <italic>E. globulus</italic> [<xref ref-type="bibr" rid="B7">7</xref>–<xref ref-type="bibr" rid="B9">9</xref>] and <italic>Eucalyptus citriodora</italic> [<xref ref-type="bibr" rid="B5">5</xref>, <xref ref-type="bibr" rid="B10">10</xref>]. <italic>E. camaldulensis</italic> is a plant source very rich in EO with bioactive properties, and phenolic compounds, that could be used in medicine and food preservation. Thus, in the Asian continent, <italic>E. camaldulensis</italic> is used in traditional medicine to mitigate various symptoms of respiratory diseases, such as cough, sore throat, and sinusitis [<xref ref-type="bibr" rid="B3">3</xref>, <xref ref-type="bibr" rid="B11">11</xref>]. The EO of <italic>E. camaldulensis</italic> has shown a potential to inhibit malatogensis in the skin with mice and decrease intracellular oxygen reactant species, which makes its use as a skin care pharmaceutical product possible [<xref ref-type="bibr" rid="B12">12</xref>].</p>
<p id="p-3">These EO are usually recovered from various parts of the plant, ranging from wood, leaves, roots, flowers, and fruits [<xref ref-type="bibr" rid="B13">13</xref>]. Different class of secondary metabolites can be found, among which terpene compounds stand out, especially monoterpenes, sesquiterpenes, alcohols, ketones, esters, aldehydes, and phenols [<xref ref-type="bibr" rid="B5">5</xref>].</p>
<p id="p-4">Within the <italic>Eucalyptus</italic> genus, the most cultivated species in plantations are <italic>Eucalyptus grandis</italic>, <italic>E. globulus</italic>, <italic>E. camaldulensis</italic>, as well as the hybrids made from these species [<xref ref-type="bibr" rid="B6">6</xref>]. In addition, <italic>E. camaldulensis</italic> is a plant rich not only in EOs with bioactive properties, but also in the content of phenolic compounds as flavonoids and ellagitannins that can be used in medicine and food preservation [<xref ref-type="bibr" rid="B11">11</xref>]. The use of new sources of antioxidants and antimicrobials is necessary due to the potential use of these compounds and their multiple applications, avoiding the depletion of sources and taking advantage of by-products from agri-food industries. The aim of this work was to make a particular compilation about of the main ellagitannins of <italic>E. camaldulensis</italic>, and their antioxidant, antibacterial activities in food pathogenic microorganisms and the relevance that these may represent in food trends.</p>
</sec>
<sec id="s2">
<title>General information</title>
<p id="p-5">
<italic>E. camaldulensis</italic> is a plant native to Australia [<xref ref-type="bibr" rid="B11">11</xref>], known in the world as red gum, red gum Murray, red, and river gum [<xref ref-type="bibr" rid="B14">14</xref>]. It is employed industrially mainly in the paper industry (70–80%) [<xref ref-type="bibr" rid="B7">7</xref>], followed to that carbon (10–15%) and finally only 5% of the tree is used for pool construction; this type of industrial exploitation generates waste as leaves and branches that could whereas be a good potential source of bioactive compounds [<xref ref-type="bibr" rid="B11">11</xref>]. The botanic structure <italic>E. camaldulensis</italic> is composed of a bark that varies from white shades and smooth surface, dull green leaves in adulthood, narrow and pointed, the juvenile leaves are usually more oval. It has a strongly beaked operculum between 0.3–0.7 cm long at maturity and a long operculum of 0.9–1.6 cm long with curvature in some subspecies. In addition, it has a capsule that houses the seeds in its interior [<xref ref-type="bibr" rid="B14">14</xref>] (<xref ref-type="fig" rid="fig1">Figure 1</xref>). <italic>E. camaldulensis</italic> trees can generate tall forests and adapt to diverse climatic regions, from areas of high rainfall to semi-arid regions in high and low regions at sea level [<xref ref-type="bibr" rid="B6">6</xref>].</p>
<fig id="fig1" position="float">
<label>Figure 1</label>
<caption>
<p>Upper parts from <italic>E. camaldulensis</italic>. A. Leaves; B. operculum; C. capsule from <italic>E. camaldulensis</italic></p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="eff-02-101027-g001.tif" />
</fig>
</sec>
<sec id="s3">
<title>Chemical composition</title>
<p id="p-6">
<italic>E. camaldulensis</italic> is a plant with a wide variety of chemical constituents among which stand out the terpenoids, alkaloids, flavonoids, tannins, saponins, and glucosides among others such as phenolic acids as seen in <xref ref-type="table" rid="t1">Table 1</xref> [<xref ref-type="bibr" rid="B15">15</xref>], and the main compounds found is 1,8-cineole mainly in fresh leaves [<xref ref-type="bibr" rid="B16">16</xref>].</p>
<table-wrap id="t1">
<label>Table 1</label>
<caption>
<p>Volatile and phenolic profile of <italic>E. camaldulensis</italic> extracts (expressed as % in the sample) [<xref ref-type="bibr" rid="B15">15</xref>, <xref ref-type="bibr" rid="B17">17</xref>]</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th>
<bold>Class</bold>
</th>
<th>
<bold>Compound</bold>
</th>
<th>
<bold>EO (leaves, %)</bold>
</th>
<th>
<bold>Extract (leaves, %)</bold>
</th>
</tr>
</thead>
<tbody>
<tr>
<td>Monocyclic monoterpene</td>
<td>α-Pinene</td>
<td>14.68</td>
<td>-</td>
</tr>
<tr>
<td>Bicyclic monoterpene</td>
<td>Camphene</td>
<td>0.87</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>β-Pinene</td>
<td>6.66</td>
<td>-</td>
</tr>
<tr>
<td>Non-cyclic monoterpene</td>
<td>α-Pinene epoxide</td>
<td>0.27</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>γ-Terpinene</td>
<td>9.42</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>δ-Terpinene</td>
<td>1.11</td>
<td>-</td>
</tr>
<tr>
<td>Acyclic terpene</td>
<td>Isoamyl isovalerate</td>
<td>1.07</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>Fenchyl alcohol</td>
<td>0.79</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>α-Camphodenic aldehyde</td>
<td>0.66</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>Trans-pinocarveol</td>
<td>8.36</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>Mytenal</td>
<td>0.94</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>
<italic>Z</italic>-Carveol</td>
<td>1.15</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>
<italic>d</italic>-Carvone</td>
<td>0.51</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>
<italic>o</italic>-Cymen-5-ol</td>
<td>0.46</td>
<td>-</td>
</tr>
<tr>
<td>Acyclic terpene</td>
<td>Benzyl valerate</td>
<td>0.14</td>
<td>-</td>
</tr>
<tr>
<td>Bicyclic monoterpene</td>
<td>α-Gurjunene</td>
<td>0.26</td>
<td>-</td>
</tr>
<tr>
<td>Bicyclic monoterpene</td>
<td>β-Gurjunene</td>
<td>0.22</td>
<td>-</td>
</tr>
<tr>
<td>Tricyclic monoterpene</td>
<td>Aromadendrene</td>
<td>2.63</td>
<td>-</td>
</tr>
<tr>
<td>Tricyclic monoterpene</td>
<td>Alloaromadendrene</td>
<td>0.89</td>
<td>-</td>
</tr>
<tr>
<td>Tricyclic monoterpene</td>
<td>Phenethyl isovalerate</td>
<td>0.90</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>Ledene</td>
<td>0.45</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>Epiglobulol</td>
<td>1.83</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>Ledol</td>
<td>7.42</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>Viridlorol</td>
<td>1.13</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>Eremophilene</td>
<td>1.13</td>
<td>-</td>
</tr>
<tr>
<td>Monocyclic monoterpene</td>
<td>γ-Cadinene</td>
<td>0.29</td>
<td>-</td>
</tr>
<tr>
<td>Sesquiterpenes</td>
<td>Camaldulin</td>
<td>P</td>
<td>-</td>
</tr>
<tr>
<td>Sesquiterpenes</td>
<td>Ursolic acid lactone</td>
<td>P</td>
<td>-</td>
</tr>
<tr>
<td>Sesquiterpenes</td>
<td>Betulinic acid</td>
<td>P</td>
<td>-</td>
</tr>
<tr>
<td>Sesquiterpenes</td>
<td>Oleanolic acid and ursolic acid</td>
<td>P</td>
<td>-</td>
</tr>
<tr>
<td>Cyclic monoterpene</td>
<td>Eucalyptol (1–8 cineol)</td>
<td>34.42</td>
<td>-</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>HHDP-glucopyranose</td>
<td>-</td>
<td>8.07</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Galloylglucopyranose</td>
<td>-</td>
<td>4.11</td>
</tr>
<tr>
<td>Hydrolyzable tannin </td>
<td>Galloyl quinic acid</td>
<td>-</td>
<td>3.59</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Galloyl shikimic acid</td>
<td>-</td>
<td>2.44</td>
</tr>
<tr>
<td>Phenolic acid</td>
<td>Phloroglucinol derivative</td>
<td>-</td>
<td>3.41</td>
</tr>
<tr>
<td>Phenolic acid</td>
<td>Chlorogenic acid</td>
<td>-</td>
<td>14.20</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Digalloylglucopyranose</td>
<td>-</td>
<td>4.25</td>
</tr>
<tr>
<td>Flavonoid</td>
<td>Cypellocarpin B</td>
<td>-</td>
<td>8.08</td>
</tr>
<tr>
<td>Condensed tannin</td>
<td>Benzyl-galloylglucose</td>
<td>-</td>
<td>8.16</td>
</tr>
<tr>
<td>Flavonoid</td>
<td>Quercetin glucuronide</td>
<td>-</td>
<td>5.15</td>
</tr>
<tr>
<td>Flavonoid</td>
<td>Kaempferol glucuronide</td>
<td>-</td>
<td>3.36</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Galloyl-HHDP-glucopyranose</td>
<td>-</td>
<td>13.38</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Vescalagin</td>
<td>-</td>
<td>6.10</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Galloyl-HHDP-glucopyranose</td>
<td>-</td>
<td>15.09</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Pedunculagin isomer</td>
<td>-</td>
<td>9.40</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Castalagin</td>
<td>-</td>
<td>1.10</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Digalloylglucopyranose</td>
<td>-</td>
<td>2.28</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Valoneoyl-HHDP-glucopyranose</td>
<td>-</td>
<td>1.40</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Digalloylglucopyranose</td>
<td>-</td>
<td>2.28</td>
</tr>
<tr>
<td>Condensed tannin</td>
<td>pterocarinin A</td>
<td>-</td>
<td>0.56</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Valoneic acid dilactone</td>
<td>-</td>
<td>1.65</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Galloyl cypellocarpin B</td>
<td>-</td>
<td>2.59</td>
</tr>
<tr>
<td>Flavonoid</td>
<td>Quercetin pentoside</td>
<td>-</td>
<td>2.64</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Ellagic acid derivative</td>
<td>-</td>
<td>2.08</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Pedunculagin isomer</td>
<td>-</td>
<td>6.18</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Ellagitannin dimer</td>
<td>-</td>
<td>6.75</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Sanguiin H10-like ellagitannin dimer</td>
<td>-</td>
<td>9.79</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Tellimagradin I</td>
<td>-</td>
<td>31.97</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Galloyl-bis-HHDP-glucopyranose isomer</td>
<td>-</td>
<td>1.02</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Valoneoyl-digalloyl-glucopyranose</td>
<td>-</td>
<td>1.45</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Valoneic acid dilactone</td>
<td>-</td>
<td>2.70</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Tetragalloylglucopyranose</td>
<td>-</td>
<td>1.79</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Sanguiin H10-like ellagitannin dimer</td>
<td>-</td>
<td>0.47</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Ellagitannin dimers</td>
<td>-</td>
<td>18.22</td>
</tr>
<tr>
<td>Hydrolyzable tannin</td>
<td>Trigalloyl-HHDP-glucopyranose</td>
<td>-</td>
<td>2.69</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>P: for only the compounds present without identifying the percentage; HHDP: hexahydroxy diphenic acid; -: not involving</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p id="p-7">Moreover, other chemical constituents very important and high value reported for <italic>E. camaldulensis</italic> are phenolic compounds among which are flavonoids, and ellagitannins in more abundance. The total content of polyphenols in this species was estimated to be about 364.1 mg ± 8.2 mg, data reported in gallic acid equivalents, of which about 80.5 mg ± 0.9 mg appear to be flavonoids determined as quercetin equivalents [<xref ref-type="bibr" rid="B17">17</xref>].</p>
<p id="p-8">Extraction is the most important step to obtain phenolic compounds from plant sources and this can be carried out by various extractions and solvents [<xref ref-type="bibr" rid="B18">18</xref>]. It has been possible to extract compounds from <italic>E. camaldulensis</italic> with different solvents. The use of different solvents varies in the type of compounds extracted as well as the amount, which makes the difference in obtaining these [<xref ref-type="bibr" rid="B17">17</xref>]. For example, flavonoids can be found in ether-soluble fractions of leaf extracts [<xref ref-type="bibr" rid="B10">10</xref>]. Whereas among the compounds found in aqueous fractions are flavones, different glycosides, and important phenolic compounds like phenolic acids, ellagitannins and their derivates, gallotannins and phloroglucinol derivatives [<xref ref-type="bibr" rid="B17">17</xref>]. It may also present other compounds such as alkaloids, caffeine derivatives, purine derivatives, and some acids [<xref ref-type="bibr" rid="B19">19</xref>].</p>
<p id="p-9">Also, the extract in acetone was reported as rich in bioactive compounds as the ellagitannins pedunculagin and tellimagrandin I, flavonols, as well as terpenoids. Other fractions with 60% methanol have allowed the separating of ellagitannins, ellagitannins isomer, and ellagitannin dimers mainly among they are pedunculagin isomer and other compounds [<xref ref-type="bibr" rid="B17">17</xref>] as can be seen in <xref ref-type="table" rid="t1">Table 1</xref>.</p>
<p id="p-10">Although <italic>E. camaldulensis</italic> has compounds that could be beneficial, it also has saponins, which could have a negative effect on health. On the other hand, it has also been reported that <italic>E. camaldulensis</italic> can retain trace elements such as zinc (Zn), copper (Cu), arsenic (As), magnesium (Mg), calcium (Ca), sulfur (S), iron (Fe), aluminum (Al), boron (B) [<xref ref-type="bibr" rid="B11">11</xref>, <xref ref-type="bibr" rid="B19">19</xref>]. However, through conventional extractions for traditional treatments it has not been reported that dangerous quantities are extracted [<xref ref-type="bibr" rid="B20">20</xref>].</p>
</sec>
<sec id="s4">
<title>Ellagitannins in <italic>E. camaldulensis</italic></title>
<p id="p-11">In <italic>E. camaldulensis</italic> there are three main classes of bioactive compounds among are ellagitannins, flavonoids, and terpenes [<xref ref-type="bibr" rid="B17">17</xref>]. Flavonoids have been reported as one of the main compounds in <italic>E. camaldulensis</italic> [<xref ref-type="bibr" rid="B21">21</xref>], possessing antiviral, antioxidant, antibacterial and anticancer properties, as well as providing flavor to flowers, fruits, and seeds in plants [<xref ref-type="bibr" rid="B22">22</xref>]. Also, <italic>E. camaldulensis</italic> have terpenes and terpenoids [<xref ref-type="bibr" rid="B23">23</xref>] commonly present in EOs, which possess antimicrobial, antioxidant, anti-allergic and anticancer activities [<xref ref-type="bibr" rid="B24">24</xref>]. Apart from that, ellagitannins have only been found in parts such as leaves [<xref ref-type="bibr" rid="B17">17</xref>, <xref ref-type="bibr" rid="B25">25</xref>, <xref ref-type="bibr" rid="B26">26</xref>] in bark and wood [<xref ref-type="bibr" rid="B27">27</xref>, <xref ref-type="bibr" rid="B28">28</xref>] as well as in seeds [<xref ref-type="bibr" rid="B29">29</xref>] but there have not been many recent reports where ellagitannins are present in <italic>E. camaldulensis</italic>. EOs have been recovered from bark, buds, flowers, fruits, leaves, husks, or roots, however, the yield of these is low and the use of solvents such as petroleum ether, ether, and hexane among others is necessary [<xref ref-type="bibr" rid="B24">24</xref>], unlike oils, ellagitannins can be recovered with ethanol, methanol, and aqueous mixtures. In addition, the bioactivity of ellagitannins has shown great variety due to their structure. Ellagitannins are an important group of phytochemicals, these compounds belong to the hydrolyzable tannins that have a high bioactivity value. Ellagitannins represent the defense in fruits and nuts, and they are phytochemicals with antioxidant powder, anticancer, and anti-atherosclerotic properties. Ellagitannins are hydrolyzable tannins with abased HHDP esterified to a polyol core. They can be found in plants as secondary metabolites, where one of their main roles is defense, and are found in flowers, leaves, stalks, peels, and fruits. They are localized in the cytoplasm and cell vacuoles [<xref ref-type="bibr" rid="B30">30</xref>, <xref ref-type="bibr" rid="B31">31</xref>], and among fruits that can contain ellagitannins are the berries, contributing to the health of the fruit itself due to the antioxidant properties of these compounds [<xref ref-type="bibr" rid="B32">32</xref>].</p>
<p id="p-12">The use of different solvents varies in the type of compounds extracted as well as the amount, which makes the difference in obtaining these [<xref ref-type="bibr" rid="B33">33</xref>]. Solvents with water allow the extraction of different compounds like ellagitannins [<xref ref-type="bibr" rid="B34">34</xref>]. Been reported some ellagitannins in extracts from <italic>E. camaldulensis</italic> with acetone: water, highlighting HHDP-glucopyranose, as well as galloyl-HHDP-glucopyranose positional isomers, pedunculagin, tellimagrandin I, and ellagitannins dimers. Furthermore, other compounds are found in aqueous fractions such as HHDP-glucopyranose, and galloyl-HHDP-glucopyranose [<xref ref-type="bibr" rid="B17">17</xref>].</p>
<p id="p-13">Acetone and ethanol have played an important role in the extraction of different compounds from <italic>E. camaldulensis</italic> that has allowed to recovery of these solvents. Has been reported to extract HHDP, which is an intermediary molecule in obtaining ellagic acid [<xref ref-type="bibr" rid="B35">35</xref>]. On the other hand, methanol has presented a role in the recovery of ellagitannins. Methanol allowed the recovery of ellagitannins, mainly pedunculagin isomers, ellagitannin dimer, sanguine H10 like ellagitannin dimer, tellimagrandin I, galloyl-bis-HHDP-glucopyranose isomer, and in fractions with methanol to 100% can be found dimers from ellagitannins in greater quantity as sanguiin H10-like ellagitannin dimer too, in addition to galloyl-HHDP-glucopyranose, vescalagin, galloyl-HHDP-glucopyranose, castalagin, digalloylglucopyranose, valoneoyl-HHDP-glucopyranose, pterocarinin A, valoneic acid dilactone, galloyl cypellocarpin B, quercetin pentoside, and ellagic acid derivative [<xref ref-type="bibr" rid="B17">17</xref>].</p>
<p id="p-14">These compounds possess antibacterial, antifungal, antidiabetic, and antioxidant activity, antimutagenic, and antiproliferative activities [<xref ref-type="bibr" rid="B32">32</xref>]. Among all the compounds of <italic>E. camaldulensis</italic> leaves, ellagitannins such as telimagrandin I, pedunculagin, vescalagin and castalagin stand out for their structure [<xref ref-type="bibr" rid="B17">17</xref>, <xref ref-type="bibr" rid="B27">27</xref>] (see <xref ref-type="fig" rid="fig2">Figure 2</xref>). However, there are not many reports mentioning the presence of ellagitannins in the plant.</p>
<fig id="fig2" position="float">
<label>Figure 2</label>
<caption>
<p>Chemical structures of tellimagrandin I, pedunculagin, and vescalagin/castalagin</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="eff-02-101027-g002.tif" />
</fig>
<p id="p-15">Other species of <italic>E. globulus</italic> have reported the presence of ellagitannins such as pedunculaginm tellimagrandin I and II, hexahydroxydiphenoyl-β-<italic>D</italic>-glucose, as ellagic acid in leaves [<xref ref-type="bibr" rid="B36">36</xref>, <xref ref-type="bibr" rid="B37">37</xref>] and wood [<xref ref-type="bibr" rid="B28">28</xref>]. nitens ellagic acid, HHDP-glucose, pedunculagin, tellimagrandin I and II, HHDP-digalloylglucose, casuarinin, casuarictin, Di-HHDP-galloylglucose, HHDP-trigalloylglucose in wood [<xref ref-type="bibr" rid="B38">38</xref>] as well as in <italic>E. citriodora</italic>, pedunculagin, vescalagin/castalagin, acustissimin A, pterocarinin A, tellimagrandin I, and casuarininin have also been found [<xref ref-type="bibr" rid="B39">39</xref>], however, there are reports in the literature on other <italic>Eucalyptus</italic> species.</p>
</sec>
<sec id="s5">
<title>
<italic>E. camaldulensis</italic> and foodborne pathogens</title>
<p id="p-16">Foodborne pathogens are disease-causing pathogens that come from contaminated food somewhere in the food chain [<xref ref-type="bibr" rid="B40">40</xref>]. These microorganisms are the cause of various diseases that not only affect health but also the economy of the people [<xref ref-type="bibr" rid="B41">41</xref>]. Foodborne pathogens have caused a cost in the treatment of foodborne illnesses of around $55.5 billion annually in the United States and are dangerous because of the population that is more susceptible to them, such as the elderly, immunocompromised people, infants, and pregnant women [<xref ref-type="bibr" rid="B42">42</xref>]. However, even with technology applied to food safety, the foodborne illness still represents a public health problem [<xref ref-type="bibr" rid="B43">43</xref>].</p>
<p id="p-17">Among the most common microorganisms that cause foodborne illness are: <italic>Staphylococcus aureus</italic>, <italic>Shigella</italic> spp., <italic>Salmonella</italic> spp., <italic>Yersinia enterocolitica</italic>, <italic>Escherichia coli</italic>, <italic>Listeria monocytogenes</italic>, <italic>Vibrio</italic> spp<italic>.</italic>, <italic>Cronobacter sakazakii</italic>, <italic>Bacillus cereus</italic>, <italic>Campylobacter jejuni</italic>, <italic>Clostridium botulinum</italic>, <italic>Clostridium perfringens</italic>, not to mention viruses and parasites such as viruses as hepatitis A and noroviruses as well as the parasites <italic>Toxoplasma gondii</italic>, <italic>Cyclospora cayetanensis</italic>, and <italic>Trichinella spiralis</italic> [<xref ref-type="bibr" rid="B41">41</xref>]. Besides, some of these microorganisms cause the deterioration of food in physical appearance, aroma, nutritional value and not only diseases [<xref ref-type="bibr" rid="B42">42</xref>].</p>
<p id="p-18">Pathogenic microorganisms are a problem of great relevance and seriousness for health today, due to the resistance that these microorganisms have developed [<xref ref-type="bibr" rid="B44">44</xref>]. These microorganisms contaminate numerous food products, such as fruits, vegetables, water, seafood, cereals, and meat, dairy products, and during food processing the equipment and the human operator can be used to process food [<xref ref-type="bibr" rid="B42">42</xref>].</p>
<p id="p-19">The use of antimicrobial agents prevents the proliferation of microorganisms that cause food spoilage [<xref ref-type="bibr" rid="B11">11</xref>]. Some of secondary metabolites produced by various natural sources such as plants have antimicrobial potential against pathogenic microorganisms and can inhibit virulence factors [<xref ref-type="bibr" rid="B1">1</xref>]. These compounds with antibacterial properties have been used in food processing, acting as preservatives and preventing the deterioration of food products both in food pathogenic and non-pathogenic microorganisms [<xref ref-type="bibr" rid="B19">19</xref>], and have also been used antioxidant, and antitumor activities [<xref ref-type="bibr" rid="B44">44</xref>].</p>
<p id="p-20">It has been reported that medicinal plant extracts such as <italic>Eucalyptus</italic> have shown activity against microorganisms, including <italic>B. cereus</italic>, <italic>Alicyclobacillus acidoterrestris</italic>, <italic>Enterococcus faecalis</italic>, and <italic>E. coli</italic>, <italic>Propionibacterium acnes</italic>, <italic>S. aureus</italic>, and methicillin-resistant <italic>S. aureus</italic> (MRSA), <italic>Trichophyton mentagrophytes</italic> [<xref ref-type="bibr" rid="B5">5</xref>].</p>
<p id="p-21">Crude extracts of <italic>E. camaldulensis</italic> leaves have been reported to contain phenolic compounds with antimicrobial properties effective against <italic>L. monocytogenes</italic>, <italic>S. aureus</italic>, and <italic>B. cereus</italic> [<xref ref-type="bibr" rid="B11">11</xref>]. In addition, minimum inhibitory concentrations (MIC) of ethanol fraction have been reported between 16–64 µg/mL. As well as MIC of 158–316 µg/mL and minimum bactericidal concentrations (MBC) of 316–2,528 µg/mL of aqueous fraction of <italic>E. camaldulensis</italic> [<xref ref-type="bibr" rid="B11">11</xref>]. Also, <italic>Eucalyptus</italic> EOs have been tested on <italic>E. coli</italic> and <italic>S. aureus</italic>. Other reports have shown that EOs of <italic>E. camaldulensis</italic> have demonstrated inhibition on other microorganisms including <italic>S. aureus</italic>, <italic>E. coli</italic>, <italic>Salmonella enteritidis</italic>, <italic>Bacillus subtilis</italic>, and <italic>Enterococcus faecalis</italic> [<xref ref-type="bibr" rid="B16">16</xref>] (see <xref ref-type="table" rid="t2">Table 2</xref>).</p>
<table-wrap id="t2">
<label>Table 2</label>
<caption>
<p>
<italic>E. camaldulensis</italic> inhibition of bacterial growth</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th>
<bold>Microorganism</bold>
</th>
<th>
<bold>MIC concentration</bold>
</th>
<th>
<bold>Type of extract</bold>
</th>
<th>
<bold>Part of the plant</bold>
</th>
<th>
<bold>Reference</bold>
</th>
</tr>
</thead>
<tbody>
<tr>
<td rowspan="3">
<italic>B. cereus</italic>
</td>
<td>16 µg/mL</td>
<td>Ethanol</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B11">11</xref>]</td>
</tr>
<tr>
<td>158 µg/mL</td>
<td>Aqueous</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B11">11</xref>]</td>
</tr>
<tr>
<td>31.36 µg/mL</td>
<td>EO</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B16">16</xref>]</td>
</tr>
<tr>
<td rowspan="2">
<italic>L.monocytogenes</italic>
</td>
<td>32–64 µg/mL</td>
<td>Ethanol</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B11">11</xref>]</td>
</tr>
<tr>
<td>316 µg/mL</td>
<td>Aqueous</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B11">11</xref>]</td>
</tr>
<tr>
<td rowspan="4">
<italic>S. aureus</italic>
</td>
<td>32 µg/mL</td>
<td>Ethanol</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B11">11</xref>]</td>
</tr>
<tr>
<td>158 µg/mL</td>
<td>Aqueous</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B11">11</xref>]</td>
</tr>
<tr>
<td>100 µl/mL</td>
<td>EO</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B45">45</xref>]</td>
</tr>
<tr>
<td>33.2 µg/mL</td>
<td>EO</td>
<td>leaves</td>
<td>[<xref ref-type="bibr" rid="B16">16</xref>]</td>
</tr>
<tr>
<td rowspan="2">
<italic>E. coli</italic>
</td>
<td>100 µl/mL</td>
<td>EO</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B45">45</xref>]</td>
</tr>
<tr>
<td>85 µg/mL</td>
<td>EO</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B16">16</xref>]</td>
</tr>
<tr>
<td>
<italic>Salmonella enteritis</italic>
</td>
<td>51.36 µg/mL</td>
<td>EO</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B16">16</xref>]</td>
</tr>
<tr>
<td>
<italic>Enterococcus faecalis</italic>
</td>
<td>30.0 µg/mL</td>
<td>EO</td>
<td>Leaves</td>
<td>[<xref ref-type="bibr" rid="B16">16</xref>]</td>
</tr>
</tbody>
</table>
</table-wrap>
<p id="p-22">On the other hand, <italic>Eucalyptus</italic> oil has shown antimicrobial activity, which has been mainly attributed to several compounds, among which terpenes such as 1,8-cineole, α-pinene, β-pinene, and limonene stand out [<xref ref-type="bibr" rid="B5">5</xref>]. <italic>E. camaldulensis</italic> oil has shown bioactivity on gram-positive bacteria that are more sensitive compared to gram-negative bacteria. This activity increased with increasing EO; however, at lower concentrations of 0.5 g/kg no activity was observed, and for gram-positive bacteria (<italic>S. aureus</italic> and <italic>Streptococcus</italic>). <italic>E. camaldulensis</italic> leaf EO showed activity at 1.0 g/kg and 5.0 g/kg, while for gram-negative bacteria such as <italic>S. enteritidis</italic>, <italic>Klebsiella pneumonia</italic>, <italic>Pseudomonas aeruginosa</italic>, and <italic>E. coli</italic> it was 1 g/kg and 15 g/kg, respectively. In addition, the MBC against <italic>S. aureus</italic>, <italic>Streptococcus aureus</italic>, and <italic>E. coli</italic> was shown to be 5 g/kg, 10 g/kg, and 25 g/kg, respectively [<xref ref-type="bibr" rid="B5">5</xref>] as can be seen in <xref ref-type="table" rid="t2">Table 2</xref>.</p>
</sec>
<sec id="s6">
<title>Ellagitannins from <italic>E. camaldulensis</italic> and their potential in foodstuffs</title>
<sec id="t6-1">
<title>Tellimagrandin I</title>
<p id="p-23">One of the ellagitannin found in <italic>E. camaldulensis</italic> is tellimagrandin I that abound mainly in the young leaves in April and these after are replaced for casuarinin in July, that later change to pedunculagin. These compounds are the principal tannins that are found in the leaves from summer to fall [<xref ref-type="bibr" rid="B46">46</xref>]. Tellimagrandin is made up of a molecule of HHDP and a <italic>D</italic>-glucopyranosyl with two galloyl units and this molecule has been widely used against bacterial and viral infections [<xref ref-type="bibr" rid="B47">47</xref>].</p>
</sec>
<sec id="t6-2">
<title>Effect of tellimagrandin I on pathogenic bacteria</title>
<p id="p-24">Tellimagrandin I has been effective in the inhibition of <italic>S. aureus</italic> and <italic>E. coli</italic> [<xref ref-type="bibr" rid="B48">48</xref>, <xref ref-type="bibr" rid="B49">49</xref>]. It has been reported that tellimagrandin I isolated from the rose extract was effective in reducing the MIC of oxacillin against methicillin-resistant <italic>S. aureus</italic>, acting together with tellimagrandin I and oxacillin. Reducing the MIC of oxacillin from 128 µg/mL to 1 µg/mL, when 50 µg/mL of tellimagrandin I was added to the medium [<xref ref-type="bibr" rid="B50">50</xref>]. On the other hand, tellimagrandin I also contributed to the reduction of the MIC of tetracycline in the MRSA strains <italic>OM481</italic>, <italic>OM505</italic>, <italic>OM504</italic>, and <italic>OM506</italic>. In addition, the MIC of other antibiotics such as benzylpenicillin and ampicillin was reduced with the addition of tellimagrandin I to MRSA [<xref ref-type="bibr" rid="B50">50</xref>].</p>
<p id="p-25">
<italic>S. aureus</italic> is one of the ten main microorganisms causing a food illness produced by bacteria and safety indicators. The foods most susceptible to contamination by <italic>S. aureus</italic> are all those that have had contact with animal skin, among which dairy meat and sausage products stand out [<xref ref-type="bibr" rid="B51">51</xref>, <xref ref-type="bibr" rid="B52">52</xref>].</p>
<p id="p-26">Also, the effect of isolated tellimagrandin I monomers was favorable against 32 strains of <italic>Helicobacter pylori</italic>. However, on <italic>E. coli</italic> only a MIC greater than 100 µg/mL could be obtained. In addition, the bactericidal effect of tellimagrandin I could be demonstrated according to time and dose against <italic>H. pylori in vitro</italic> showing that the effect is faster with 50 µg/mL [<xref ref-type="bibr" rid="B53">53</xref>]. Several extracts rich in tellimagrandin I extracts, and the pure compound isolated from <italic>E. globulus</italic>, has to be effective on bacteria such as <italic>S. aureus</italic> [<xref ref-type="bibr" rid="B54">54</xref>]. Its antimicrobial potential has also been proven by Boulekbache-Makhlouf et al. [<xref ref-type="bibr" rid="B55">55</xref>], who reported that extracts of <italic>E. globulus</italic> rich in tellimagrandin I inhibit <italic>S. aureus</italic> and <italic>B. subtilis</italic>.</p>
<p id="p-27">It has been reported that tellimagrandin I on MRSA acts on penicillin-binding protein 2a (PBP2a) decreasing its production and inactivating it [<xref ref-type="bibr" rid="B56">56</xref>]. PBP is a protein enables resistance to β-lactam antibiotic drugs in MRSA, PBP2a is encoded by the <italic>mecA</italic> gene found in MRSA strains, which gives resistance to beta-lactam antibiotics due to its low affinity for them, and PBP2a provides transpeptidase activity to allow cell wall synthesis at concentrations that inhibit the sensitive PBPs normally produced by <italic>S. aureus</italic> [<xref ref-type="bibr" rid="B57">57</xref>]. Likewise, in E. coli, the characteristics of the free galloyl groups of the ellagitannins increase the hydrophobicity of the structure, promoting their interaction with bacterial lipid membranes [<xref ref-type="bibr" rid="B58">58</xref>], through inactivation of essential surface proteins, interaction with membrane lipids and causing membrane phase separation [<xref ref-type="bibr" rid="B59">59</xref>].</p>
</sec>
<sec id="t6-3">
<title>Pedunculagin</title>
<p id="p-28">Among the important ellagitannins found in leaves of <italic>E. camaldulensis</italic> is pedunculagin [<xref ref-type="bibr" rid="B60">60</xref>]. Pedunculagin is a phenolic compound belonging to group of the ellagitannins which exhibit various antioxidant, anti-inflammatory, antitumor, gastroprotective, and hepaprotective activities [<xref ref-type="bibr" rid="B61">61</xref>].</p>
</sec>
<sec id="t6-4">
<title>Effect of pedunculagin on pathogenic bacteria</title>
<p id="p-29">In phenolic compounds, antibacterial activity is one of the most sought-after due to its great capacity to inhibit pathogenic bacteria and the bactericidal effect that some of them have [<xref ref-type="bibr" rid="B62">62</xref>]. In antibacterial activity, pedunculagin has shown an anti-hemolytic effect on <italic>S. aureus</italic> [<xref ref-type="bibr" rid="B63">63</xref>] as well as in fractions of pedunculagin-rich extracts [<xref ref-type="bibr" rid="B64">64</xref>, <xref ref-type="bibr" rid="B65">65</xref>], which is a bacterium commonly found in some foods causing food poisoning, being the main cause of food poisoning worldwide [<xref ref-type="bibr" rid="B51">51</xref>]. Anti-hemolytic effect is important due to the hemolysis produced by the alpha toxin of <italic>S. aureus</italic>. This hemolytic toxin causes the rupture of the red blood cell membrane. The α-hemolysin binds to the cell surface and facilitates the transport of molecules such as potassium ion (K<sup>+</sup>) and Ca<sup>2+</sup> ions, which causes necrotic death of the host cell [<xref ref-type="bibr" rid="B66">66</xref>], On the other hand, fractions obtained from <italic>Clidemia hirta,</italic> rich in pedunculagin have been effective to inhibit <italic>E. coli</italic> at concentrations greater than 100 μg/mL [<xref ref-type="bibr" rid="B64">64</xref>], as well as extracts of <italic>Geum rivale</italic> L. rich in pedunculagin were able to inhibit <italic>E. coli</italic> and <italic>L. monocytogenes</italic> at lower concentrations [<xref ref-type="bibr" rid="B65">65</xref>].</p>
<p id="p-30">The individual activity of ellagitannins has not been extensively studied, but some of the mechanisms on which they act are the ability to interact with the cell wall and nucleic acids [<xref ref-type="bibr" rid="B67">67</xref>], however it has been proven that pedunculagin decreases the ability of <italic>S. aureus</italic> to cause hemolysis, as well as some phenolic groups cause enzymatic inactivity due to their hydroxyl groups, as well as affect the cell membrane by forming complexes with proteins and polysaccharides [<xref ref-type="bibr" rid="B63">63</xref>].</p>
</sec>
<sec id="t6-5">
<title>Effect of vescalagin and castalagin on pathogenic bacteria</title>
<p id="p-31">It has been proven that ellagitannins such as vescalagin/castalagin isolate have bactericidal capacity on one of the main food pathogenic bacteria which is <italic>S. aureus</italic> [<xref ref-type="bibr" rid="B44">44</xref>].</p>
<p id="p-32">In addition, extracts rich in vescalagin and castalagin have also shown antibacterial activity on several foodborne pathogens [<xref ref-type="bibr" rid="B68">68</xref>]. Extracts of <italic>Myrciaria cauliflora</italic> seeds with high values of vescalagin and castalagin (1,999 mg/100 g ± 24 mg/100 g and 1,872 mg/100 g ± 18 mg/100 g respectively) have shown inhibition against microorganisms such as <italic>L. monocytogenes</italic>, <italic>Salmonella typhimurium</italic>, <italic>S. Enteritidis</italic>, <italic>B. cereus</italic>, <italic>E. coli</italic>, <italic>S. aureus</italic> [<xref ref-type="bibr" rid="B69">69</xref>]. <italic>Myrciaria dubia</italic> extract has also reported activity against <italic>S. typhimurium</italic>, <italic>E. coli, B. cereus</italic>, <italic>S. aureus</italic>, and <italic>L. monocytogenes</italic> [<xref ref-type="bibr" rid="B70">70</xref>].</p>
<p id="p-33">Fujita et al. [<xref ref-type="bibr" rid="B71">71</xref>] have also reported inhibition of <italic>Myrciaria dubia</italic> McVaugh rich in vescalagin and castalagin too, possess antibacterial activity on <italic>S. aureus</italic> at concentrations ranging 0.08–0.63 mg/ml. It has been demonstrated that vescalagin and castalagin have been able to inhibit microorganisms with extracts rich in these ellagitannins, as in the case of <italic>Lythrum salicaria</italic> L. acting on <italic>E. coli</italic>, <italic>B. cereus</italic>, <italic>B. subtilis</italic>, <italic>Staphylococcus epidermidis</italic>, <italic>S. aureus</italic>, <italic>S. enteritidis</italic>, <italic>S. typhimurium</italic> [<xref ref-type="bibr" rid="B72">72</xref>]. In addition, other microorganisms have been inhibited by vescalagin and castalagin, such as methicillin-resistant <italic>S. epidermidis</italic>, methicillin-resistant <italic>S. aureus</italic>, <italic>Pseudomonas aeruginosa</italic>, breaking and inhibiting the films by modulating the assembly of peptidoglycans on the bacterial surface, breaking the cell wall and bacterial death [<xref ref-type="bibr" rid="B44">44</xref>]. The inhibition concentrations of tellimagrandin I, pedunculagin, castalagin and vescalagin on food pathogenic bacteria are shown in <xref ref-type="table" rid="t3">Table 3</xref>.</p>
<table-wrap id="t3">
<label>Table 3</label>
<caption>
<p>Antibacterial activity of tellimagrandin I, pedunculagin, and vescalagin/castalagin</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th>
<bold>Microorganism</bold>
</th>
<th>
<bold>Ellagitannins</bold>
</th>
<th>
<bold>Inhibition of microorganisms at MIC</bold>
</th>
<th>
<bold>Reference</bold>
</th>
</tr>
</thead>
<tbody>
<tr>
<td rowspan="7">
<italic>E. coli</italic>
</td>
<td rowspan="2">Tellimagrandin I</td>
<td>50 µg/mL</td>
<td>[<xref ref-type="bibr" rid="B53">53</xref>]</td>
</tr>
<tr>
<td>500 ppm</td>
<td>[<xref ref-type="bibr" rid="B54">54</xref>]</td>
</tr>
<tr>
<td rowspan="2">Pedunculagin</td>
<td>&gt; 100 μg/mL</td>
<td>[<xref ref-type="bibr" rid="B64">64</xref>]</td>
</tr>
<tr>
<td>15.6 μg/mL</td>
<td>[<xref ref-type="bibr" rid="B65">65</xref>]</td>
</tr>
<tr>
<td rowspan="3">Vescalagin/Castalagin</td>
<td>9.04 mm ± 0.65 mm</td>
<td>[<xref ref-type="bibr" rid="B69">69</xref>]</td>
</tr>
<tr>
<td>6.74 mm ± 0.80 mm</td>
<td>[<xref ref-type="bibr" rid="B70">70</xref>]</td>
</tr>
<tr>
<td>2.5 mg/mL</td>
<td>[<xref ref-type="bibr" rid="B72">72</xref>]</td>
</tr>
<tr>
<td rowspan="8">
<italic>S. aureus</italic>
</td>
<td rowspan="2">Tellimagrandin I</td>
<td>50 µg/mL</td>
<td>[<xref ref-type="bibr" rid="B50">50</xref>]</td>
</tr>
<tr>
<td>1,000 ppm</td>
<td>[<xref ref-type="bibr" rid="B54">54</xref>]</td>
</tr>
<tr>
<td rowspan="2">Pedunculagin</td>
<td>&lt; 100 ug/mL</td>
<td>[<xref ref-type="bibr" rid="B64">64</xref>]</td>
</tr>
<tr>
<td>15.6 μg/mL</td>
<td>[<xref ref-type="bibr" rid="B65">65</xref>]</td>
</tr>
<tr>
<td rowspan="4">Vescalagin/Castalagin</td>
<td>9.47 mm ± 1.86 mm</td>
<td>[<xref ref-type="bibr" rid="B69">69</xref>]</td>
</tr>
<tr>
<td>9.70 mm ± 1.92 mm</td>
<td>[<xref ref-type="bibr" rid="B70">70</xref>]</td>
</tr>
<tr>
<td>0.08–0.63 mg/mL</td>
<td>[<xref ref-type="bibr" rid="B71">71</xref>]</td>
</tr>
<tr>
<td>0.625 mg/mL</td>
<td>[<xref ref-type="bibr" rid="B72">72</xref>]</td>
</tr>
<tr>
<td>
<italic>H. pylori</italic>
</td>
<td>Tellimagrandin I</td>
<td>12.5 µg/mL</td>
<td>[<xref ref-type="bibr" rid="B54">54</xref>]</td>
</tr>
<tr>
<td rowspan="3">
<italic>L. monocytogenes</italic>
</td>
<td>Pedunculagin</td>
<td>62.5 μg/mL</td>
<td>[<xref ref-type="bibr" rid="B65">65</xref>]</td>
</tr>
<tr>
<td rowspan="2">Vescalagin/Castalagin</td>
<td>8.87 mm ± 0.49 mm</td>
<td>[<xref ref-type="bibr" rid="B69">69</xref>]</td>
</tr>
<tr>
<td>8.58 mm ± 0.82 mm</td>
<td>[<xref ref-type="bibr" rid="B70">70</xref>]</td>
</tr>
<tr>
<td rowspan="3">
<italic>B. cereus</italic>
</td>
<td rowspan="3">Vescalagin/Castalagin</td>
<td>8.07 mm ± 0.96 mm</td>
<td>[<xref ref-type="bibr" rid="B69">69</xref>]</td>
</tr>
<tr>
<td>9.04 mm ± 1.36 mm</td>
<td>[<xref ref-type="bibr" rid="B70">70</xref>]</td>
</tr>
<tr>
<td>2.5 mg/mL</td>
<td>[<xref ref-type="bibr" rid="B72">72</xref>]</td>
</tr>
</tbody>
</table>
</table-wrap>
<p id="p-34">The antibacterial activity of castalagin and vescalagin have also been shown to interact with PBP2a in MRSA, rendering the bacteria susceptible to lysis and its inhibition [<xref ref-type="bibr" rid="B46">46</xref>]. In addition, extracts with castalagin act on <italic>H. pylori</italic>, preventing adhesion to the gastric mucosa, as well as allowing the disintegration of the membrane of salmonella and <italic>B. subtilis</italic> [<xref ref-type="bibr" rid="B73">73</xref>].</p>
</sec>
</sec>
<sec id="s7">
<title>Antioxidant activity</title>
<sec id="t7-1">
<title>Antioxidant effect of tellimagrandin I</title>
<p id="p-35">Tellimagrandin has been found in different extracts as <italic>Cornus mas</italic> L. These extracts have had antioxidant activity at 2,2-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), ferric reducing antioxidant power assay (FRAP), and 2,2-diphenyl-1-picrylhydrazyl (DPPH) with a range of 255.9 mmol/100 g ± 8.48 mmol/100 g, 210.62 mmol/100 g ± 5.45 mmol/100 g, 191.00 mmol/100 g ± 0.04 mmol of Trolox (Tx)/100 g respectively [<xref ref-type="bibr" rid="B74">74</xref>]. In an essay on the antioxidant capacity of some ellagitannins performed by Moilanen et al. [<xref ref-type="bibr" rid="B75">75</xref>] with tellimagrandin showed radical scavenging antioxidant properties at concentrations of 3 mmol/L and 5 mmol/L, however, at fewer concentrations they exhibited prooxidant activity enhancing the degradation of 2-deoxyribose used in the assay.</p>
<p id="p-36">Within the <italic>Eucalyptus</italic> genus, it has been mentioned that they are high in ellagitannins among they are tellimagrandin I, with high antioxidant potential, as is <italic>E. globulus</italic> with extracts, where the presence of ellagitannins is higher and gives it activity [<xref ref-type="bibr" rid="B76">76</xref>]. Furthermore, in extracts of <italic>Plinia cauliflora</italic>, showed a DPPH inhibitory concentration (IC<sub>50</sub>) of 1.45 µg/mL ± 0.02 µg/mL, as well as a peroxidation inhibition greater than 70% [<xref ref-type="bibr" rid="B77">77</xref>].</p>
</sec>
<sec id="t7-2">
<title>Antioxidant effect of pedunculagin</title>
<p id="p-37">Due to its antioxidant potential, pedunculagin has been one of the ellagitannins of great interest. Extracts from natural sources such as walnuts have been identified with the presence of pedunculagin, obtaining antioxidant potential by inhibiting lipid peroxidation in mice, as well as the ferric reducing antioxidant power [<xref ref-type="bibr" rid="B78">78</xref>]. However, the antioxidant capacity of <italic>Eucalyptus</italic> isolates has also provided antioxidant activity on DPPH and ABTS [<xref ref-type="bibr" rid="B79">79</xref>]. Other extracts, including <italic>Geum rivale</italic> L. extract with the presence of pedunculagin, have shown antioxidant potential with great inhibition against DPPH (about 90%) and ABTS [<xref ref-type="bibr" rid="B65">65</xref>].</p>
<p id="p-38">Due to the number of compounds found in crude plant extracts or residues, chromatography is usually performed to allow the recovery of fractions with more specific compounds in each one. Oliveira et al. [<xref ref-type="bibr" rid="B80">80</xref>] in 3 feijoa fractions with the presence of pedunculagin reported antioxidant potential on ABTS.</p>
<p id="p-39">In addition, pedunculagin from <italic>Quercus mongolica in vitro</italic> has been evaluated for inhibition of inflammatory cytokines [interleukin-6 (IL-6) and IL-8], as well as 5α-reductase inhibitory activity by western blotting, being pedunculagin were able to inhibit nitric oxide production, as well as decrease IL-6 and IL-8, and exhibited potent 5α-reductase type 1 inhibitory activity [<xref ref-type="bibr" rid="B81">81</xref>].</p>
</sec>
<sec id="t7-3">
<title>Antioxidant potential of vescalagin/castalagin</title>
<p id="p-40">Interestingly, in antioxidant and prooxidant assays, castalagin/vescalagin has exhibited the opposite of antioxidant for 2-deoxyribose used in the assay, obtaining prooxidant results at concentrations from 1–5 mmol/L [<xref ref-type="bibr" rid="B75">75</xref>]. Other reports on isolated vescalagin have reported around 5 mg/L for DPPH inhibition, however, from the same extract castalagin contained slightly low values compared to that of castalagin [<xref ref-type="bibr" rid="B44">44</xref>]. Fidelis et al. [<xref ref-type="bibr" rid="B70">70</xref>] in extracts of <italic>Myrciaria dubi</italic>a have reported DPPH inhibition. <italic>Myrciaria dubia</italic>, among its main components, is mainly pedunculagin. Also, within the same genus <italic>Myrciaria cauliflora</italic> containing pedunculagin presented DPPH inhibition at higher values, as well as lipid peroxidation values, as well as lipid peroxidation values slightly greater than 80% inhibition [<xref ref-type="bibr" rid="B69">69</xref>]. Other important extracts of Jabuticaba extracts rich in vescalagin and castalagin vescalagin and castalagin showed a DPPH inhibition capacity of about 33.643 mmol ± 3.129 mmol of Tx/100 g fruit [<xref ref-type="bibr" rid="B82">82</xref>] (see <xref ref-type="table" rid="t4">Table 4</xref>).</p>
<table-wrap id="t4">
<label>Table 4</label>
<caption>
<p>Antioxidant activity of tellimagrandin I, pedunculagin, and vescalagin/castalagin</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th>
<bold>Compound</bold>
</th>
<th>
<bold>ABTS</bold>
</th>
<th>
<bold>FRAP</bold>
</th>
<th>
<bold>DPPH</bold>
</th>
<th>
<bold>Lipoperoxidation</bold>
</th>
<th>
<bold>Reference</bold>
</th>
</tr>
</thead>
<tbody>
<tr>
<td>Tellimagrandin I</td>
<td>
<bold>-</bold>
</td>
<td>-</td>
<td>-</td>
<td>51.34% ± 0.72%</td>
<td>[<xref ref-type="bibr" rid="B76">76</xref>]</td>
</tr>
<tr>
<td>Tellimagrandin I</td>
<td>255.9 mmol/100 g ± 8.48 mmol/100 g</td>
<td>210.62 mmol/100 g ± 5.45 mmol/100 g</td>
<td>191.00 mmol ± 0.04 mmol of Tx/100 g</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B74">74</xref>]</td>
</tr>
<tr>
<td>Tellimagradin I</td>
<td>
<bold>-</bold>
</td>
<td>-</td>
<td>1.45 µg/mL ± 0.02 µg/mL</td>
<td>71.47% ± 5.64%</td>
<td>[<xref ref-type="bibr" rid="B77">77</xref>]</td>
</tr>
<tr>
<td>Tellimagrandin I</td>
<td>54.5 μmol/L ± 0.6 μmol/L</td>
<td>-</td>
<td>73.5 μmol/L ± 2.5 μmol/L</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B79">79</xref>]</td>
</tr>
<tr>
<td>Tellimagrandin I</td>
<td>73.6 μmol/L ± 3.2 μmol/L</td>
<td>-</td>
<td>65.8 μmol/L ± 1.2 μmol/L</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B79">79</xref>]</td>
</tr>
<tr>
<td>Pedunculagin</td>
<td>83.69% ± 4.28% inhibition 0.111 mg/mL</td>
<td>-</td>
<td>0.139 mg/mL</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B83">83</xref>]</td>
</tr>
<tr>
<td>Tellimagrandin I</td>
<td>0.03 μmol/L ± 0.02 µmol/L Tx equivalent/µg</td>
<td>-</td>
<td>94.65% ± 0.29%</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B65">65</xref>]</td>
</tr>
<tr>
<td>Pedunculagin</td>
<td>10.8 μg/mL ± 0.7 μg/mL</td>
<td>-</td>
<td>-</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B80">80</xref>]</td>
</tr>
<tr>
<td>Vescalagin</td>
<td>
<bold>-</bold>
</td>
<td>-</td>
<td>5 mg/mL</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B44">44</xref>]</td>
</tr>
<tr>
<td>Castalagin</td>
<td>
<bold>-</bold>
</td>
<td>-</td>
<td>4 mg/mL</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B44">44</xref>]</td>
</tr>
<tr>
<td>Vescalagin/Castalagin</td>
<td>
<bold>-</bold>
</td>
<td>-</td>
<td>4,455 mg ± 15 mg AAE/100 g</td>
<td>86% ± 1%</td>
<td>[<xref ref-type="bibr" rid="B70">70</xref>]</td>
</tr>
<tr>
<td>Vescalagin/Castalagin</td>
<td>
<bold>-</bold>
</td>
<td>-</td>
<td>33.643 mmol ± 3.129 mmol of Tx/100 g</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B82">82</xref>]</td>
</tr>
<tr>
<td>Pedunculagin</td>
<td>
<bold>-</bold>
</td>
<td>-</td>
<td>1.55 µmol ± 0.12 µmol of Tx equivalent/µmol</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B37">37</xref>]</td>
</tr>
<tr>
<td>Tellimagrandin I</td>
<td>
<bold>-</bold>
</td>
<td>-</td>
<td>1.33 µmol ± 0.03 µmol of Tx equivalent/µmol</td>
<td>-</td>
<td>[<xref ref-type="bibr" rid="B37">37</xref>]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>AAE: ascorbic acid equivalent; -: not involving</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
</sec>
<sec id="s8">
<title>Future trends</title>
<p id="p-41">It is important to take into account that in plants of the <italic>Eucalyptus</italic> genus the use is oriented towards the use of EOs and compounds of these, but making use of extracts rich in ellagitannins allows them to be applied in various matrices, from supplements to functional foods for preservation or functional foods, in addition to the fact that they have provided coloration. Many of the extracts of phenolic compounds from natural sources have been mostly oriented to the pharmaceutical and cosmetic industry [<xref ref-type="bibr" rid="B84">84</xref>, <xref ref-type="bibr" rid="B85">85</xref>]. There are several studies on the use of ellagitannins in the cosmetic industry [<xref ref-type="bibr" rid="B86">86</xref>, <xref ref-type="bibr" rid="B87">87</xref>], showing their possible use in the pharmaceutical industry against cell oxidation, as well as in products aimed at cellular rejuvenation. Others have highlighted the potential use of ellagitannins in the pharmaceutical, food, and nutraceutical industries [<xref ref-type="bibr" rid="B36">36</xref>, <xref ref-type="bibr" rid="B88">88</xref>] either for its prebiotic potential [<xref ref-type="bibr" rid="B89">89</xref>], as is pedunculagin from walnuts [<xref ref-type="bibr" rid="B90">90</xref>], and for the treatment of gastric ulcers, wounds, and ulceration [<xref ref-type="bibr" rid="B39">39</xref>].</p>
<p id="p-42">However, the use of phenolic compounds such as hydrolyzable tannins, especially ellagitannins for the food industry, may be an option to solve problems such as lipid oxidation [<xref ref-type="bibr" rid="B91">91</xref>]. Pomegranate extracts with a high presence of ellagitannins have been investigated for the inhibition of lipid oxidation in sausage, where the peroxide value was decreased by the effect of pomegranate extract [<xref ref-type="bibr" rid="B92">92</xref>].</p>
<p id="p-43">Well as for the conservation against pathogenic microorganisms in food, since several studies have shown the inhibition of microorganisms in food, extracts themselves as Mantzourani et al. [<xref ref-type="bibr" rid="B93">93</xref>] with extracts from <italic>Vaccinium macrocarpon</italic> and <italic>Punica granatum</italic> L., applied on pork meat to inhibit Enterobacteriaceae, total mesophilic bacteria, yeasts/molds, <italic>Staphylococcus</italic> spp., <italic>Pseudomonas</italic> spp. and lactic acid bacteria and EOs for chicken meat preservation [<xref ref-type="bibr" rid="B91">91</xref>, <xref ref-type="bibr" rid="B94">94</xref>]. As in the case of pomegranate extract films with the presence of ellagitannins including pedunculagin, for the inhibition of microorganisms such as <italic>L. monocytogenes</italic> and <italic>E. coli</italic> [<xref ref-type="bibr" rid="B95">95</xref>]. On the other hand, extracts with ellagitannins have been shown to improve the antioxidant and meat quality of broiler meat by supplementing it, which helped to improve the intestinal bacterial population in the chicken [<xref ref-type="bibr" rid="B83">83</xref>]. In addition, the use of ellagitannins is possible in the formation of materials with antibacterial potential, such as the case of vescalagin/castalagin that can be loaded into alginate hydrogels to generate antibacterial biomaterials [<xref ref-type="bibr" rid="B44">44</xref>]. This is a step in the development of products in the food area that can aid in the inhibition of oxidation, as well as the use of antibacterial agents for the inhibition of food pathogens.</p>
</sec>
<sec id="s9">
<title>Conclusions</title>
<p id="p-44">
<italic>E. camaldulensis</italic> is a plant commonly used in industries such as wood, paper, and oil production. However, the residues of its leaves and small branches are often left unused, presenting an opportunity for utilization. This review focuses on the potential of <italic>E. camaldulensis</italic> residues particularly the phenolic compounds they contain, including hydrolyzable tannins such ellagitannins. Ellagitannins are known for their antioxidant and antimicrobial proprieties, making them valuable for various applications, specifically in the food industry for inhibiting lipid oxidation in oils and meat products. It is worth noting that there is a limited number of studies that specifically isolate ellagitannins, with most research focusing on their presence in extracts. This lack of isolated compound studies makes it challenging to gather comprehensive information about ellagitannins. Therefore, this review aims to contribute essential knowledge about these compounds and their potential uses.</p>
</sec>
</body>
<back>
<glossary>
<title>Abbreviations</title>
<def-list>
<def-item>
<term>ABTS</term>
<def>
<p>2,2-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid)</p>
</def>
</def-item>
<def-item>
<term>DPPH</term>
<def>
<p>2,2-diphenyl-1-picrylhydrazyl</p>
</def>
</def-item>
<def-item>
<term>EOs</term>
<def>
<p>essential oils</p>
</def>
</def-item>
<def-item>
<term>HHDP</term>
<def>
<p>hexahydroxy diphenic acid</p>
</def>
</def-item>
<def-item>
<term>IL-6</term>
<def>
<p>interleukin-6</p>
</def>
</def-item>
<def-item>
<term>MIC</term>
<def>
<p>minimum inhibitory concentrations</p>
</def>
</def-item>
<def-item>
<term>MRSA</term>
<def>
<p>methicillin-resistant <italic>Staphylococcus aureus</italic></p>
</def>
</def-item>
<def-item>
<term>PBP2a</term>
<def>
<p>penicillin-binding protein 2a</p>
</def>
</def-item>
<def-item>
<term>Tx</term>
<def>
<p>Trolox</p>
</def>
</def-item>
</def-list>
</glossary>
<sec id="s10">
<title>Declarations</title>
<sec>
<title>Author contributions</title>
<p>ESL: Conceptualization, Visualization, Investigation, Writing—review &amp; editing. LS: Validation, Resources, Writing—review &amp; editing. JEWP: Validation, Supervision, Writing—review &amp; editing. LPL: Validation, Writing—review &amp; editing. RRH and CNA: Validation, Supervision, Writing—review &amp; editing. JAAV: Conceptualization, Resources, Validation, Visualization, Writing—review &amp; editing.</p>
</sec>
<sec sec-type="COI-statement">
<title>Conflicts of interest</title>
<p>The authors declare that they have no conflicts of interest.</p>
</sec>
<sec>
<title>Ethical approval</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Consent to participate</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Consent to publication</title>
<p>Not applicable.</p>
</sec>
<sec sec-type="data-availability">
<title>Availability of data and materials</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Funding</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Copyright</title>
<p>© The Author(s) 2024.</p>
</sec>
</sec>
<ref-list>
<ref id="B1">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Mickymaray</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title>Efficacy and mechanism of traditional medicinal plants and bioactive compounds against clinically important pathogens</article-title>
<source>Antibiotics</source>
<year iso-8601-date="2019">2019</year>
<volume>8</volume>
<elocation-id>257</elocation-id>
<pub-id pub-id-type="doi">10.3390/antibiotics8040257</pub-id><pub-id pub-id-type="pmid">31835403</pub-id><pub-id pub-id-type="pmcid">PMC6963422</pub-id></element-citation>
</ref>
<ref id="B2">
<label>2</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Knezevic</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Aleksic</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Simin</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Svircev</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Petrovic</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Mimica-Dukic</surname>
<given-names>N</given-names>
</name>
</person-group>
<article-title>Antimicrobial activity of <italic>Eucalyptus camaldulensis</italic> essential oils and their interactions with conventional antimicrobial agents against multi-drug resistant <italic>Acinetobacter baumannii</italic></article-title>
<source>J Ethnopharmacol</source>
<year iso-8601-date="2016">2016</year>
<volume>178</volume>
<fpage>125</fpage>
<lpage>36</lpage>
<pub-id pub-id-type="doi">10.1016/j.jep.2015.12.008</pub-id><pub-id pub-id-type="pmid">26671210</pub-id></element-citation>
</ref>
<ref id="B3">
<label>3</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Kayani</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Ahmad</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Zafar</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Sultana</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Khan</surname>
<given-names>MPZ</given-names>
</name>
<name>
<surname>Ashraf</surname>
<given-names>MA</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Ethnobotanical uses of medicinal plants for respiratory disorders among the inhabitants of Gallies-Abbottabad, Northern Pakistan</article-title>
<source>J Ethnopharmacol</source>
<year iso-8601-date="2014">2014</year>
<volume>156</volume>
<fpage>47</fpage>
<lpage>60</lpage>
<pub-id pub-id-type="doi">10.1016/j.jep.2014.08.005</pub-id><pub-id pub-id-type="pmid">25153021</pub-id></element-citation>
</ref>
<ref id="B4">
<label>4</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Zurita</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Posligua</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Mora</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Carranza</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Bacusoy</surname>
<given-names>M</given-names>
</name>
</person-group>
<article-title>Plantas medicinales, su uso en afecciones respiratorias en comunidades rurales, provincia Los Ríos-Ecuador</article-title>
<source>J Sci Res</source>
<year iso-8601-date="2021">2021</year>
<volume>6</volume>
<fpage>57</fpage>
<lpage>72. Spanish</lpage>
</element-citation>
</ref>
<ref id="B5">
<label>5</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Dhakad</surname>
<given-names>AK</given-names>
</name>
<name>
<surname>Pandey</surname>
<given-names>VV</given-names>
</name>
<name>
<surname>Beg</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Rawat</surname>
<given-names>JM</given-names>
</name>
<name>
<surname>Singh</surname>
<given-names>A</given-names>
</name>
</person-group>
<article-title>Biological, medicinal and toxicological significance of <italic>Eucalyptus</italic> leaf essential oil: a review</article-title>
<source>J Sci Food Agri</source>
<year iso-8601-date="2018">2018</year>
<volume>98</volume>
<fpage>833</fpage>
<lpage>48</lpage>
<pub-id pub-id-type="doi">10.1002/jsfa.8600</pub-id><pub-id pub-id-type="pmid">28758221</pub-id></element-citation>
</ref>
<ref id="B6">
<label>6</label>
<element-citation publication-type="book">
<person-group person-group-type="author">
<name>
<surname>Labate</surname>
<given-names>CA</given-names>
</name>
<name>
<surname>de Assis</surname>
<given-names>TF</given-names>
</name>
<name>
<surname>Oda</surname>
<given-names>S</given-names>
</name>
<name>
<surname>de Mello</surname>
<given-names>EJ</given-names>
</name>
<name>
<surname>Mori</surname>
<given-names>ES</given-names>
</name>
<name>
<surname>de Moraes</surname>
<given-names>MLT</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Eucalyptus</article-title>
<person-group person-group-type="editor">
<name>
<surname>Kole</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Hall</surname>
<given-names>TC</given-names>
</name>
</person-group>
<source>Compendium of transgenic crop plants</source>
<comment>Blackwell Publishing Ltd; 2008. pp. 35–108</comment>
</element-citation>
</ref>
<ref id="B7">
<label>7</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Lee</surname>
<given-names>MH</given-names>
</name>
</person-group>
<article-title>Chemical profile, antimicrobial and anti-oxidative activity of commercial eucalyptus and lavender essential oils and their applicability in cosmetics</article-title>
<source>Indian J Sci Technol</source>
<year iso-8601-date="2016">2016</year>
<volume>9</volume>
<elocation-id>100181106</elocation-id>
<pub-id pub-id-type="doi">10.17485/ijst/2016/v9i46/107856</pub-id></element-citation>
</ref>
<ref id="B8">
<label>8</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Sharmeen</surname>
<given-names>JB</given-names>
</name>
<name>
<surname>Mahomoodally</surname>
<given-names>FM</given-names>
</name>
<name>
<surname>Zengin</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Maggi</surname>
<given-names>F</given-names>
</name>
</person-group>
<article-title>Essential oils as natural sources of fragrance compounds for cosmetics and cosmeceuticals</article-title>
<source>Molecules</source>
<year iso-8601-date="2021">2021</year>
<volume>26</volume>
<elocation-id>666</elocation-id>
<pub-id pub-id-type="doi">10.3390/molecules26030666</pub-id><pub-id pub-id-type="pmid">33514008</pub-id><pub-id pub-id-type="pmcid">PMC7865210</pub-id></element-citation>
</ref>
<ref id="B9">
<label>9</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Becker</surname>
<given-names>LC</given-names>
</name>
<name>
<surname>Akinsulie</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Bergfeld</surname>
<given-names>WF</given-names>
</name>
<name>
<surname>Belsito</surname>
<given-names>DV</given-names>
</name>
<name>
<surname>Hill</surname>
<given-names>RA</given-names>
</name>
<name>
<surname>Klaassen</surname>
<given-names>CD</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Safety assessment of <italic>Eucalyptus globulus</italic> (Eucalyptus)-derived ingredients as used in cosmetics</article-title>
<source>Int J Toxicol</source>
<year iso-8601-date="2023">2023</year>
<volume>42</volume>
<fpage>57S</fpage>
<lpage>92S</lpage>
<pub-id pub-id-type="doi">10.1177/10915818231164354</pub-id></element-citation>
</ref>
<ref id="B10">
<label>10</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Tolba</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Moghrani</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Benelmouffok</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Kellou</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Maachi</surname>
<given-names>R</given-names>
</name>
</person-group>
<article-title>Essential oil of Algerian <italic>Eucalyptus citriodora</italic>: chemical composition, antifungal activity</article-title>
<source>J Mycol Med.</source>
<year iso-8601-date="2015">2015</year>
<volume>25</volume>
<fpage>e128</fpage>
<lpage>33</lpage>
<pub-id pub-id-type="doi">10.1016/j.mycmed.2015.10.009</pub-id><pub-id pub-id-type="pmid">26597375</pub-id></element-citation>
</ref>
<ref id="B11">
<label>11</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Nwabor</surname>
<given-names>OF</given-names>
</name>
<name>
<surname>Singh</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Syukri</surname>
<given-names>DM</given-names>
</name>
<name>
<surname>Voravuthikunchai</surname>
<given-names>SP</given-names>
</name>
</person-group>
<article-title>Bioactive fractions of <italic>Eucalyptus</italic> camaldulensis inhibit important foodborne pathogens, reduce listeriolysin O-induced haemolysis, and ameliorate hydrogen peroxide-induced oxidative stress on human embryonic colon cells</article-title>
<source>Food Chem.</source>
<year iso-8601-date="2021">2021</year>
<volume>344</volume>
<elocation-id>128571</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.foodchem.2020.128571</pub-id><pub-id pub-id-type="pmid">33221106</pub-id></element-citation>
</ref>
<ref id="B12">
<label>12</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Huang</surname>
<given-names>Q</given-names>
</name>
<name>
<surname>Liu</surname>
<given-names>X</given-names>
</name>
<name>
<surname>Zhao</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Hu</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Wang</surname>
<given-names>Y</given-names>
</name>
</person-group>
<article-title>Potential and challenges of tannins as an alternative to in-feed antibiotics for farm animal production</article-title>
<source>Anim Nutr.</source>
<year iso-8601-date="2018">2018</year>
<volume>4</volume>
<fpage>137</fpage>
<lpage>50</lpage>
<pub-id pub-id-type="doi">10.1016/j.aninu.2017.09.004</pub-id><pub-id pub-id-type="pmid">30140753</pub-id><pub-id pub-id-type="pmcid">PMC6104569</pub-id></element-citation>
</ref>
<ref id="B13">
<label>13</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Panamito</surname>
<given-names>MF</given-names>
</name>
<name>
<surname>Bec</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Valdivieso</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Salinas</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Calva</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Ramírez</surname>
<given-names>J</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Chemical composition and anticholinesterase activity of the essential oil of leaves and flowers from the ecuadorian plant <italic>Lepechinia paniculata</italic> (Kunth) epling</article-title>
<source>Molecules</source>
<year iso-8601-date="2021">2021</year>
<volume>26</volume>
<elocation-id>3198</elocation-id>
<pub-id pub-id-type="doi">10.3390/molecules26113198</pub-id><pub-id pub-id-type="pmid">34071744</pub-id><pub-id pub-id-type="pmcid">PMC8199004</pub-id></element-citation>
</ref>
<ref id="B14">
<label>14</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Aleksic</surname>
<given-names>Sabo V</given-names>
</name>
<name>
<surname>Knezevic</surname>
<given-names>P</given-names>
</name>
</person-group>
<article-title>Antimicrobial activity of <italic>Eucalyptus camaldulensis</italic> Dehn. plant extracts and essential oils: a review</article-title>
<source>Ind Crops Prod</source>
<year iso-8601-date="2019">2019</year>
<volume>132</volume>
<fpage>413</fpage>
<lpage>29</lpage>
<pub-id pub-id-type="doi">10.1016/j.indcrop.2019.02.051</pub-id><pub-id pub-id-type="pmid">32288268</pub-id><pub-id pub-id-type="pmcid">PMC7126574</pub-id></element-citation>
</ref>
<ref id="B15">
<label>15</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Al-Snafi</surname>
<given-names>PDAE</given-names>
</name>
</person-group>
<article-title>The pharmacological and therapeutic importance of Eucalyptus species grown in Iraq</article-title>
<source>IOSR J Pharm</source>
<year iso-8601-date="2017">2017</year>
<volume>7</volume>
<fpage>72</fpage>
<lpage>91</lpage>
<pub-id pub-id-type="doi">10.9790/3013-0703017291</pub-id></element-citation>
</ref>
<ref id="B16">
<label>16</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Yáñez</surname>
<given-names>Rueda X</given-names>
</name>
<name>
<surname>Cuadro</surname>
<given-names>Mogollón OF</given-names>
</name>
</person-group>
<article-title>Composición química y actividad antibacteriana del aceite esencial de las especies <italic>Eucalyptus globulus</italic> y E. camaldulensis de tres zonas de Pamplona (Colombia)</article-title>
<source>Bioagro</source>
<year iso-8601-date="2012">2012</year>
<volume>10</volume>
<fpage>52</fpage>
<lpage>61. Spanish</lpage>
</element-citation>
</ref>
<ref id="B17">
<label>17</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Singa</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Ayoub</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Al-Sayed</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Martiskainen</surname>
<given-names>O</given-names>
</name>
<name>
<surname>Sinkkonen</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Pihlaja</surname>
<given-names>K</given-names>
</name>
</person-group>
<article-title>Phenolic constituents of <italic>Eucalyptus camaldulensis</italic> Dehnh, with potential antioxidant and cytotoxic activities</article-title>
<source>Rec Nat Prod</source>
<year iso-8601-date="2011">2011</year>
<volume>5</volume>
<fpage>271</fpage>
<lpage>80</lpage>
</element-citation>
</ref>
<ref id="B18">
<label>18</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>González-González</surname>
<given-names>GM</given-names>
</name>
<name>
<surname>Palomo-Ligas</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Nery-Flores</surname>
<given-names>SD</given-names>
</name>
<name>
<surname>Ascacio-Valdés</surname>
<given-names>JA</given-names>
</name>
<name>
<surname>Sáenz-Galindo</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Flores-Gallegos</surname>
<given-names>AC</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Coffee pulp as a source for polyphenols extraction using ultrasound, microwave, and green solvents</article-title>
<source>Environ Qual Manag</source>
<year iso-8601-date="2022">2022</year>
<volume>32</volume>
<fpage>451</fpage>
<lpage>61</lpage>
<pub-id pub-id-type="doi">10.1002/tqem.21903</pub-id></element-citation>
</ref>
<ref id="B19">
<label>19</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Doganlar</surname>
<given-names>ZB</given-names>
</name>
<name>
<surname>Doganlar</surname>
<given-names>O</given-names>
</name>
<name>
<surname>Erdogan</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Onal</surname>
<given-names>Y</given-names>
</name>
</person-group>
<article-title>Heavy metal pollution and physiological changes in the leaves of some shrub, palm and tree species in urban areas of Adana, Turkey</article-title>
<source>Chem Speciat Bioavailab</source>
<year iso-8601-date="2012">2012</year>
<volume>24</volume>
<fpage>65</fpage>
<lpage>78</lpage>
<pub-id pub-id-type="doi">10.3184/095422912X13338055043100</pub-id></element-citation>
</ref>
<ref id="B20">
<label>20</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Kanda</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Ncube</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Goronga</surname>
<given-names>TK</given-names>
</name>
</person-group>
<article-title>Trace elements in leaf extracts of <italic>Eucalyptus grandis</italic> traditionally used to treat common cold and flu</article-title>
<source>J Heal Pollut</source>
<year iso-8601-date="2019">2019</year>
<volume>9</volume>
<elocation-id>191214</elocation-id>
<pub-id pub-id-type="doi">10.5696/2156-9614-9.24.191214</pub-id><pub-id pub-id-type="pmid">31893175</pub-id><pub-id pub-id-type="pmcid">PMC6905133</pub-id></element-citation>
</ref>
<ref id="B21">
<label>21</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Aljawdah</surname>
<given-names>HMA</given-names>
</name>
<name>
<surname>Abdel-Gaber</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Al-Shaebi</surname>
<given-names>EM</given-names>
</name>
<name>
<surname>Thagfan</surname>
<given-names>FA</given-names>
</name>
<name>
<surname>Al-Quraishy</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Qasem</surname>
<given-names>MAA</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Hepatoprotective activity of <italic>Eucalyptus camaldulensis</italic> extract in murine malaria mediated by suppression of oxidative and inflammatory processes</article-title>
<source>Front Cell Infect Microbiol</source>
<year iso-8601-date="2022">2022</year>
<volume>12</volume>
<elocation-id>955042</elocation-id>
<pub-id pub-id-type="doi">10.3389/fcimb.2022.955042</pub-id><pub-id pub-id-type="pmid">36034714</pub-id><pub-id pub-id-type="pmcid">PMC9412018</pub-id></element-citation>
</ref>
<ref id="B22">
<label>22</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Roy</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Khan</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Ahmad</surname>
<given-names>I</given-names>
</name>
<name>
<surname>Alghamdi</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Rajab</surname>
<given-names>BS</given-names>
</name>
<name>
<surname>Babalghith</surname>
<given-names>AO</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Flavonoids a bioactive compound from medicinal plants and its therapeutic applications</article-title>
<source>Biomed Res Int</source>
<year iso-8601-date="2022">2022</year>
<volume>2022</volume>
<elocation-id>5445291</elocation-id>
<pub-id pub-id-type="doi">10.1155/2022/5445291</pub-id><pub-id pub-id-type="pmid">35707379</pub-id><pub-id pub-id-type="pmcid">PMC9192232</pub-id></element-citation>
</ref>
<ref id="B23">
<label>23</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Abbas</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Anwar</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Alqahtani</surname>
<given-names>SM</given-names>
</name>
<name>
<surname>Ahmad</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Al-Mijalli</surname>
<given-names>SH</given-names>
</name>
<name>
<surname>Shahid</surname>
<given-names>M</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Hydro-distilled and supercritical fluid extraction of <italic>Eucalyptus camaldulensis</italic> essential oil: characterization of bioactives along with antioxidant, antimicrobial and antibiofilm activities</article-title>
<source>Dose-Response</source>
<year iso-8601-date="2022">2022</year>
<volume>20</volume>
<elocation-id>15593258221125477</elocation-id>
<pub-id pub-id-type="doi">10.1177/15593258221125477</pub-id><pub-id pub-id-type="pmid">36106059</pub-id><pub-id pub-id-type="pmcid">PMC9465602</pub-id></element-citation>
</ref>
<ref id="B24">
<label>24</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Masyita</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Mustika</surname>
<given-names>Sari R</given-names>
</name>
<name>
<surname>Dwi</surname>
<given-names>Astuti A</given-names>
</name>
<name>
<surname>Yasir</surname>
<given-names>B</given-names>
</name>
<name>
<surname>Rahma</surname>
<given-names>Rumata N</given-names>
</name>
<name>
<surname>Emran</surname>
<given-names>TB</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Terpenes and terpenoids as main bioactive compounds of essential oils, their roles in human health and potential application as natural food preservatives</article-title>
<source>Food Chem X</source>
<year iso-8601-date="2022">2022</year>
<volume>13</volume>
<elocation-id>100217</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.fochx.2022.100217</pub-id><pub-id pub-id-type="pmid">35498985</pub-id><pub-id pub-id-type="pmcid">PMC9039924</pub-id></element-citation>
</ref>
<ref id="B25">
<label>25</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Conde</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Cadahía</surname>
<given-names>E</given-names>
</name>
<name>
<surname>García-Vallejo</surname>
<given-names>MC</given-names>
</name>
</person-group>
<article-title>Low molecular weight polyphenols in leaves of <italic>Eucalyptus camaldulensis</italic>, <italic>E. globulusandE. rudis</italic></article-title>
<source>Phytochem Anal</source>
<year iso-8601-date="1997">1997</year>
<volume>8</volume>
<fpage>186</fpage>
<lpage>93</lpage>
<pub-id pub-id-type="doi">10.1002/(SICI)1099-1565(199707)8:4&lt;186::AID-PCA355&gt;2-7</pub-id></element-citation>
</ref>
<ref id="B26">
<label>26</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Cadahía</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Conde</surname>
<given-names>E</given-names>
</name>
<name>
<surname>García-vallejo</surname>
<given-names>MC</given-names>
</name>
<name>
<surname>Fernández</surname>
<given-names>de Simón B</given-names>
</name>
</person-group>
<article-title>High pressure liquid chromatographic analysis of polyphenols in leaves of <italic>Eucalyptus camaldulensis, E. globulus</italic> and<italic> E. rudis</italic>:  proanthocyanidins, ellagitannins and flavonol glycosides</article-title>
<source>Phytochem Anal</source>
<year iso-8601-date="1997">1997</year>
<volume>8</volume>
<fpage>78</fpage>
<lpage>83</lpage>
<pub-id pub-id-type="doi">10.1002/(SICI)1099-1565(199703)8:2&lt;78::AID-PCA335&gt;3.0.CO;2-O</pub-id></element-citation>
</ref>
<ref id="B27">
<label>27</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Radwan</surname>
<given-names>RA</given-names>
</name>
<name>
<surname>El-sherif</surname>
<given-names>YA</given-names>
</name>
<name>
<surname>Salama</surname>
<given-names>MM</given-names>
</name>
</person-group>
<article-title>A novel biochemical study of anti-ageing potential of <italic>Eucalyptus Camaldulensis</italic> bark waste standardized extract and silver nanoparticles</article-title>
<source>Colloids Surfaces B Biointerfaces</source>
<year iso-8601-date="2020">2020</year>
<volume>191</volume>
<elocation-id>111004</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.colsurfb.2020.111004</pub-id><pub-id pub-id-type="pmid">32335357</pub-id></element-citation>
</ref>
<ref id="B28">
<label>28</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Conde</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Wood</surname>
<given-names>E</given-names>
</name>
</person-group>
<article-title>Polyphenolic composition of wood extracts from <italic>Eucalyptus camaldulensis</italic>, <italic>E. globulus</italic> and <italic>E.</italic> rudis</article-title>
<source>Holzforschung</source>
<year iso-8601-date="1995">1995</year>
<volume>49</volume>
<fpage>411</fpage>
<lpage>7</lpage>
<pub-id pub-id-type="doi">10.1515/hfsg.1995.49.5.411</pub-id></element-citation>
</ref>
<ref id="B29">
<label>29</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Banks</surname>
<given-names>JCG</given-names>
</name>
<name>
<surname>Hillis</surname>
<given-names>WE</given-names>
</name>
</person-group>
<article-title>The characterization of populations of <italic>Eucalyptus camaldulensis</italic> by chemical features</article-title>
<source>Aust. J. Bot</source>
<year iso-8601-date="1963">1963</year>
<volume>17</volume>
<fpage>133</fpage>
<lpage>46</lpage>
<pub-id pub-id-type="doi">10.1071/BT9690133</pub-id></element-citation>
</ref>
<ref id="B30">
<label>30</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Buenrostro-Figueroa</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Ascacio-Valdés</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Sepúlveda</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Prado-Barragán</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Aguilar-González</surname>
<given-names>MÁ</given-names>
</name>
<name>
<surname>Aguilar</surname>
<given-names>CN</given-names>
</name>
</person-group>
<article-title>Ellagic acid production by solid-state fermentation influenced by the inert solid supports</article-title>
<source>Emirates J Food Agric</source>
<year iso-8601-date="2018">2018</year>
<volume>30</volume>
<fpage>750</fpage>
<lpage>7</lpage>
<pub-id pub-id-type="doi">10.9755/EJFA.2018.V30.I9.1796</pub-id></element-citation>
</ref>
<ref id="B31">
<label>31</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Márquez</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Chavéz</surname>
<given-names>C</given-names>
</name>
<name>
<surname>González</surname>
<given-names>J</given-names>
</name>
</person-group>
<article-title>Aspectos generales sobre los elagitaninos y su conversión a ácido elágico</article-title>
<source>Ciencia Nicolaita</source>
<year iso-8601-date="2019">2019</year>
<fpage>36</fpage>
<lpage>58. Spanish</lpage>
</element-citation>
</ref>
<ref id="B32">
<label>32</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Enomoto</surname>
<given-names>H</given-names>
</name>
</person-group>
<article-title>Unique distribution of ellagitannins in ripe strawberry fruit revealed by mass spectrometry imaging</article-title>
<source>Curr Res Food Sci</source>
<year iso-8601-date="2021">2021</year>
<volume>4</volume>
<fpage>821</fpage>
<lpage>8</lpage>
<pub-id pub-id-type="doi">10.1016/j.crfs.2021.11.006</pub-id><pub-id pub-id-type="pmid">34841268</pub-id><pub-id pub-id-type="pmcid">PMC8606305</pub-id></element-citation>
</ref>
<ref id="B33">
<label>33</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Nandasiri</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Eskin</surname>
<given-names>NAM</given-names>
</name>
<name>
<surname>Thiyam-Höllander</surname>
<given-names>U</given-names>
</name>
</person-group>
<article-title>Antioxidative polyphenols of canola meal extracted by high pressure: impact of temperature and solvents</article-title>
<source>J Food Sci</source>
<year iso-8601-date="2019">2019</year>
<volume>84</volume>
<fpage>3117</fpage>
<lpage>28</lpage>
<pub-id pub-id-type="doi">10.1111/1750-3841.14799</pub-id><pub-id pub-id-type="pmid">31663155</pub-id></element-citation>
</ref>
<ref id="B34">
<label>34</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>El</surname>
<given-names>Achkar T</given-names>
</name>
<name>
<surname>Fourmentin</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Greige-Gerges</surname>
<given-names>H</given-names>
</name>
</person-group>
<article-title>Deep eutectic solvents: an overview on their interactions with water and biochemical compounds</article-title>
<source>J Mol Liq</source>
<year iso-8601-date="2019">2019</year>
<volume>288</volume>
<elocation-id>15:111028</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.molliq.2019.111028</pub-id></element-citation>
</ref>
<ref id="B35">
<label>35</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Hernandez-Trejo</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Rodríguez-Herrera</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Sáenz-Galindo</surname>
<given-names>A</given-names>
</name>
<name>
<surname>López-Badillo</surname>
<given-names>CM</given-names>
</name>
<name>
<surname>Flores-Gallegos</surname>
<given-names>AC</given-names>
</name>
<name>
<surname>Ascacio-Valdez</surname>
<given-names>JA</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Insecticidal capacity of polyphenolic seed compounds from neem (<italic>Azadirachta indica</italic>) on <italic>Spodoptera frugiperda</italic> (J. E. Smith) larvae</article-title>
<source>J Environ Sci Health Bi</source>
<year iso-8601-date="2021">2021</year>
<volume>56</volume>
<fpage>1023</fpage>
<lpage>30</lpage>
<pub-id pub-id-type="doi">10.1080/03601234.2021.2004853</pub-id><pub-id pub-id-type="pmid">34783634</pub-id></element-citation>
</ref>
<ref id="B36">
<label>36</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Sugimoto</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Nakagawa</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Hayashi</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Amakura</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Yoshimura</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Yoshida</surname>
<given-names>T</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Hydrolyzable tannins as antioxidants in the leaf extract of eucalyptus globulus possessing tyrosinase and hyaluronidase inhibitory activities</article-title>
<source>Food Sci Technol Res</source>
<year iso-8601-date="2009">2009</year>
<volume>15</volume>
<fpage>331</fpage>
<lpage>6</lpage>
<pub-id pub-id-type="doi">10.3136/fstr.15.331</pub-id></element-citation>
</ref>
<ref id="B37">
<label>37</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Santos</surname>
<given-names>SC</given-names>
</name>
<name>
<surname>Fortes</surname>
</name>
<name>
<surname>Gilmara</surname>
<given-names>ACF</given-names>
</name>
<name>
<surname>Camargo</surname>
<given-names>LTFM</given-names>
</name>
<name>
<surname>Camargo</surname>
<given-names>AJ</given-names>
</name>
<name>
<surname>Ferri</surname>
<given-names>PH</given-names>
</name>
</person-group>
<article-title>Antioxidant effects of polyphenolic compounds and structure-activity relationship predicted by multivariate regression tree</article-title>
<source>LWT</source>
<year iso-8601-date="2020">2020</year>
<volume>137</volume>
<elocation-id>110366</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.lwt.2020.110366</pub-id></element-citation>
</ref>
<ref id="B38">
<label>38</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Barry</surname>
<given-names>KM</given-names>
</name>
<name>
<surname>Davies</surname>
<given-names>NW</given-names>
</name>
<name>
<surname>Mohammed</surname>
<given-names>CL</given-names>
</name>
</person-group>
<article-title>Identification of hydrolysable tannins in the reaction zone of <italic>Eucalyptus nitens</italic> wood by high performance liquid chromatography–electrospray ionisation mass spectrometry</article-title>
<source>Phytochem Anal</source>
<year iso-8601-date="2001">2001</year>
<volume>12</volume>
<fpage>120</fpage>
<lpage>7</lpage>
<pub-id pub-id-type="doi">10.1002/pca.548</pub-id><pub-id pub-id-type="pmid">11705240</pub-id></element-citation>
</ref>
<ref id="B39">
<label>39</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Al-Sayed</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Michel</surname>
<given-names>HE</given-names>
</name>
<name>
<surname>Khattab</surname>
<given-names>MA</given-names>
</name>
<name>
<surname>El-Shazly</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Singab</surname>
<given-names>AN</given-names>
</name>
</person-group>
<article-title>Protective role of casuarinin from melaleuca leucadendra against ethanol-induced gastric ulcer in rats</article-title>
<source>Planta Med</source>
<year iso-8601-date="2020">2020</year>
<volume>86</volume>
<fpage>32</fpage>
<lpage>44</lpage>
<pub-id pub-id-type="doi">10.1055/a-1031-7328</pub-id><pub-id pub-id-type="pmid">31689719</pub-id></element-citation>
</ref>
<ref id="B40">
<label>40</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Zhang</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Zhu</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Zhang</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>He</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Wang</surname>
<given-names>Q</given-names>
</name>
</person-group>
<article-title>Simultaneous detection of three foodborne pathogenic bacteria in food samples by microchip capillary electrophoresis in combination with polymerase chain reaction</article-title>
<source>J Chromatogr A</source>
<year iso-8601-date="2018">2018</year>
<volume>1555</volume>
<fpage>100</fpage>
<lpage>5</lpage>
<pub-id pub-id-type="doi">10.1016/j.chroma.2018.04.058</pub-id><pub-id pub-id-type="pmid">29724645</pub-id></element-citation>
</ref>
<ref id="B41">
<label>41</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Bintsis</surname>
<given-names>T</given-names>
</name>
</person-group>
<article-title>Foodborne pathogens</article-title>
<source>AIMS Microbiol</source>
<year iso-8601-date="2017">2017</year>
<volume>3</volume>
<fpage>529</fpage>
<lpage>63</lpage>
<pub-id pub-id-type="doi">10.3934/microbiol.2017.3.529</pub-id></element-citation>
</ref>
<ref id="B42">
<label>42</label>
<element-citation publication-type="book">
<person-group person-group-type="author">
<name>
<surname>Gourama</surname>
<given-names>H</given-names>
</name>
</person-group>
<article-title>Foodborne pathogens</article-title>
<person-group person-group-type="editor">
<name>
<surname>Barbosa-Cánovas</surname>
<given-names>GV</given-names>
</name>
</person-group>
<source>Food engineering series</source>
<publisher-loc>New York</publisher-loc>
<publisher-name>Springer</publisher-name>
<year iso-8601-date="2020">2020</year>
<comment>pp. 25–49.</comment>
</element-citation>
</ref>
<ref id="B43">
<label>43</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Adebowale</surname>
<given-names>OO</given-names>
</name>
<name>
<surname>Kassim</surname>
<given-names>IO</given-names>
</name>
</person-group>
<article-title>Food safety and health: a survey of rural and urban household consumer practices, knowledge to food safety and food related illnesses in Ogun state</article-title>
<source>Epidemiol Biostat Public Heal</source>
<year iso-8601-date="2017">2017</year>
<volume>14</volume>
<elocation-id>e12568</elocation-id>
<pub-id pub-id-type="doi">10.2427/12568</pub-id></element-citation>
</ref>
<ref id="B44">
<label>44</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Araújo</surname>
<given-names>AR</given-names>
</name>
<name>
<surname>Araújo</surname>
<given-names>AC</given-names>
</name>
<name>
<surname>Reis</surname>
<given-names>RL</given-names>
</name>
<name>
<surname>Pires</surname>
<given-names>RA</given-names>
</name>
</person-group>
<article-title>Vescalagin and castalagin present bactericidal activity toward methicillin-resistant bacteria</article-title>
<source>ACS Biomater Sci Eng</source>
<year iso-8601-date="2021">2021</year>
<volume>7</volume>
<fpage>1022</fpage>
<lpage>30</lpage>
<pub-id pub-id-type="doi">10.1021/acsbiomaterials.0c01698</pub-id><pub-id pub-id-type="pmid">33596039</pub-id></element-citation>
</ref>
<ref id="B45">
<label>45</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Ghalem</surname>
<given-names>BR</given-names>
</name>
<name>
<surname>Mohamed</surname>
<given-names>B</given-names>
</name>
</person-group>
<article-title>Antibacterial activity of leaf essential oils of <italic>Eucalyptus globulus</italic> and <italic>Eucalyptus camaldulensis</italic></article-title>
<source>African J Pharm Pharmacol</source>
<year iso-8601-date="2008">2008</year>
<volume>2</volume>
<fpage>211</fpage>
<lpage>5</lpage>
</element-citation>
</ref>
<ref id="B46">
<label>46</label>
<element-citation publication-type="book">
<person-group person-group-type="author">
<name>
<surname>Quideau</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title>Chemistry and biology of ellagitannins</article-title>
<person-group person-group-type="editor">
<name>
<surname>Quideau</surname>
<given-names>S</given-names>
</name>
</person-group>
<source>An underestimated class of bioactive plant polyohenols</source>
<publisher-loc>Hackensack</publisher-loc>
<publisher-name>World Scientific</publisher-name>
<year iso-8601-date="2009">2009</year>
<comment>p. 396.</comment>
</element-citation>
</ref>
<ref id="B47">
<label>47</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Zheng</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Laraia</surname>
<given-names>L</given-names>
</name>
<name>
<surname>O’Connor</surname>
<given-names>CJ</given-names>
</name>
<name>
<surname>Sorrell</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Tan</surname>
<given-names>YS</given-names>
</name>
<name>
<surname>Xu</surname>
<given-names>Z</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Synthesis and biological profiling of tellimagrandin I and analogues reveals that the medium ring can significantly modulate biological activity</article-title>
<source>Org Biomol Chem</source>
<year iso-8601-date="2012">2012</year>
<volume>10</volume>
<fpage>2590</fpage>
<lpage>3</lpage>
<pub-id pub-id-type="doi">10.1039/c2ob25065a</pub-id><pub-id pub-id-type="pmid">22361895</pub-id></element-citation>
</ref>
<ref id="B48">
<label>48</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Salih</surname>
<given-names>EYA</given-names>
</name>
<name>
<surname>Julkunen-Tiitto</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Luukkanen</surname>
<given-names>O</given-names>
</name>
<name>
<surname>Fahmi</surname>
<given-names>MKM</given-names>
</name>
<name>
<surname>Fyhrquist</surname>
<given-names>P</given-names>
</name>
</person-group>
<article-title>Hydrolyzable tannins (ellagitannins), flavonoids, pentacyclic triterpenes and their glycosides in antimycobacterial extracts of the ethnopharmacologically selected Sudanese medicinal plant <italic>Combretum hartmannianum</italic> schweinf</article-title>
<source>Biomed Pharmacother</source>
<year iso-8601-date="2021">2021</year>
<volume>144</volume>
<elocation-id>112264</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.biopha.2021.112264</pub-id><pub-id pub-id-type="pmid">34624680</pub-id></element-citation>
</ref>
<ref id="B49">
<label>49</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Puljula</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Walton</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Woodward</surname>
<given-names>MJ</given-names>
</name>
<name>
<surname>Karonen</surname>
<given-names>M</given-names>
</name>
</person-group>
<article-title>Antimicrobial activities of ellagitannins against clostridiales <italic>perfringens</italic>, <italic>Escherichia coli</italic>, <italic>Lactobacillus plantarum</italic> and <italic>Staphylococcus aureus</italic></article-title>
<source>Molecules</source>
<year iso-8601-date="2020">2020</year>
<volume>25</volume>
<elocation-id>3714</elocation-id>
<pub-id pub-id-type="doi">10.3390/molecules25163714</pub-id><pub-id pub-id-type="pmid">32824081</pub-id><pub-id pub-id-type="pmcid">PMC7465317</pub-id></element-citation>
</ref>
<ref id="B50">
<label>50</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Shiota</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Shimizu</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Mizusima</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Ito</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Hatano</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Yoshida</surname>
<given-names>T</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Restoration of effectiveness of β-lactams on methicillin-resistant <italic>Staphylococcus aureus</italic> by tellimagrandin I from rose red</article-title>
<source>FEMS Microbiol Lett</source>
<year iso-8601-date="2000">2000</year>
<volume>185</volume>
<fpage>135</fpage>
<lpage>8</lpage>
<pub-id pub-id-type="doi">10.1111/j.1574-6968.2000.tb09051.x</pub-id><pub-id pub-id-type="pmid">10754237</pub-id></element-citation>
</ref>
<ref id="B51">
<label>51</label>
<element-citation publication-type="book">
<person-group person-group-type="author">
<name>
<surname>Grace</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Fetsch</surname>
<given-names>A</given-names>
</name>
</person-group>
<article-title>
<italic>Staphylococcus aureus</italic>—a foodborne pathogen: epidemiology, detection, characterization, prevention, and control: an overview</article-title>
<person-group person-group-type="editor">
<name>
<surname>Fetsch</surname>
<given-names>A</given-names>
</name>
</person-group>
<source>Staphylococcus aureus</source>
<comment>Elsevier Inc; 2018. pp. 3–10.</comment>
</element-citation>
</ref>
<ref id="B52">
<label>52</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Zendejas-Manzo</surname>
<given-names>GS</given-names>
</name>
<name>
<surname>Avalos-Flores</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Soto-Padilla</surname>
<given-names>MY</given-names>
</name>
</person-group>
<article-title>Microbiología general de <italic>Staphylococcus aureus</italic>: generalidades, patogenicidad y métodos de identificación</article-title>
<source>Rev Biomed</source>
<year iso-8601-date="2014">2014</year>
<volume>25</volume>
<fpage>129</fpage>
<lpage>43</lpage>
</element-citation>
</ref>
<ref id="B53">
<label>53</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Funatogawa</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Hayashi</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Shimomura</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Yoshida</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Hatano</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Ito</surname>
<given-names>H</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Antibacterial activity of hydrolyzable tannins derived from medicinal plants against <italic>Helicobacter pylori</italic></article-title>
<source>Microbiol Immunol</source>
<year iso-8601-date="2004">2004</year>
<volume>48</volume>
<fpage>251</fpage>
<lpage>61</lpage>
<pub-id pub-id-type="doi">10.1111/j.1348-0421.2004.tb03521.x</pub-id><pub-id pub-id-type="pmid">15107535</pub-id></element-citation>
</ref>
<ref id="B54">
<label>54</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Hou</surname>
<given-names>AJ</given-names>
</name>
<name>
<surname>Liu</surname>
<given-names>YZ</given-names>
</name>
<name>
<surname>Yang</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Lin</surname>
<given-names>ZW</given-names>
</name>
<name>
<surname>Sun</surname>
<given-names>HD</given-names>
</name>
</person-group>
<article-title>Hydrolyzable tannins and related polyphenols from <italic>Eucalyptus globulus</italic></article-title>
<source>J Asian Nat Prod Res</source>
<year iso-8601-date="2000">2000</year>
<volume>2</volume>
<fpage>205</fpage>
<lpage>12</lpage>
<pub-id pub-id-type="doi">10.1080/10286020008039912</pub-id><pub-id pub-id-type="pmid">11256694</pub-id></element-citation>
</ref>
<ref id="B55">
<label>55</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Boulekbache-Makhlouf</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Slimani</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Madani</surname>
<given-names>K</given-names>
</name>
</person-group>
<article-title>Total phenolic content, antioxidant and antibacterial activities of fruits of <italic>Eucalyptus globulus</italic> cultivated in Algeria</article-title>
<source>Ind Crops Prod</source>
<year iso-8601-date="2013">2013</year>
<volume>41</volume>
<fpage>85</fpage>
<lpage>9</lpage>
<pub-id pub-id-type="doi">10.1016/j.indcrop.2012.04.019</pub-id></element-citation>
</ref>
<ref id="B56">
<label>56</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Shiota</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Shimizu</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Sugiyama</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Morita</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Mizushima</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Tsuchiya</surname>
<given-names>T</given-names>
</name>
</person-group>
<article-title>Mechanisms of action of corilagin and tellimagrandin I that remarkably potentiate the activity of β-lactams against methicillin-resistant <italic>Staphylococcus aureus</italic></article-title>
<source>Microbiol Immunol</source>
<year iso-8601-date="2004">2004</year>
<volume>48</volume>
<fpage>67</fpage>
<lpage>73</lpage>
<pub-id pub-id-type="doi">10.1111/j.1348-0421.2004.tb03489.x</pub-id><pub-id pub-id-type="pmid">14734860</pub-id></element-citation>
</ref>
<ref id="B57">
<label>57</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Lim</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Strynadka</surname>
<given-names>NCJ</given-names>
</name>
</person-group>
<article-title>Structural basis for the β lactam resistance of PBP2a from methicillin-resistant <italic>Staphylococcus aureus</italic></article-title>
<source>Nat Struct Biol</source>
<year iso-8601-date="2002">2002</year>
<volume>9</volume>
<fpage>870</fpage>
<lpage>6</lpage>
<pub-id pub-id-type="doi">10.1038/nsb858</pub-id><pub-id pub-id-type="pmid">12389036</pub-id></element-citation>
</ref>
<ref id="B58">
<label>58</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Virtanen</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Puljula</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Walton</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Woodward</surname>
<given-names>MJ</given-names>
</name>
<name>
<surname>Karonen</surname>
<given-names>M</given-names>
</name>
</person-group>
<article-title>NMR metabolomics and DNA sequencing of <italic>Escherichia coli</italic> and <italic>Staphylococcus aureus</italic> cultures treated with hydrolyzable tannins</article-title>
<source>Metabolites</source>
<year iso-8601-date="2023">2023</year>
<volume>13</volume>
<elocation-id>320</elocation-id>
<pub-id pub-id-type="doi">10.3390/metabo13030320</pub-id><pub-id pub-id-type="pmid">36984760</pub-id><pub-id pub-id-type="pmcid">PMC10051465</pub-id></element-citation>
</ref>
<ref id="B59">
<label>59</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Álvarez-Martínez</surname>
<given-names>FJ</given-names>
</name>
<name>
<surname>Barrajón-Catalán</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Encinar</surname>
<given-names>JA</given-names>
</name>
<name>
<surname>Rodríguez-Díaz</surname>
<given-names>JC</given-names>
</name>
<name>
<surname>Micol</surname>
<given-names>V</given-names>
</name>
</person-group>
<article-title>Antimicrobial capacity of plant polyphenols against gram-positive bacteria: a comprehensive review</article-title>
<source>Curr Med Chem</source>
<year iso-8601-date="2020">2020</year>
<volume>27</volume>
<fpage>2576</fpage>
<lpage>606</lpage>
<pub-id pub-id-type="doi">10.2174/0929867325666181008115650</pub-id><pub-id pub-id-type="pmid">30295182</pub-id></element-citation>
</ref>
<ref id="B60">
<label>60</label>
<element-citation publication-type="confproc">
<person-group person-group-type="author">
<name>
<surname>Xiao</surname>
<given-names>SY</given-names>
</name>
<name>
<surname>Wen</surname>
<given-names>BQ</given-names>
</name>
<name>
<surname>Zhuang</surname>
<given-names>HY</given-names>
</name>
<name>
<surname>Wang</surname>
<given-names>JL</given-names>
</name>
<name>
<surname>Tang</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Chen</surname>
<given-names>HZ</given-names>
</name>
<etal>et al.</etal>
</person-group>
<comment>Extraction and antitumor activity of pedunculagin from eucalyptus leaves. International Conference on Biomedical Engineering and Biotechnology (iCBEB); 2012 May 28–30; Macau Macao. IEEE; 2012. pp. 280–2.</comment>
</element-citation>
</ref>
<ref id="B61">
<label>61</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Silva</surname>
<given-names>Fernandes A</given-names>
</name>
<name>
<surname>Hollanda</surname>
<given-names>Véras J</given-names>
</name>
<name>
<surname>Silva</surname>
<given-names>LS</given-names>
</name>
<name>
<surname>Puga</surname>
<given-names>SC</given-names>
</name>
<name>
<surname>Luiz</surname>
<given-names>Cardoso Bailão EF</given-names>
</name>
<name>
<surname>de Oliveira</surname>
<given-names>MG</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Pedunculagin isolated from <italic>Plinia cauliflora</italic> seeds exhibits genotoxic, antigenotoxic and cytotoxic effects in bacteria and human lymphocytes</article-title>
<source>J Toxicol Environ Health A</source>
<year iso-8601-date="2022">2022</year>
<volume>85</volume>
<fpage>353</fpage>
<lpage>63</lpage>
<pub-id pub-id-type="doi">10.1080/15287394.2021.2009947</pub-id><pub-id pub-id-type="pmid">34875975</pub-id></element-citation>
</ref>
<ref id="B62">
<label>62</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Zhao</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Bai</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Bu</surname>
<given-names>X</given-names>
</name>
<name>
<surname>Tang</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Han</surname>
<given-names>W</given-names>
</name>
<name>
<surname>Li</surname>
<given-names>D</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Microwave-assisted aqueous two-phase extraction of phenolic compounds from Ribes nigrum L. and its antibacterial effect on foodborne pathogens</article-title>
<source>Food Control</source>
<year iso-8601-date="2021">2021</year>
<volume>119</volume>
<elocation-id>107449</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.foodcont.2020.107449</pub-id></element-citation>
</ref>
<ref id="B63">
<label>63</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Al-Harbi</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Al-Wegaisi</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Moharram</surname>
<given-names>FA</given-names>
</name>
<name>
<surname>Shaaban</surname>
<given-names>M</given-names>
</name>
<name>
<surname>El-Rahman</surname>
<given-names>OA</given-names>
</name>
</person-group>
<article-title>Antibacterial and anti-hemolytic activity of tannins from Pimenta dioica against methicillin resistant Staphylococcus aureus</article-title>
<source>Bangladesh J Pharmacol</source>
<year iso-8601-date="2017">2017</year>
<volume>12</volume>
<fpage>63</fpage>
<lpage>8</lpage>
<pub-id pub-id-type="doi">10.3329/BJP.V12I1.29735</pub-id></element-citation>
</ref>
<ref id="B64">
<label>64</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Abdellaoui</surname>
<given-names>SE</given-names>
</name>
<name>
<surname>Destandau</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Krolikiewicz-Renimel</surname>
<given-names>I</given-names>
</name>
<name>
<surname>Cancellieri</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Toribio</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Jeronimo-Monteiro</surname>
<given-names>V</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Centrifugal partition chromatography for antibacterial bio-guided fractionation of <italic>Clidemia hirta</italic> roots</article-title>
<source>Sep Purif Technol</source>
<year iso-8601-date="2014">2014</year>
<volume>123</volume>
<fpage>221</fpage>
<lpage>8</lpage>
<pub-id pub-id-type="doi">10.1016/j.seppur.2013.12.036</pub-id></element-citation>
</ref>
<ref id="B65">
<label>65</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Orlova</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Kysil</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Tsvetkova</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Meshalkina</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Whaley</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Whaley</surname>
<given-names>AO</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Phytochemical characterization of water avens (<italic>Geum rivale</italic> L.) extracts: structure assignment and biological activity of the major phenolic constituents</article-title>
<source>Plants (Basel)</source>
<year iso-8601-date="2022">2022</year>
<volume>11</volume>
<elocation-id>2859</elocation-id>
<pub-id pub-id-type="doi">10.3390/plants11212859</pub-id><pub-id pub-id-type="pmid">36365312</pub-id><pub-id pub-id-type="pmcid">PMC9658556</pub-id></element-citation>
</ref>
<ref id="B66">
<label>66</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Zheng</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Shang</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Wu</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Wu</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Chen</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Wang</surname>
<given-names>Z</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Diclazuril inhibits biofilm formation and hemolysis of <italic>Staphylococcus aureus</italic></article-title>
<source>ACS Infect Dis</source>
<year iso-8601-date="2021">2021</year>
<volume>7</volume>
<fpage>1690</fpage>
<lpage>701</lpage>
<pub-id pub-id-type="doi">10.1021/acsinfecdis.1c00030</pub-id><pub-id pub-id-type="pmid">34019393</pub-id></element-citation>
</ref>
<ref id="B67">
<label>67</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Sanhueza</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Melo</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Montero</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Maisey</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Mendoza</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Wilkens</surname>
<given-names>M</given-names>
</name>
</person-group>
<article-title>Synergistic interactions between phenolic compounds identified in grape pomace extract with antibiotics of different classes against <italic>Staphylococcus aureus</italic> and <italic>Escherichia coli</italic></article-title>
<source>PLoS One</source>
<year iso-8601-date="2017">2017</year>
<volume>12</volume>
<elocation-id>e0172273</elocation-id>
<pub-id pub-id-type="doi">10.1371/journal.pone.0172273</pub-id><pub-id pub-id-type="pmid">28235054</pub-id><pub-id pub-id-type="pmcid">PMC5325233</pub-id></element-citation>
</ref>
<ref id="B68">
<label>68</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Pizzi</surname>
<given-names>A</given-names>
</name>
</person-group>
<article-title>Tannins medical/pharmacological and related applications: a critical review</article-title>
<source>Sustain Chem Pharm</source>
<year iso-8601-date="2021">2021</year>
<volume>22</volume>
<elocation-id>100481</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.scp.2021.100481</pub-id></element-citation>
</ref>
<ref id="B69">
<label>69</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Fidelis</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Araújo</surname>
<given-names>Vieira do Carmo M</given-names>
</name>
<name>
<surname>Azevedo</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Mendanha</surname>
<given-names>Cruz T</given-names>
</name>
<name>
<surname>Boscacci</surname>
<given-names>Marques M</given-names>
</name>
<name>
<surname>Myoda</surname>
<given-names>T</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Response surface optimization of phenolic compounds from jabuticaba (<italic>Myrciaria cauliflora</italic> [Mart.] O.Berg) seeds: antioxidant, antimicrobial, antihyperglycemic, antihypertensive and cytotoxic assessments</article-title>
<source>Food Chem Toxicol</source>
<year iso-8601-date="2020">2020</year>
<volume>142</volume>
<elocation-id>111439</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.fct.2020.111439</pub-id><pub-id pub-id-type="pmid">32450285</pub-id></element-citation>
</ref>
<ref id="B70">
<label>70</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Fidelis</surname>
<given-names>M</given-names>
</name>
<name>
<surname>do Carmo</surname>
<given-names>MAV</given-names>
</name>
<name>
<surname>da Cruz</surname>
<given-names>TM</given-names>
</name>
<name>
<surname>Azevedo</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Myoda</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Miranda</surname>
<given-names>Furtado M et al.</given-names>
</name>
</person-group>
<article-title>Camu-camu seed (<italic>Myrciaria dubia</italic>)—from side stream to an antioxidant, antihyperglycemic, antiproliferative, antimicrobial, antihemolytic, anti-inflammatory, and antihypertensive ingredient</article-title>
<source>Food Chem</source>
<year iso-8601-date="2020">2020</year>
<volume>310</volume>
<elocation-id>125909</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.foodchem.2019.125909</pub-id><pub-id pub-id-type="pmid">31816536</pub-id></element-citation>
</ref>
<ref id="B71">
<label>71</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Fujita</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Sarkar</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Wu</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Kennelly</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Shetty</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Genovese</surname>
<given-names>MI</given-names>
</name>
</person-group>
<article-title>Evaluation of phenolic-linked bioactives of camu-camu (<italic>Myrciaria dubia Mc. Vaugh</italic>) <italic>for antihyperglycemia, antihypertension, antimicrobial properties and cellular rejuvenation</italic></article-title>
<source>Food Res Int</source>
<year iso-8601-date="2015">2015</year>
<volume>77</volume>
<fpage>194</fpage>
<lpage>203</lpage>
<pub-id pub-id-type="doi">10.1016/J.FOODRES.2015.07.009</pub-id></element-citation>
</ref>
<ref id="B72">
<label>72</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Srećković</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Katanić</surname>
<given-names>Stanković JS</given-names>
</name>
<name>
<surname>Matić</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Mihailović</surname>
<given-names>NR</given-names>
</name>
<name>
<surname>Imbimbo</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Monti</surname>
<given-names>DM</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>
<italic>Lythrum salicaria</italic> L. (Lythraceae) as a promising source of phenolic compounds in the modulation of oxidative stress: comparison between aerial parts and root extracts</article-title>
<source>Ind Crops Prod</source>
<year iso-8601-date="2020">2020</year>
<volume>155</volume>
<elocation-id>112781</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.indcrop.2020.112781</pub-id></element-citation>
</ref>
<ref id="B73">
<label>73</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Nohynek</surname>
<given-names>LJ</given-names>
</name>
<name>
<surname>Alakomi</surname>
<given-names>HL</given-names>
</name>
<name>
<surname>Kähkönen</surname>
<given-names>MP</given-names>
</name>
<name>
<surname>Heinonen</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Helander</surname>
<given-names>IM</given-names>
</name>
<name>
<surname>Oksman-Caldentey</surname>
<given-names>KM</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Berry phenolics: antimicrobial properties and mechanisms of action against severe human pathogens</article-title>
<source>Nutr Cancer</source>
<year iso-8601-date="2006">2006</year>
<volume>54</volume>
<fpage>18</fpage>
<lpage>32</lpage>
<pub-id pub-id-type="doi">10.1207/s15327914nc5401_4</pub-id><pub-id pub-id-type="pmid">16800770</pub-id></element-citation>
</ref>
<ref id="B74">
<label>74</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Przybylska</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Kucharska</surname>
<given-names>AZ</given-names>
</name>
<name>
<surname>Cybulska</surname>
<given-names>I</given-names>
</name>
<name>
<surname>Sozański</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Piórecki</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Fecka</surname>
<given-names>I</given-names>
</name>
</person-group>
<article-title>
<italic>Cornus mas L. Stones</italic>: a valuable by-product as an ellagitannin source with high antioxidant potential</article-title>
<source>Molecules</source>
<year iso-8601-date="2020">2020</year>
<volume>25</volume>
<elocation-id>4646</elocation-id>
<pub-id pub-id-type="doi">10.3390/molecules25204646</pub-id><pub-id pub-id-type="pmid">33053845</pub-id><pub-id pub-id-type="pmcid">PMC7587210</pub-id></element-citation>
</ref>
<ref id="B75">
<label>75</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Moilanen</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Karonen</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Tähtinen</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Jacquet</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Quideau</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Salminen</surname>
<given-names>JP</given-names>
</name>
</person-group>
<article-title>Biological activity of ellagitannins: effects as anti-oxidants, pro-oxidants and metal chelators</article-title>
<source>Phytochemistry</source>
<year iso-8601-date="2016">2016</year>
<volume>125</volume>
<fpage>65</fpage>
<lpage>72</lpage>
<pub-id pub-id-type="doi">10.1016/j.phytochem.2016.02.008</pub-id><pub-id pub-id-type="pmid">26899362</pub-id></element-citation>
</ref>
<ref id="B76">
<label>76</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Boulekbache-Makhlouf</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Meudec</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Mazauric</surname>
<given-names>JP</given-names>
</name>
<name>
<surname>Madani</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Cheynier</surname>
<given-names>V</given-names>
</name>
</person-group>
<article-title>Qualitative and semi-quantitative analysis of phenolics in <italic>Eucalyptus globulus</italic> leaves by high-performance liquid chromatography coupled with diode array detection and electrospray ionisation mass spectrometry</article-title>
<source>Phytochem Anal</source>
<year iso-8601-date="2013">2013</year>
<volume>24</volume>
<fpage>162</fpage>
<lpage>70</lpage>
<pub-id pub-id-type="doi">10.1002/pca.2396</pub-id><pub-id pub-id-type="pmid">22930658</pub-id></element-citation>
</ref>
<ref id="B77">
<label>77</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>de Lima Paula</surname>
<given-names>P</given-names>
</name>
<name>
<surname>de Oliveira Lemos</surname>
<given-names>AS</given-names>
</name>
<name>
<surname>Campos</surname>
<given-names>LM</given-names>
</name>
<name>
<surname>Ferreira</surname>
<given-names>TG</given-names>
</name>
<name>
<surname>Freitas</surname>
<given-names>de Souza T</given-names>
</name>
<name>
<surname>Queiroz</surname>
<given-names>LS</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Pharmacological investigation of antioxidant and anti-inflammatory activities of leaves and branches extracts from <italic>Plinia cauliflora</italic> (Jaboticaba)</article-title>
<source>J Ethnopharmacol</source>
<year iso-8601-date="2021">2021</year>
<volume>280</volume>
<elocation-id>114463</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.jep.2021.114463</pub-id><pub-id pub-id-type="pmid">34352328</pub-id></element-citation>
</ref>
<ref id="B78">
<label>78</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Moon</surname>
<given-names>JH</given-names>
</name>
<name>
<surname>Kim</surname>
<given-names>JM</given-names>
</name>
<name>
<surname>Lee</surname>
<given-names>U</given-names>
</name>
<name>
<surname>Kang</surname>
<given-names>JY</given-names>
</name>
<name>
<surname>Kim</surname>
<given-names>MJ</given-names>
</name>
<name>
<surname>Lee</surname>
<given-names>HL</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Walnut prevents cognitive impairment by regulating the synaptic and mitochondrial dysfunction via JNK signaling and apoptosis pathway in high-fat diet-induced C57BL/6 mice</article-title>
<source>Molecules</source>
<year iso-8601-date="2022">2022</year>
<volume>27</volume>
<elocation-id>5316</elocation-id>
<pub-id pub-id-type="doi">10.3390/molecules27165316</pub-id><pub-id pub-id-type="pmid">36014555</pub-id><pub-id pub-id-type="pmcid">PMC9414791</pub-id></element-citation>
</ref>
<ref id="B79">
<label>79</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Chen</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Wang</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Ou</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Chen</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Xiao</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Liu</surname>
<given-names>G</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Cellular antioxidant activities of polyphenols isolated from Eucalyptus leaves (<italic>Eucalyptus grandis</italic> × <italic>Eucalyptus urophylla</italic> GL9)</article-title>
<source>J Funct Foods</source>
<year iso-8601-date="2014">2014</year>
<volume>7</volume>
<fpage>737</fpage>
<lpage>45</lpage>
<pub-id pub-id-type="doi">10.1016/j.jff.2013.12.003</pub-id></element-citation>
</ref>
<ref id="B80">
<label>80</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>de Oliveira Schmidt</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Rockett</surname>
<given-names>FC</given-names>
</name>
<name>
<surname>André</surname>
<given-names>Vinícus Bazzan K</given-names>
</name>
<name>
<surname>Schmidt</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Rodrigues</surname>
<given-names>E</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>New insights into the phenolic compounds and antioxidant capacity of feijoa and cherry fruits cultivated in Brazil</article-title>
<source>Food Res Int</source>
<year iso-8601-date="2020">2020</year>
<volume>136</volume>
<elocation-id>109564</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.foodres.2020.109564</pub-id><pub-id pub-id-type="pmid">32846605</pub-id></element-citation>
</ref>
<ref id="B81">
<label>81</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Kim</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Yin</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Hwang</surname>
<given-names>IH</given-names>
</name>
<name>
<surname>Park</surname>
<given-names>DH</given-names>
</name>
<name>
<surname>Lee</surname>
<given-names>EK</given-names>
</name>
<name>
<surname>Kim</surname>
<given-names>MJ</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Anti-acne vulgaris effects of pedunculagin from the leaves of<italic> Quercus mongolica</italic> by anti-inflammatory activity and 5α-reductase inhibition</article-title>
<source>Molecules</source>
<year iso-8601-date="2020">2020</year>
<volume>25</volume>
<elocation-id>2154</elocation-id>
<pub-id pub-id-type="doi">10.3390/molecules25092154</pub-id><pub-id pub-id-type="pmid">32380665</pub-id><pub-id pub-id-type="pmcid">PMC7249114</pub-id></element-citation>
</ref>
<ref id="B82">
<label>82</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>de Andrade Neves</surname>
<given-names>N</given-names>
</name>
<name>
<surname>César</surname>
<given-names>Stringheta P</given-names>
</name>
<name>
<surname>Ferreira</surname>
<given-names>da Silva I</given-names>
</name>
<name>
<surname>García-Romero</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Gómez-Alonso</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Hermosín-Gutiérrez</surname>
<given-names>I</given-names>
</name>
</person-group>
<article-title>Identification and quantification of phenolic composition from different species of Jabuticaba (<italic>Plinia</italic> spp.) by HPLC-DAD-ESI/MS<sup>n</sup></article-title>
<source>Food Chem</source>
<year iso-8601-date="2021">2021</year>
<volume>355</volume>
<elocation-id>129605</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.foodchem.2021.129605</pub-id><pub-id pub-id-type="pmid">33799238</pub-id></element-citation>
</ref>
<ref id="B83">
<label>83</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Li</surname>
<given-names>W</given-names>
</name>
<name>
<surname>Zhang</surname>
<given-names>X</given-names>
</name>
<name>
<surname>He</surname>
<given-names>Z</given-names>
</name>
<name>
<surname>Chen</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Li</surname>
<given-names>Z</given-names>
</name>
<name>
<surname>Meng</surname>
<given-names>T</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>
<italic>In vitro</italic> and <italic>in vivo</italic> antioxidant activity of eucalyptus leaf polyphenols extract and its effect on chicken meat quality and cecum microbiota</article-title>
<source>Food Res Int</source>
<year iso-8601-date="2020">2020</year>
<volume>136</volume>
<elocation-id>109302</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.foodres.2020.109302</pub-id><pub-id pub-id-type="pmid">32846514</pub-id></element-citation>
</ref>
<ref id="B84">
<label>84</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Almeida</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Murta</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Nunes</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Baby</surname>
<given-names>AR</given-names>
</name>
<name>
<surname>Fernandes</surname>
<given-names>Â</given-names>
</name>
<name>
<surname>Barros</surname>
<given-names>L</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Characterization of lipid extracts from the <italic>Hermetia illucens</italic> larvae and their bioactivities for potential use as pharmaceutical and cosmetic ingredients</article-title>
<source>Heliyon</source>
<year iso-8601-date="2022">2022</year>
<volume>8</volume>
<elocation-id>e09455</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.heliyon.2022.e09455</pub-id><pub-id pub-id-type="pmid">35637671</pub-id><pub-id pub-id-type="pmcid">PMC9142853</pub-id></element-citation>
</ref>
<ref id="B85">
<label>85</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Vega</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Bonomi-Barufi</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Gómez-Pinchetti</surname>
<given-names>JL</given-names>
</name>
<name>
<surname>Figueroa</surname>
<given-names>FL</given-names>
</name>
</person-group>
<article-title>Cyanobacteria and red macroalgae as potential sources of antioxidants and UV radiation-absorbing compounds for cosmeceutical applications</article-title>
<source>Mar Drugs</source>
<year iso-8601-date="2020">2020</year>
<volume>18</volume>
<elocation-id>659</elocation-id>
<pub-id pub-id-type="doi">10.3390/md18120659</pub-id><pub-id pub-id-type="pmid">33371308</pub-id><pub-id pub-id-type="pmcid">PMC7767163</pub-id></element-citation>
</ref>
<ref id="B86">
<label>86</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Aires</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Carvalho</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Saavedra</surname>
<given-names>MJ</given-names>
</name>
</person-group>
<article-title>Valorization of solid wastes from chestnut industry processing: extraction and optimization of polyphenols, tannins and ellagitannins and its potential for adhesives, cosmetic and pharmaceutical industry</article-title>
<source>Waste Manag</source>
<year iso-8601-date="2016">2016</year>
<volume>48</volume>
<fpage>457</fpage>
<lpage>64</lpage>
<pub-id pub-id-type="doi">10.1016/j.wasman.2015.11.019</pub-id><pub-id pub-id-type="pmid">26626811</pub-id></element-citation>
</ref>
<ref id="B87">
<label>87</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Okumus</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Bakkalbas</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Javidipour</surname>
<given-names>I</given-names>
</name>
<name>
<surname>Raciye</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Ceylan</surname>
<given-names>Z</given-names>
</name>
</person-group>
<article-title>A novel coating material: ellagitannins-loaded maltodextrin and lecithin-based nanomaterials</article-title>
<source>Food Biosci</source>
<year iso-8601-date="2021">2021</year>
<volume>42</volume>
<elocation-id>101158</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.fbio.2021.101158</pub-id></element-citation>
</ref>
<ref id="B88">
<label>88</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Torgbo</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Rugthaworn</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Sukatta</surname>
<given-names>U</given-names>
</name>
<name>
<surname>Sukyai</surname>
<given-names>P</given-names>
</name>
</person-group>
<article-title>Biological characterization and quantification of rambutan (<italic>Nephelium lappaceum</italic> L.) peel extract as a potential source of valuable minerals and ellagitannins for industrial applications</article-title>
<source>ACS Omega</source>
<year iso-8601-date="2022">2022</year>
<volume>7</volume>
<fpage>34647</fpage>
<lpage>56</lpage>
<pub-id pub-id-type="doi">10.1021/acsomega.2c04646</pub-id><pub-id pub-id-type="pmid">36188307</pub-id><pub-id pub-id-type="pmcid">PMC9521024</pub-id></element-citation>
</ref>
<ref id="B89">
<label>89</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Li</surname>
<given-names>Z</given-names>
</name>
<name>
<surname>Summanen</surname>
<given-names>PH</given-names>
</name>
<name>
<surname>Komoriya</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Henning</surname>
<given-names>SM</given-names>
</name>
<name>
<surname>Lee</surname>
<given-names>RP</given-names>
</name>
<name>
<surname>Carlson</surname>
<given-names>E</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Pomegranate ellagitannins stimulate growth of gut bacteria <italic>in vitro</italic>: implications for prebiotic and metabolic effects</article-title>
<source>Anaerobe</source>
<year iso-8601-date="2015">2015</year>
<volume>34</volume>
<fpage>164</fpage>
<lpage>8</lpage>
<pub-id pub-id-type="doi">10.1016/j.anaerobe.2015.05.012</pub-id><pub-id pub-id-type="pmid">26051169</pub-id></element-citation>
</ref>
<ref id="B90">
<label>90</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Fan</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Fusco</surname>
<given-names>JL</given-names>
</name>
<name>
<surname>Rosenberg</surname>
<given-names>DW</given-names>
</name>
</person-group>
<article-title>Antioxidant and Anti-inflammatory properties of walnut constituents: focus on personalized cancer prevention and the microbiome</article-title>
<source>Antioxidants (Basel)</source>
<year iso-8601-date="2023">2023</year>
<volume>12</volume>
<elocation-id>982</elocation-id>
<pub-id pub-id-type="doi">10.3390/antiox12050982</pub-id><pub-id pub-id-type="pmid">37237848</pub-id><pub-id pub-id-type="pmcid">PMC10215340</pub-id></element-citation>
</ref>
<ref id="B91">
<label>91</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Cegiełka</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Hać-Szymańczuk</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Piwowarek</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Dasiewicz</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Słowiński</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Wrońska</surname>
<given-names>K</given-names>
</name>
</person-group>
<article-title>The use of bioactive properties of sage preparations to improve the storage stability of low-pressure mechanically separated meat from chickens2</article-title>
<source>Poult Sci</source>
<year iso-8601-date="2019">2019</year>
<volume>98</volume>
<fpage>5045</fpage>
<lpage>53</lpage>
<pub-id pub-id-type="doi">10.3382/ps/pez242</pub-id><pub-id pub-id-type="pmid">31065702</pub-id></element-citation>
</ref>
<ref id="B92">
<label>92</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Firuzi</surname>
<given-names>MR</given-names>
</name>
<name>
<surname>Niakousari</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Eskandari</surname>
<given-names>MH</given-names>
</name>
<name>
<surname>Keramat</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Gahruie</surname>
<given-names>HH</given-names>
</name>
<name>
<surname>Mousavi</surname>
<given-names>Khaneghah A</given-names>
</name>
</person-group>
<article-title>Incorporation of pomegranate juice concentrate and pomegranate rind powder extract to improve the oxidative stability of frankfurter during refrigerated storage</article-title>
<source>LWT</source>
<year iso-8601-date="2019">2019</year>
<volume>102</volume>
<fpage>237</fpage>
<lpage>45</lpage>
<pub-id pub-id-type="doi">10.1016/j.lwt.2018.12.048</pub-id></element-citation>
</ref>
<ref id="B93">
<label>93</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Mantzourani</surname>
<given-names>I</given-names>
</name>
<name>
<surname>Daoutidou</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Dasenaki</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Nikolaou</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Alexopoulos</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Terpou</surname>
<given-names>A</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Plant extract and essential oil application against food-borne pathogens in raw pork meat</article-title>
<source>Foods</source>
<year iso-8601-date="2022">2022</year>
<volume>11</volume>
<elocation-id>861</elocation-id>
<pub-id pub-id-type="doi">10.3390/foods11060861</pub-id><pub-id pub-id-type="pmid">35327283</pub-id><pub-id pub-id-type="pmcid">PMC8955163</pub-id></element-citation>
</ref>
<ref id="B94">
<label>94</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Stojanović-Radić</surname>
<given-names>Z</given-names>
</name>
<name>
<surname>Pejčić</surname>
<given-names>MG</given-names>
</name>
<name>
<surname>Joković</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Jokanović</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Ivić</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Šojić</surname>
<given-names>B</given-names>
</name>
<etal>et al.</etal>
</person-group>
<article-title>Inhibition of <italic>Salmonella</italic> enteritidis growth and storage stability in chicken meat treated with basil and rosemary essential oils alone or in combination</article-title>
<source>Food Control</source>
<year iso-8601-date="2018">2018</year>
<volume>90</volume>
<fpage>332</fpage>
<lpage>43</lpage>
<pub-id pub-id-type="doi">10.1016/J.FOODCONT.2018.03.013</pub-id></element-citation>
</ref>
<ref id="B95">
<label>95</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Moghadam</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Salami</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Mohammadian</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Khodadadi</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Emam-Djomeh</surname>
<given-names>Z</given-names>
</name>
</person-group>
<article-title>Development of antioxidant edible films based on mung bean protein enriched with pomegranate peel</article-title>
<source>Food Hydrocoll</source>
<year iso-8601-date="2020">2020</year>
<volume>104</volume>
<elocation-id>105735</elocation-id>
<pub-id pub-id-type="doi">10.1016/j.foodhyd.2020.105735</pub-id></element-citation>
</ref>
</ref-list>
</back>
</article>