Medicinal plants for skin and wound-healing in Brazil: an ethnobotanical and antibacterial review
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Medicinal plants for skin and wound-healing in Brazil: an ethnobotanical and antibacterial review

Affiliation:

Oswaldo Cruz Foundation, Fiocruz, René Rachou Institute, Fiocruz Minas, Bioactive Natural Products Chemistry Group, Belo Horizonte 30190-002, Brazil

Email: betania.cota@fiocruz.br

ORCID: https://orcid.org/0000-0002-0041-2043

Betania Barros Cota
*

Explor Drug Sci. 2026;4:1008164 DOI: https://doi.org/10.37349/eds.2026.1008164

Received: January 16, 2026 Accepted: April 12, 2026 Published: June 17, 2026

Academic Editor: Mozaniel Santana de Oliveira, Federal University of Pará, Brazil

The article belongs to the special issue Discovery and development of new antibacterial compounds

Abstract

Brazil harbors remarkable biological and cultural diversity, reflected in a rich body of traditional knowledge regarding the medicinal use of plants. This study synthesized ethnobotanical evidence on plants traditionally used for skin and wound healing in Brazil and examined their convergence with available antibacterial data. An integrative literature review identified twenty ethnobotanical studies, mainly involving rural populations and local residents, reporting 51 plant species traditionally used for skin and wound healing across 22 genera, predominantly native and mainly documented in the Northeastern and Northern regions. The most frequently cited species included Aloe vera (L.) Burm.f. and Anacardium occidentale L., followed by Stryphnodendron adstringens (Mart.) Coville. Fabaceae and Anacardiaceae concentrated the highest number of species with confirmed antibacterial activity, followed by Piperaceae and Euphorbiaceae, which also showed a high proportional representation of active species. A meaningful convergence between ethnobotanical use and experimental antibacterial evidence was observed for more than half of the plants, frequently against Staphylococcus aureus, a key pathogen in wound infections. Antibacterial data were predominantly derived from in vitro assays using non-standardized extracts, and only a limited number of studies reported possible mechanisms of action, such as membrane disruption and biofilm inhibition. Furthermore, few investigations evaluated antibacterial activity in infected wound models or quantified bacterial load reduction in vivo. Future studies should prioritize chemically standardized extracts, testing against resistant clinical strains and mature biofilm models, and validation of safety and therapeutic efficacy in clinical investigations. These findings reveal a gap between traditional use and clinically validated applications, underscoring the urgent need for standardized research approaches and reinforcing Brazil’s potential as a strategic reservoir of bioactive plant resources for primary health care. Addressing these limitations is essential to strengthening the translational basis for the rational use of medicinal plants in primary health care and public health contexts.

Keywords

ethnobotanical knowledge, medicinal plant, wound healing, cutaneous infections, burn injuries, antibacterial activity, minimum inhibitory concentration, integrative review

Introduction

Brazil, a country of remarkable biological and cultural diversity, is home to multiple biomes such as the Amazon, Atlantic Forest, Cerrado, Caatinga, and Pantanal, as well as a rich flora with significant therapeutic potential. This biodiversity, combined with a historical formation marked by the presence of Indigenous, African, and European peoples, has resulted in a wide repertoire of traditional knowledge related to the medicinal use of plants. Across different regions of the country, ethnobotanical studies have documented the knowledge of traditional communities, including Quilombola, Indigenous, riverside, and “raizeiros” (traditional Brazilian herbal healers) populations, on plant species used in healthcare practices [1, 2].

The use of medicinal plants in these contexts is often associated with the remote location of these populations and their limited access to healthcare services and industrialized medicines. Furthermore, economic factors and the appreciation of culturally inherited practices contribute to the preservation and transmission of this knowledge [3]. Among the various therapeutic purposes, the traditional application of plant species for the treatment of burns, wounds, and bacterial skin infections stands out as a common practice in the daily lives of these communities, frequently managed with the use of natural resources available in the local environment. Because infection is a major factor that can delay or impair wound healing, the investigation of the antibacterial properties of these traditionally used species becomes particularly relevant.

After an injury, bacterial invasion is frequent, either through migration of the skin microbiota to deeper tissues or exposure to external microorganisms, potentially resulting in infection. Biofilm formation on the wound bed protects bacteria, promotes their proliferation, and increases their tolerance to antibacterial treatments, contributing to lesion persistence and delayed healing, particularly in the context of rising antimicrobial resistance [4].

Even mild wounds and burns can serve as entry points for pathogenic microorganisms and increase the risk of secondary infections. Colonization by Staphylococcus aureus (S. aureus), including methicillin-resistant strains, is associated with increased lesion severity and a higher risk of local and systemic complications. A study conducted in primary healthcare units of the Brazilian Unified Health System found a prevalence of 51.5% for S. aureus and 8.7% for methicillin-resistant S. aureus among patients with infected wounds [5], highlighting the relevance of these infections even outside the hospital setting.

Wounds and burns are considered an important public health concern due to their frequency, possible complications, and socioeconomic impact [6, 7]. Chronic wounds, such as pressure injuries, diabetic foot ulcers, and venous or arterial ulcers, result from disordered healing mechanisms and represent a significant burden on healthcare systems [8, 9]. Burns represent an important cause of morbidity and mortality in Brazil, particularly among vulnerable populations such as children and older adults [6, 9].

The management of skin lesions imposes a significant economic burden and affects patients’ quality of life. Aging, chronic diseases, biofilm formation, and microbial resistance contribute to lesion persistence and increased treatment costs [4, 7, 10].

Although severe infections such as sepsis [9, 11] may occur as a consequence of burns or poorly managed or infected skin lesions, most of these conditions are less severe and are managed outside the hospital setting, within the community, generally involving limited clinical manifestations [12]. In such situations, the use of medicinal plants represents a widely used, accessible, and culturally rooted therapeutic alternative, especially in resource-limited contexts. In addition to their traditional role, several medicinal plants and their secondary metabolites have demonstrated proven antibacterial activity, including against strains resistant to antimicrobials used in clinical practice, with many of their mechanisms of action already characterized [13]. Therefore, integrating ethnobotanical data with experimental antibacterial evidence is essential to critically assess the therapeutic plausibility of these species, validate their traditional use, and identify priority candidates for further pharmacological investigation and potential public health applications.

Although a previous review has addressed the use of medicinal plants for wound healing in Brazil, its scope was limited to the southern region of the country [14]. This review is particularly relevant as it bridges traditional ethnobotanical knowledge with pharmacological evidence, providing a critical synthesis of medicinal plants most frequently reported in Brazilian communities for the treatment of skin conditions with potential bacterial etiology. By systematizing data on antibacterial activity obtained from standardized assays, such as minimum inhibitory concentration (MIC) determinations, this study not only highlights the diversity of traditionally used species but also identifies a restricted group of taxa consistently cited across studies. These taxa represent priority candidates for subsequent investigations aimed at elucidating antibacterial mechanisms of action or exploring their relevance in the context of antimicrobial resistance.

Materials and Methods

This integrative review followed methodological elements adapted from the Joanna Briggs Institute [15].

To be included in the study, publications had to meet the following criteria: (i) ethnobotanical surveys conducted in Brazilian communities; (ii) reports of plants explicitly indicated for the treatment of wounds, burns or skin problems, with scientific names provided for each species; (iii) articles written in Portuguese or English and published within the last ten years; and (iv) peer-reviewed original research articles. Reviews, book chapters, books, theses, dissertations, monographs, letters to the editor, and case reports were excluded.

The literature search was conducted in three electronic databases: the Virtual Health Library (VHL/BVS), Science Direct, and Scopus. Database searches were updated up to June 2025. The search strategy was adapted to the syntax of each database, using controlled descriptors and free-text keywords combined with Boolean operators (‘OR’ and ‘AND’).

1: Virtual Health Library (VHL/BVS): (“levantamento etnobotânico” OR “estudo etnobotânico” OR “uso tradicional” OR “plantas medicinais”) AND (feridas OR cicatrização OR úlcera* OR erisipela OR “doenças de pele” OR pele).

2: Science Direct: (wound OR wound healing) AND (ethnobotany OR ethnobotanical survey) AND Brazil.

3: Scopus: TITLE-ABS (“ethnobotanical survey” OR “ethnobotanical study” OR “traditional use” OR “medicinal plants”) AND TITLE-ABS (wounds OR healing OR ulcer* OR erysipelas OR “skin diseases” OR dermatological) AND (LIMIT-TO (AFFILCOUNTRY, “Brazil”)) AND (LIMIT-TO (DOCTYPE, “ar”) OR LIMIT-TO (LANGUAGE, “English”) OR LIMIT-TO (LANGUAGE, “Portuguese”)).

Initially, titles and abstracts were evaluated and selected according to the inclusion and exclusion criteria. The papers were retrieved, and after reading, they were evaluated again according to the same criteria.

The Population–Concept–Context (PCC) strategy was applied, where the population refers to Brazilian communities, the concept to medicinal plants, and the context to wounds and skin conditions related to antibacterial use.

This review was designed as a narrative and critical synthesis of the literature addressing two main questions: (i) which medicinal plants are most frequently reported in Brazilian ethnobotanical surveys for the treatment of wounds and skin conditions; and (ii) which of these plants have demonstrated antibacterial activity in scientific studies and which remain unexplored.

The extracted information included the scientific names of plants associated with skin-related indications such as wounds, wound healing, cicatrization, burns, abscesses, furuncles, erysipelas, and skin infections or disorders potentially linked to antibacterial activity. The results were organized according to database source, study location, and region in Brazil, study population, and author with year of publication.

Plant genera represented by more than three species citations across the ethnobotanical studies were then identified, regardless of whether these citations occurred within a single study or across multiple studies, excluding generic records (sp., spp., cf.). The scientific names and plant origins (native or exotic) were verified using the Tropicos (https://www.tropicos.org/) and Reflora (https://reflora.jbrj.gov.br) databases. When synonymous names were identified across studies, records were grouped and harmonized under the currently accepted name to ensure taxonomic consistency.

Additional searches were conducted in SciFinder®, complemented by Google Scholar and the CAPES Journals Portal, using the scientific name of each species in combination with two sets of terms: (i) antibacterial activity (e.g., antibacterial, antimicrobial, MIC) and (ii) wound-healing–related uses (e.g., wound healing, burns, skin). This step aimed to identify representative pharmacological studies related to the reported ethnobotanical uses.

For antibacterial activity, the main focus of this review, only studies reporting MIC values were included, since these values provide a more standardized and comparable measure of antibacterial activity across studies. Although MIC values below 100 µg/mL are often considered indicative of strong activity for crude extracts [16], no universally accepted threshold exists for plant-derived products. Therefore, an inclusive cutoff of ≤ 350 µg/mL was predefined and applied consistently across studies, reflecting the aim of prioritizing species supported by both traditional use and measurable antibacterial activity rather than identifying immediate drug leads.

Studies evaluating wound-healing activity using nanoparticle-based formulations derived from plant extracts, as well as in vitro wound-healing assays (e.g., cell migration or scratch assays), were excluded, as these approaches rely on mechanistic pathways distinct from those of crude plant extracts.

Main findings about ethnobotanical studies

A total of 620 studies were initially identified, and twenty ethnobotanical studies were included in this survey, retrieved from BVS (n = 5), Scopus (n = 6), and ScienceDirect (n = 9) (Table 1, Figure 1). Although the search was updated until June 2025, most of the included studies were published in 2015 and 2016. These studies were predominantly conducted in the Northeastern and Northern regions of Brazil, particularly in the states of Bahia and Ceará. The study populations were mainly composed of local residents, predominantly from rural communities [1, 3, 1734].

 Synthesis of selected ethnopharmacological studies reporting medicinal plants for antibacterial-related skin conditions in Brazil.

IDSourceStudy location (Brazil)Brazil regionStudy population*Author(s)
1BVSMato Grosso do SulCentral-WesternLocal residents[1]
2Science DirectCearáNortheasternLocal specialists[17]
3ScopusBahiaNortheasternSpecific cultural/professional groups[18]
4ScopusCearáNortheasternLocal specialists[19]
5Science DirectSão PauloSoutheasternLocal residents[20]
6ScopusCeará and PernambucoNortheasternLocal specialists[21]
7Science DirectMato GrossoCentral-WesternSpecific cultural/professional groups[22]
8ScopusMinas GeraisSoutheasternLocal residents[23]
9Science DirectCearáNortheasternLocal residents[24]
10ScopusRio Grande do SulSouthernLocal residents[25]
11BVSAlagoasNortheasternHerbal vendors from street markets[26]
12ScopusRoraima and AmazonasNorthernLocal residents[27]
13Science DirectBahiaNortheasternLocal residents[28]
14BVSParaíbaNortheasternHerbal vendors from street markets[3]
15Science DirectParanáSouthernLocal residents[29]
16Science DirectMato GrossoCentral-WesternLocal residents[30]
17BVSRio Grande do SulSouthernLocal residents[31]
18Science DirectPernambucoNortheasternLocal residents[32]
19Science DirectSanta CatarinaSouthernLocal residents[33]
20BVSMaranhãoNortheasternLocal specialists[34]

* Local residents (including local population, residents, and rural communities). Local specialists (including informants or local experts, and rural informants). Herbal vendors from street markets (including both terms referring to “raizeiros”). Specific cultural/professional groups (including Quilombola community, families of farmers, riverine experts, and traditional healers).

An ethnobotanical evidence schematic summarizing the selection of medicinal plants used for skin conditions in Brazil. A total of 620 records were identified through database searches in BVS, Scopus, and ScienceDirect, from which 20 ethnobotanical studies were included. These studies reported 333 records of plant species related to skin conditions. After applying the selection criterion of the most frequently cited genera (n ≥ 3), 51 species distributed across 22 genera were retained for analysis. Most species were native to Brazil (n = 41), while 10 were exotic. Ethnobotanical uses were grouped into four categories associated with skin conditions of potential bacterial relevance.

In total, 333 mentions of plant species (data not shown) were reported in ethnobotanical studies addressing skin conditions of potential bacterial etiology, including repeated citations of the same species across different ethnobotanical studies for skin-related treatments. After applying the selection criterion of the most frequently cited genera (n ≥ 3), 51 valid species were identified (Supplementary material), distributed across 22 genera and 15 families, of which 41 were native, and 10 were exotics. These results indicate that ethnobotanical knowledge, although diverse, tends to be concentrated in a smaller subset of taxa, many of which are part of the Brazilian flora with recognized medicinal importance.

The most frequently cited species (Supplementary material) were Aloe vera (L.) Burm.f. and Anacardium occidentale L. (A. occidentale L., 8 reports each), followed by Symphytum officinale L. and Stryphnodendron adstringens (Mart.) Coville (7 reports each), Myracrodruon urundeuva Allemão (6 reports), Alternanthera brasiliana (L.) Kuntze and Dysphania ambrosioides (L.) Mosyakin & Clemants (5 reports each), and Ximenia americana L., Psidium guajava L., and Calendula officinalis L. (4 reports each). This pattern shows that in some cases, such as Symphytum and Stryphnodendron, citations were strongly concentrated in a single species, while in others, such as Alternanthera, Croton, Piper, and Sida, references were spread across different species, indicating that their cultural importance is recognized more at the genus level than in a single dominant taxon.

The ethnobotanical indications reported for the 51 selected species were grouped into four main categories. Although the search strategy retrieved a broad range of skin-related uses, the present analysis focused on conditions of potential bacterial relevance. Most species were associated with wounds and healing (37 species). Smaller proportions referred to skin conditions and cleansing (17 species), infections and abscesses such as furuncles and erysipelas (14 species), burns (6 species), and bruises (1 species), with some species reported for more than one indication.

Most surveys were conducted in Northeastern and Northern Brazil, where native species such as M. urundeuva and S. adstringens were frequently reported. In contrast, exotic and widely cultivated species like A. vera and Symphytum officinale were more common in studies from other regions, such as the Southeastern and Southern regions. These findings reflect the geographic distribution of the surveys rather than nationwide patterns of use.

Correspondences between traditional uses and experimental evidence of wound-healing and antibacterial activities

This section explores the alignment between ethnobotanical indications for skin wounds and skin disorders and experimental evidence of wound-healing and antibacterial activities. Traditional uses and regional occurrence of the selected plant species are first presented, followed by in vivo wound-healing studies and in vitro antibacterial evaluations using broth microdilution assays, considering MIC values ≤ 350 µg/mL. Additional data and extended analyses are available in the Supplementary material.

Alternanthera genus

The three Alternanthera species cited in the selected reports, Alternanthera brasiliana (L.) Kuntze (“Benzetacil”), A. dentata (Moench) Stuchlík ex R.E. Fr. (“penicilina”), and A. ramosissima (Mart.) Chodat (“ampicilina”) are native species reported for the treatment of skin conditions, mainly using their leaves [18, 22, 2831]. An experimental study in Wistar rats supports the wound-healing potential of A. brasiliana, as the topical application of a 20% hydroalcoholic leaf extract incorporated into a 2% carbopol gel significantly accelerated re-epithelialization and collagen deposition when compared to vehicle control. Despite this healing activity, the same extract exhibited a relatively high MIC value (2,000 µg/mL) against S. aureus [35]. Similar healing effects were reported with a 5% (w/w) ointment containing the methanolic leaf extract [36]. Regarding antibacterial activity, the most significant effect was observed against Mycobacterium smegmatis, with an MIC of 15.6 µg/mL [37].

Dysphania genus

Dysphania ambrosioides (L.) Mosyakin & Clemants (Chenopodium ambrosioides syn.) is native to Central and South America. All parts of this plant, popularly known in Brazil as “erva-de-santa-maria” or “mastruz”, are traditionally used to treat skin conditions such as burns and bruises, as well as for wound healing, in the Central-Western, Northeastern, and Southeastern regions [1, 18, 20, 22, 28]. In rat excisional wound models, topical application of C. ambrosioides extracts accelerated wound contraction and tissue repair. Ethanolic extracts (1–5%) reduced lesion area at later healing stages [38], while an aqueous leaf extract promoted faster early wound contraction and improved granulation tissue organization and partial re-epithelialization [39], supporting the traditional use of this species in skin wound care.

Beyond its direct effects on tissue repair, antibacterial activity may contribute to the healing process by reducing microbial burden at the wound site. In this context, the hydroethanolic leaf extract inhibits Helicobacter pylori (MIC 200 µg/mL) [40], while the essential oil from aerial parts exhibits broad-spectrum antibacterial activity against wound-associated pathogens, including MDR strains such as S. aureus, Pseudomonas aeruginosa, and Acinetobacter baumannii, with MICs ranging from 90 to 230 µg/mL. Its chemical composition is predominantly monoterpenes (60.75%), with α-cyclogeraniol acetate among the main constituents [41].

Anacardium genus

The species Anacardium humile A. St.-Hil. and A. occidentale L. are native to Brazil, with A. occidentale being widely used in several regions for wound healing [3, 1719, 22, 26, 27, 30]. Experimental evidence supports this traditional use, as topical application of hydroalcoholic leaf extracts of A. occidentale (1–2%) promoted wound healing in rat models, enhancing wound contraction and collagen deposition compared with control groups [42, 43].

In parallel, organic extracts from Anacardium species have demonstrated relevant antibacterial activity. Different parts of A. occidentale exhibit consistent antibacterial effects, with MIC values below 350 µg/mL. Methanolic extracts of the root bark inhibited both Gram-positive and Gram-negative bacteria, including S. aureus, Enterococcus faecalis, P. aeruginosa, and Escherichia coli, with MICs ranging from 10 to 40 µg/mL [44]. Ethanolic leaf extracts showed moderate to high activity against multiple bacterial strains (MIC 12.5–50 µg/mL) [45], while acetone extracts from nuts exhibited remarkable potency against S. aureus (MIC 0.00188–0.00375 µg/mL) [46]. In addition, acetone leaf extracts were active against Mycoplasma mycoides (MIC 310 µg/mL) [47], and hexane and methanolic extracts from aerial parts inhibited S. aureus and E. faecalis, with lower MICs observed for methanolic preparations [48].

Although less extensively studied, A. humile also exhibits antibacterial potential. Ethanolic leaf extracts inhibited the growth of S. aureus (MIC 4.1 µg/mL) and P. aeruginosa (MIC 8.2 µg/mL) [49], while tannins obtained from acetone extracts showed activity against P. aeruginosa (MIC 4.1 µg/mL) and E. faecalis (MIC 2 µg/mL) [50].

Myracrodruon genus

Myracrodruon urundeuva Allemão (Anacardiaceae), popularly known as “aroeira-do-sertão”, “aroeira-preta”, or “aroeira-do-campo”, is traditionally used to treat skin injuries, wounds, and furuncles, mainly in Northeastern Brazil [3, 1719, 22, 26]. Experimental evidence supports this traditional use, as a carbopol gel containing stem bark extract promoted greater wound contraction and collagen formation after 14 days in an excisional wound healing model in rats [51]. Similarly, a 10% cream prepared from a stem bark decoction reduced wound area and increased collagen deposition in excisional skin wounds of male Wistar rats, demonstrating efficacy in the wound repair process [52].

In addition, antibacterial effects of M. urundeuva are associated with ethanolic extracts and essential oils from the leaves, which inhibited Gram-positive and Gram-negative wound-associated pathogens, including S. aureus, Staphylococcus epidermidis, and P. aeruginosa, with MIC values ranging from 4.1 to 220 µg/mL [49, 53].

Schinus genus

Two species of the genus Schinus were reported in association with the treatment of wounds and skin disorders from selected ethnobotanical studies. Schinus molle L., a native species and known as the pepper tree (“periquiteira”), showed use in the Southern region, with flowers employed for wound treatment [30]. Schinus terebinthifolius Raddi (“aroeira-rosa”), also native, presented a higher number of records and a broader range of uses, involving different plant parts and indications such as wounds, furuncles, and skin conditions across distinct regions of the country [18, 22, 28, 29].

The aqueous extract of S. molle L. aerial parts, incorporated into a 5% hydrogel formulation, increased wound closure rates in Wistar rats, promoting re-epithelialization, fibrosis, and neovascularization in the regenerated epidermal and subepidermal tissue. Although the same extract was tested against six microorganisms, including S. aureus and S. epidermidis, antibacterial activity was observed only against Citrobacter freundii and E. faecalis (MIC 1,560 µg/mL), a concentration comparable to gentamicin but considered high in broth microdilution assays [54]. In another study, methanolic extracts from leaves, bark, and flowers were active against S. aureus (MIC 62.5–250 µg/mL) [55]. Hexane extracts from fruits inhibited M. tuberculosis (MIC 125 µg/mL), while extracts from flowers, bark, and fruits were active against Streptococcus pneumoniae (MIC 62.5–250 µg/mL) [56]. Altogether, these findings highlight the antimicrobial potential of S. molle, with bioactive compounds distributed across extracts of different polarities.

Earlier experimental evidence indicates that not all preparations of S. terebinthifolius promote wound repair. In a rat excisional wound model, topical application of a hydroalcoholic bark extract delayed re-epithelialization and resulted in larger wound areas compared with saline-treated controls, despite increased mononuclear cell infiltration at later stages [57]. In contrast, in a murine model of S. aureus—infected wounds, topical administration of an N-acetylglucosamine-binding lectin isolated from S. terebinthifolius leaves at concentrations of 32 and 64 µg/mL accelerated wound healing and reduced inflammatory markers, including IL-6, monocyte chemoattractant protein-1, tumor necrosis factor alpha (TNF-α), and vascular endothelial growth factor (VEGF) [58]. Likewise, the leaf essential oil demonstrated wound-healing activity in excisional wound models, promoting faster lesion closure through modulation of inflammation, angiogenesis, and collagen deposition [59].

Previously, Nunes et al. [58] showed that the lectin isolated from S. terebinthifolius leaves exhibited in vivo antimicrobial activity in a murine model of S. aureus—infected wounds, with a dose-dependent reduction in bacterial load and infection severity, accompanied by decreased exudate formation and local inflammation. Beyond these protein-based preparations, the ethanolic leaf extract inhibited Acinetobacter baumannii, showing 80% growth inhibition at 256 µg/mL, and bioassay-guided fractionation led to the isolation of pentagalloyl glucose. This compound displayed antibacterial activity, likely mediated by iron chelation, inhibiting both carbapenem-resistant and susceptible A. baumannii (MIC 64–256 µg/mL), as well as P. aeruginosa (MIC 16 µg/mL) and S. aureus (MIC 64 µg/mL) [60].

Himatanthus genus

The three Himatanthus species cited in ethnobotanical surveys are native and widely used in Northeastern, Northern, and Central-Western Brazil, particularly through latex and leaf preparations, reflecting a consistent cultural association with wound care across regions [19, 22, 27, 34]. This convergence suggests that wound-healing applications may represent a traditional pharmacological signature of the genus.

Several studies consistently reinforce the traditional wound-healing use of Himatanthus species. In Himatanthus drasticus (Mart.) Plumel (“sucuúba” or “janaguba”), both latex- and leaf-based preparations accelerated wound closure and enhanced fibroblast activity in murine models. Ointments containing 2% soluble latex proteins promoted complete re-epithelialization within 14 days and increased fibroblast density [61], while ethanolic leaf extracts at 50–100 mg/kg similarly improved lesion reduction and collagen deposition after 21 days [62]. Himatanthus sucuuba (Spruce ex Müll. Arg.) latex also showed reproducible regenerative effects, as twice-daily topical application for 10 days stimulated wound healing, and phytochemical profiling revealed 24 constituents, mainly flavonoids, supporting its bioactive potential [63]. Complementary findings from a 15-day treatment with H. sucuuba latex demonstrated early epithelialization, reduced inflammation, and increased collagen deposition and fibroblast abundance compared with zinc oxide cream [64]. Likewise, the ethanolic leaf extract of H. obovatus (Müll. Arg.) Woodson formulated in carbopol gel reduced lesion size and increased collagen content and fibroblast levels by day 21 [62].

Regarding antibacterial activity, only H. sucuuba has demonstrated meaningful inhibition of clinically relevant bacteria in broth microdilution assays. The aqueous latex fraction inhibited Staphylococcus species, including S. aureus, S. epidermidis, and Staphylococcus haemolyticus, at 350 µg/mL [65], whereas gallic acid isolated from this fraction showed markedly greater potency (MIC 31 µg/mL against S. aureus and S. epidermidis). Earlier studies of the methanolic root extract led to the isolation of the iridoids allamandin and plumericin, which exhibited broader antibacterial activity, with MICs ranging from 10 to 40 µg/mL against S. aureus, P. aeruginosa, and E. coli [66]. Collectively, these findings indicate that H. sucuuba may contribute to its traditional use in infected or inflamed wounds.

Aloe genus

The species of the genus Aloe recorded in ethnobotanical surveys, all exotic, are also mentioned for the care of burns, infections, and cleansing, with a predominance of leaf use. Aloe arborescens Mill. is associated with wound and burn care in the Southern region [32]. Aloe vera (L.) Burm.f. (synonym Aloe barbadensis Mill.) accounts for a total of nine ethnobotanical records, distributed across the Central-Western, Northeastern, Southeastern, and Southern regions of Brazil [1, 3, 19, 22, 23, 25, 26, 31, 33].

In vivo studies demonstrate that preparations obtained from the leaves of Aloe arborescens, when applied topically, exhibit relevant wound-healing activity in Wistar rats, both in models of third-degree burns and surgical wounds [67, 68]. Consistently, these studies indicate promotion of re-epithelialization, acceleration of wound closure, increased angiogenesis, and improved organization of collagen fibers during the tissue repair process. Extracts prepared using a dichloromethane: methanol (1:1) mixture, as well as acetone leaf extracts, demonstrated activity against H. pylori, with MIC values ranging from 130 to 250 µg/mL [69, 70], and against different enteric and Gram-positive pathogens, notably S. aureus (MIC 18 µg/mL) and Shigella flexneri (MIC 18 µg/mL) [71]. Additionally, alcoholic leaf extracts exhibited relevant antibacterial activity against S. aureus (MIC 70 µg/mL) and E. faecalis (MIC 140 µg/mL) [72].

Although several systematic reviews and meta-analyses have evaluated the efficacy of A. vera in wound healing among patients with second-degree burns [73], no meta-analyses specifically addressing the healing of non-burn cutaneous wounds were identified. In contrast, evidence from veterinary clinical studies indicates that the topical application of A. vera leaf gel in dogs and cats accelerates wound shrinkage, reduces healing time, and decreases lesion severity when compared with silver sulfadiazine [74].

Based on the selected studies, simple preparations obtained from the leaf gel and ethanolic extracts of Aloe vera showed antibacterial activity against oral pathogens, including Streptococcus mutans, Aggregatibacter actinomycetemcomitans, and Porphyromonas gingivalis, as well as against representative Gram-positive and Gram-negative bacteria, with MIC values generally below 60 µg/mL [75]. Notably, activity was also reported against multidrug-resistant P. aeruginosa and Bacillus isolates, with most of which were inhibited at concentrations ≤ 200 µg/mL [76, 77].

Calendula genus

Calendula officinalis L., an exotic species, appears in four ethnobotanical records associated with the treatment of skin lesions, burns, and scarring, with predominant use of the flowers across Northeastern, Southeastern, and Southern Brazil [19, 23, 31, 33].

The wound-healing activity of C. officinalis has been demonstrated in both clinical and experimental models. In a clinical trial involving patients with acute traumatic wounds healing by secondary intention, the topical application of a standardized 2% extract prepared from the flowers of C. officinalis significantly increased the rate of wound closure and reduced the time to complete epithelialization [78]. Complementarily, the oral administration of capsules containing 2 g of C. officinalis extract, also derived from the flowers of the species, for 14 days in patients with second-degree burns, resulted in significantly greater improvements in wound-healing scores compared with placebo [79].

Although several studies report antibacterial activity for C. officinalis, including investigations targeting periodontal pathogens [80], only the study by Larçin et al. [81] presented MIC values within the range established in this review. In that study, the methanolic flower extract exhibited an MIC of 256 µg/mL against Erwinia amylovora, a Gram-negative bacterium responsible for fire blight in apples and pears. The authors identified chlorogenic acid, caffeic acid, rutin, and salicylic acid as constituents common to both methanolic and aqueous flower extracts, with the higher relative amount of rutin in the methanolic extract correlating with its greater antibacterial activity.

Symphytum genus

Ethnobotanical studies indicate that Symphytum officinale L., an exotic species in Brazil and popularly known as confrei, is mentioned in seven surveys conducted across the Central-Western, Southeastern, Northeastern, and Southern regions of the country. The leaf is the most frequently used plant part, and the species is even reported for the treatment of infected wounds [3, 22, 23, 30, 31, 33, 34].

Preclinical studies in animal models and humans demonstrate that extracts of S. officinale accelerate wound healing through modulation of inflammatory infiltrate, significant enhancement of collagen deposition [82], and improved tissue organization associated with antioxidant activity [83]. In humans, standardized creams containing 10% of the aerial-part extract reduced abrasion healing time by nearly 3 days [84]. A more recent study using creams prepared with an ethanolic root extract (10% and 20%) accelerated regeneration in Wistar rats and identified polyphenolic compounds by LC-ESI+-MS analysis, such as salvianolic acids, rosmarinic acid, and caffeic acid, in addition to quantifying allantoin. The extract demonstrated antimicrobial activity against Gram-positive and Gram-negative bacteria; however, the MIC values reported were comparatively high, ranging from 765.38 to 6,123.01 µg/mL [85]. These findings are consistent with the limited number of studies reporting pronounced antibacterial activity for S. officinale. Although Thibane et al. [86] described lower MIC values, 98 µg/mL for methanolic and aqueous leaf extracts against E. coli, such results appear uncommon in the available literature and should be interpreted with caution until more comprehensive searches are undertaken.

Maytenus genus

Maytenus ilicifolia Mart. ex Reissek (syn. M. officinalis) and Maytenus rigida Mart., known respectively as “Espinheira-santa” [87] and “Bom-nome” [26], are native Brazilian species traditionally used for wound healing, particularly their leaves and stem barks [24, 25, 30]. Maytenus ilicifolia (syn. Maytenus officinalis) and Maytenus rigida Mart., known respectively as “espinheira-santa” [87] and “bom-nome” [26], are native Brazilian species traditionally used in wound healing, particularly through leaf and stem bark preparations [25, 26, 31]. Topical application of a hydroalcoholic leaf extract of M. ilicifolia, rich in phenolic compounds and tannins, accelerated skin wound closure in BALB/c mice at a 4% concentration, using 100 mg of ointment per wound after 3 and 7 days of treatment [88]. In addition, the polar methanolic leaf extract inhibited B. cereus (MIC 156 µg/mL) [87]. In contrast, experimental evaluation of the ethanolic bark extract of M. rigida in a rat excisional wound model did not demonstrate significant wound-healing or anti-inflammatory effects, indicating that cicatrizing activity may depend on species, plant part, or preparation method [89]. Despite these findings, antibacterial activity reported for both species against pathogens relevant to wound infections generally involved high MIC values, frequently exceeding 1,000 µg/mL [90, 91].

Croton genus

In this review, four Croton species emerged as being associated with skin problems: Croton heliotropiifolius Kunth [23, 31], Croton salutaris Casar. [1], Croton urucurana [22, 23] and Croton zehntneri Pax & K. Hoffm. [32] are used in different Brazilian regions for wound healing, skin cleansing, and the treatment of furuncles, with applications involving especially latex.

Experimental studies support the wound-healing properties traditionally attributed to Croton species as medicinal agents. Topical application of a formulation containing 20% essential oil from C. zehntneri leaves enhanced wound closure in mice by increasing fibroblast activity, angiogenesis, and collagen deposition, an effect largely attributed to its major constituent trans-anethole [92]. The ethanolic extract of C. urucurana stem bark also displays consistent regenerative effects: ointments containing 5–10% extract accelerated healing in IL-10 knockout mice, promoting fibroblast proliferation, neovascularization, and deposition of type I/III collagen [93]. In a complementary venom-induced injury model in Swiss mice, higher concentrations of the stem bark ethanolic extract (10, 20, and 40%) markedly increased lesion contraction and led to early re-epithelialization and granulation tissue formation, further confirming its pro-angiogenic and fibroblast-stimulating activity [94].

Among the evaluated species, the essential oil from aerial parts of C. heliotropiifolius was tested against several Gram-positive and Gram-negative bacterial strains; however, it exhibited antibacterial activity only against B. cereus, with a MIC of 62.5 µg/mL [95]. The ethanolic leaf extract of C. zehntneri inhibits S. aureus with a MIC of 64 µg/mL, reinforcing the traditional use of this species and the presence of phenolic metabolites, such as tannins and flavonoids, associated with antibacterial activity [96]. Its essential oil has high content of the monoterpenoid estragole (≥ 80%), which inhibits E. coli, S. aureus, Streptococcus β-haemolyticus, and S. flexneri, with MIC values below 50 µg/mL [97]. In contrast, C. urucurana exhibited a broader spectrum of action. The fresh latex, as well as the 75% ethanolic and chloroform extracts of the stem bark, showed activity against various clinically important bacteria, with MICs ranging from 125 to 250 µg/mL, including P. aeruginosa and different Staphylococcus species [98]. A recent study demonstrates the antibiofilm activity of the hexane extract, and the isolated compound α-costol from the species [99]. On the other hand, no antibacterial activity has been identified for C. salutaris.

Anadenanthera genus

Two native Brazilian species of Anadenanthera, Anadenanthera colubrina (Vell.) Brenan and Anadenanthera peregrina (L.) Speg., and their respective varieties (Anadenanthera colubrina var. cebil and Anadenanthera peregrina var. falcata) were associated with skin care and wound healing. The stem bark, particularly the inner bark, was the most frequently used plant part, although roots and resin were also reported for A. peregrina. Most citations were concentrated in the Central-West region, with only one additional record from the Northeast [1, 22, 26].

The 5% ethanolic bark extract of A. colubrina shows evidence of wound-healing activity in an animal model by topical application, with increased collagen deposition in the lesions, neutrophil infiltration, enhanced macrophage infiltration, and elevated IL-10 levels [100, 101]. The strongest evidence for the genus comes from studies demonstrating anti-S. aureus activity. The crude ethyl acetate extract from the leaves of A. colubrina var. cebil showed an IN50 of 312.5 µg/mL, and two of its isolated constituents, hyperoside and proanthocyanidin, displayed even stronger activity, with values of 62.5 µg/mL [102]. In addition, the aqueous leaf extract of A. peregrina also exhibited activity against S. aureus, with a MIC of 310 µg/mL [103].

Caesalpinia genus

The only species cited was Caesalpinia ferrea C. Mart., a native Brazilian species popularly known as “jucá or pau-ferro”, whose bark, fruits, and seeds are traditionally used in the Central-Western and Northeastern regions of the country [3, 22, 26]. Experimental studies consistently demonstrate that topical treatment with different preparations of C. ferrea, including a 12.5% ethanolic fruit extract [104], 24% pod powder [105], bark extracts and bark powder mixed with petrolatum (1:2, w/w) [106], as well as bark and pod extracts enriched with 0.1% polysaccharides (also reported as Libidibia ferrea), accelerates wound closure, reduces inflammation, and enhances collagen deposition and fibroblast proliferation in goat, rabbit, and Wistar rat wound models [107, 108].

In the study using an ointment prepared with bark mixed into petroleum jelly, the microbiological analysis performed on day 14 revealed the absence of S. aureus in comparison to the control group [105], suggesting activity against S. aureus. Consistently, methanolic and ethanolic extracts from fruits or pods showed activity against oral and clinically important bacteria, including S. mutans and E. faecalis, with MIC values within the 40–125 µg/mL range [109111].

Copaifera genus

The Copaifera species cited for wound treatment are native. Copaifera cearensis Huber ex Ducke (“copaíba”) is used in the Northeastern region for healing wounds [3], while Copaifera langsdorffii Desf. (“copaíba or “pau-d´oleo, podoi”) shows more diverse uses, including erysipelas, with different plant parts employed in the Northeastern [20] and Central-Western regions [22, 26]. Copaifera multijuga Hayne (“copaíba”), recorded in the Northern region [27], is mentioned as a skin healer based on the stem bark and stem oil.

Both C. langsdorffii oleoresin (4%) [112] and hydroalcoholic extract 10% of the leaves and 10% oleo-resin creams [113] demonstrate a beneficial effect on wound healing in Wistar rats, with the latter preparation demonstrating an anti-inflammatory activity boost in reepithelialization, angiogenesis, cell proliferation, and extracellular matrix remodeling. Subsequently, both the 10% hydroalcoholic extract and the 10% oil-resin creams exhibited wound-healing potential in horse skin wounds after 14 days [114]. In addition, the carbopol gel containing 1% C. langsdorffii accelerated wound healing in BALB/c mice [115]. In contrast, although the oleoresin of C. multijuga contributed positively to second-intention skin wound healing in Wistar rats, it was less effective than the reference agent (nitrofurazone) [116]. Nevertheless, a double-blind, randomized, and controlled clinical trial using a commercial formulation based on C. multijuga (CopaibaPolyHy-2) demonstrated significantly faster healing time, increased granulation and epithelial tissue formation, and reduced exudate [117].

The antimicrobial evidence for C. langsdorffii includes relevant activity of trunk oleoresin (MIC 200 and 125 µg/mL, respectively) [118, 119] and the ethyl acetate leaf extract (MIC 32 µg/mL) against S. aureus [120]. Furthermore, the trunk oleoresins, including those for C. multijuga, demonstrated efficacy against M. tuberculosis, with MIC values ranging from 62.5 to 250 µg/mL [121]. These findings, together with studies reporting the isolation of diterpenes from the species with activity against several Gram-positive and Gram-negative bacteria and M. tuberculosis, reinforce its broad antimicrobial potential, particularly against clinically relevant pathogens [122124].

Hymenaea genus

Hymenaea courbaril L., a native species popularly known as “jatobá” in Brazil, is traditionally used in the Northeast, where fruits, stem bark, and inner bark are applied for wound care [21, 26], and in the Center-West, where the resin is also employed alongside the bark [22]. The species’ sap accelerated wound closure, promoting fibroblast proliferation and migration and re-epithelialization by day 14 [125]. Additionally, seed-derived xyloglucan enhanced wound healing in diabetic mice by advancing re-epithelialization, improving dermal organization, and increasing type I collagen deposition [126].

The methanolic extract of the leaves exhibited substantially higher potency, with an MIC of only 16 µg/mL against S. aureus and P. aeruginosa [127]. For the stem bark, both methanolic and hexane extracts showed MIC values of 200 µg/mL against M. tuberculosis, while the hexane and dichloromethane extracts presented values ranging from 25–200 µg/mL [128]. In addition, the essential oil extracted from the fruit peels exhibited MIC values around 200 µg/mL [129]. In contrast, the hydroalcoholic extracts of the bark and starchy pulp of H. courbaril fruits exhibited moderate antibacterial activity, with MIC values of 350 µg/mL against S. aureus, E. coli, and P. aeruginosa [130]. Notably, during wound-healing assays with seed-derived xyloglucan, microbiological evaluation showed no contamination of the wound area throughout the 12-day treatment period, suggesting a protective antimicrobial effect in the wound environment [126].

Stryphnodendron genus

Stryphnodendron adstringens (Mart.) Coville, frequently referred to by its synonym Stryphnodendron barbatiman, is a native plant cited across three different regions of Brazil for the treatment of skin problems, particularly using its bark [1, 3, 18, 22, 23, 26, 28].

Multiple studies consistently demonstrate that bark extracts of S. adstringens exert a range of effects related to tissue repair in Wistar rat models, regardless of the extraction solvent employed. These include aqueous crude extracts formulated as gels [131], hydroethanolic extracts incorporated into 5% gels [132], ethyl acetate fractions obtained from acetone:water (7:3) extracts formulated as ointments or 1% gels [133, 134], and standardized formulations such as the 50% dry extract Fitoscar™ [135]. Overall, the findings indicate mechanisms that act concomitantly on the inflammatory, proliferative, and remodeling phases of wound healing, including enhanced migration of fibroblasts, stimulation of angiogenesis, and increased collagen deposition. Notably, a high concentration of proanthocyanidins was identified by mass spectrometry in the acetone:water (7:3) extract, compounds known to modulate oxidative pathways, stimulate fibroblasts, and regulate key angiogenic proteins such as VEGF [133]. In contrast, the hydroalcoholic extract was shown to be rich in phenolic constituents such as tannins and flavonoids, including gallic acid, caffeic acid, and rutin, all recognized for their anti-inflammatory potential [132].

Different preparations obtained from the bark demonstrated relevant antibacterial activity, especially against Staphylococcus spp. and bacteria associated with oral infections. The aqueous and ethanolic bark extracts showed expressive activity against pathogens such as S. aureus, S. mutans, and Actinobacillus actinomycetemcomitans, with MIC values below 60 µg/mL [136]. Subsequently, a similar potency was demonstrated in the work of Cruz et al. [137] for both the hydroalcoholic extracts of bark and leaves. On the other hand, the ethanolic bark extract and the acetone/water (7:3) bark extract, as well as the aqueous and ethyl acetate fractions obtained from the acetone/water extract, inhibited S. aureus with MIC values between 125 and 250 µg/mL [138, 139].

Sida genus

Among the four Sida species referenced for skin treatment, all are native and recorded in the Southeastern and Northeastern regions of Brazil, with predominant use of the leaves. Two of them, Sida planicaulis Cav. and Sida rhombifolia L., are traditionally employed for the treatment of furuncles [18, 20].

For S. cordifolia L., the 10% methanolic extract of the aerial parts in hydrogel improved wound contraction, collagen deposition, tensile strength, and epithelialization in diabetic Wistar rats, whereas the 10% ethanolic whole-plant ointment produced similar effects in excision, incision, and burn wound models [140, 141]. For S. rhombifolia, ointments containing ethanolic extract at 25–50% and the aqueous preparation of the leaves, applied directly, also accelerated wound healing and induced marked fibrosis and collagenization in mice [142].

The ethanol extract of S. cordifolia leaves showed antibacterial activity against B. subtilis, with a MIC of 98 µg/mL [143]. In contrast, for Sida rhombifolia, the methanol extract of the aerial parts displayed weak activity (> 500 µg/mL), and only the enriched ethyl acetate fraction demonstrated lower MIC values, such as 64 µg/mL [144]. Agar-diffusion assays reported for S. rhombifolia suggest a preliminary antibacterial trend that deserves further investigation using standardized microdilution assays; however, such findings must be interpreted cautiously given the methodological limitations inherent to diffusion-based methods [145].

Psidium genus

P. guajava L. (Myrtaceae) is widely distributed worldwide, and in Brazil, leaves, bark, and shoots are used to treat skin lesions and wound healing [17, 19, 22, 23]. An emulgel formulation with 1% of guava leaf oil, containing D-limonene, β-caryophyllene, and 1,8-cineole, enhanced wound healing in nondiabetic and diabetic Male Wistar rats. It promoted the production of collagen type I and increased superoxide dismutase, and a decrease in the expression of inflammatory cytokines and enzymes such as TNF-α, IL-1β, and IL-6. According to the authors, the 1% leaf oil emulgel formulation was considered active against Gram-positive and Gram-negative microorganisms in agar plate assays [146].

Previous reports have shown that organic leaf extracts of P. guajava obtained with a methanol–chloroform mixture (1:1) exhibited antibacterial activity against B. subtilis, with a MIC of 250 µg/mL. In the same study, a 10% (w/w) carbopol gel formulation promoted wound area contraction and faster epithelialization, achieved within 9 days [147]. Additionally, ethyl acetate and acetone leaf extracts inhibited E. coli biofilm formation, with BI50 values of approximately 60 µg/mL, and promoted complete wound closure in BALB/c mice by day 14 at doses particularly for the acetone extract [148].

Ximenia genus

The bark and inner bark of Ximenia americana L. (“ameixa, ameixeira”) have been consistently cited in ethnobotanical studies as being traditionally used for the treatment of burns and wound healing in the Northeastern region of Brazil [3, 5, 16, 33]. Experimental evidence supports these traditional uses, as hydroalcoholic extracts (2.5%) prepared from leaves, wood, and stem bark promoted the healing of surgically induced skin wounds in Wistar rats, characterized by reduced inflammatory cell infiltration and increased fibroblast proliferation [149]. In a complementary experimental model, a hydroalcoholic extract prepared from the branches of X. americana and incorporated into a 10% Lanette-based cream significantly increased the number of fibroblasts, collagen fibers, and blood vessels, accelerating the wound-healing process [150]. In the study reported by Palma et al. [149], the stem bark extract exhibited the most pronounced fibroplastic response, and phytochemical analyses revealed the presence of flavonoids, saponins, and steroids, with tannins suggested as the main compounds potentially responsible for the observed biological activities.

Notably, the most potent antibacterial activity reported for root-derived extracts was observed against enteric pathogens, including Proteus mirabilis, Shigella boydii, S. flexneri, and Salmonella typhi, with low MIC values (25–50 µg/mL) [151]. In the same study, these root fractions were also evaluated in antidiarrheal assays, supporting the relevance of their antibacterial activity against gastrointestinal pathogens. In addition, the dichloromethane root extract exhibited activity against M. tuberculosis, with a MIC value of 125 µg/mL [152].

Piper genus

Five native species of the genus Piper, Piper aduncum L., Piper amalago L., Piper gaudichaudianum Kunth, Piper peltatum L., and Piper umbellatum L., have been ethnobotanically reported as treatments for wounds, skin infections, erysipelas, and related conditions in the Northern, Northeastern, and Southern regions of Brazil [19, 27, 29].

For P. aduncum L. (“pimenta de macaco”), ointments prepared from ethanolic leaf extracts at concentrations of 5, 10, and 15% promoted wound healing in mice, reducing wound size, epithelialization time, and improving collagen fiber deposition and fibroblast scores [153]. In addition, hexane extracts obtained from the leaves and inflorescences exhibited broad-spectrum antibacterial activity against Gram-positive and Gram-negative bacteria, with notable activity of the inflorescence extract against E. coli (MIC 20 µg/mL) [154, 155] and multidrug-resistant S. aureus (MIC 16 µg/mL) [156].

Regarding P. amalago L., popularly known in Brazil as “jaborandi-manso,” a case report described the successful topical use of an aqueous leaf extract in the healing of a lacerated wound in a patient with type 2 diabetes mellitus after 15 days of treatment [157]. More recently, oral administration of an ethanolic leaf extract (100 mg/kg) in Wistar rats reduced the extent of cutaneous necrosis and improved the wound-healing process [158]. From an antimicrobial perspective, the leaf essential oil showed activity against B. cereus (MIC 313 µg/mL), while the chloroform extract inhibited Alicyclobacillus acidoterrestris with a MIC of 62.3 µg/mL, a Gram-positive bacterium of relevance to the food industry [159, 160].

P. gaudichaudianum Kunth, popularly known as “pariparoba” or “jaborandi,” lacks direct evidence supporting its use for skin wound healing. However, essential oils obtained from its aerial parts inhibited neutrophil migration in an antichemotactic assay in rats, indicating anti-inflammatory potential [161]. Although the leaf essential oil showed limited intrinsic antibacterial activity, it potentiated the effects of norfloxacin [162] and gentamicin [163] against antibiotic-resistant S. aureus, as well as gentamicin and amikacin against E. coli [164]. Additionally, it promoted biofilm disaggregation of S. aureus ATCC 25923 at concentrations ranging from 25 to 100 µg/mL [162].

P. peltatum L., popularly known in Brazil as “mão-de-macaco” or “caapeba,” demonstrated antibacterial activity against B. subtilis (MIC 31.25 µg/mL) and S. aureus (MIC 125 µg/mL) [164], as well as against A. acidoterrestris (MIC/MBC 15.62 µg/mL) [165]. However, despite its traditional use for treating erysipelas [26], no experimental evidence has been reported for activity against Streptococcus pyogenes, the classical etiological agent of this condition.

Finally, although hydroethanolic leaf extracts of P. umbellatum L. (syn. Pothomorphe umbellata), known in Brazil as “pariparoba,” have demonstrated healing activity in chronic ulcer models [166], studies evaluating its wound-healing activity are lacking. Nevertheless, its essential oils exhibited antibacterial activity against S. aureus (MIC 156 µg/mL) [167], and a benzene extract yielded the alkaloid N-benzoylmescaline, which showed remarkable activity against H. pylori (MIC 2.5 µg/mL) [168].

Plantago genus

Three species of the genus Plantago were cited: Plantago major L. (“tansagem”), Plantago sparsiflora Michx. (“tanchagem”), and Plantago tomentosa Lam. (“tansagem-silvestre, língua-de-vaca”), for the treatment of wounds and skin conditions in Brazil. P. major L., an exotic species, showed the highest number of records, with leaf use reported in the Northeastern and Southeastern regions [19, 23], whereas P. sparsiflora Michx. was cited in the Central-Western region with the use of different plant parts [21]. P. tomentosa Lam., a native species, showed a more localized use in the Southern region, restricted to the leaves [33].

A topical 10% (v/v) hydroalcoholic extract of P. major was reported to reduce wound size in patients with chronic ulcers, including diabetic foot and pressure ulcers [169]. Similarly, a 10% ointment prepared from aqueous leaf and branch extracts, applied to patients with second-degree burn injuries, resulted in wound recovery comparable to the control group; notably, by day seven, all wound cultures were negative, suggesting an antiseptic contribution to the healing process [170].

For P. tomentosa, an ethanolic leaf extract demonstrated wound-healing activity in a postoperative model in female dogs, with reduced incision length and improved epithelialization, accompanied by fewer inflammatory signs such as pain, secretion, and erythema [171]. These effects were associated with the presence of flavonoids, compounds known for their anti-inflammatory and regenerative properties.

In contrast, antibacterial evidence for P. tomentosa remains scarce, and no studies reporting MIC values within the established cutoff (≤ 350 µg/mL) were identified. Conversely, robust antibacterial activity has been reported for P. major, whose hydroethanolic leaf and root extracts, rich in phenolic compounds such as quercetin 7-rutinoside and dicaffeoylquinic acid, were active against E. coli and Klebsiella pneumoniae, with MIC values ranging from 2 to 4 µg/mL, as well as notable antibiofilm activity (MIC 2 µg/mL) [172].

Solanum genus

Of the five Solanum species associated with wound care and skin problems, the native Solanum americanum (“erva-moura”), Solanum aculeatissimum (“joá or rebenta-boi”), and Solanum scapsicoides (“arrebenta-cavalo”) stand out, whereas the exotic Solanum lycopersicum (“tomate”) and S. tuberosum are mentioned only occasionally for erysipelas and burns, with uses ranging from the fruits to the whole plant [18, 20, 23, 27, 29, 31].

Consistent experimental evidence of wound-healing activity was identified for S. lycopersicum and S. tuberosum. In the case of S. tuberosum, experimental studies were conducted in murine models of excisional wounds and burns, as well as in human clinical trials involving burn injuries. These studies generally employed preparations derived from the tubers, typically ethanolic extracts incorporated into 1–2% ointments [173, 174], or boiled or triturated potato peel applied directly as a biological dressing on burns [175, 176]. The studies demonstrated a significant acceleration in wound closure accompanied by reduced inflammation, with indications that steroidal glycoalkaloids may be involved in this response [176]. Additionally, greater fibroblast organization, enhanced collagen deposition, and faster epithelialization were observed when compared with both negative and positive controls. These effects have been attributed to the high concentration of phenolic and flavonoid compounds in tubers, such as chlorogenic acid [174]. In burn models, similar outcomes were observed, including reorganization of epidermal layers, increased granulation tissue, and improved alignment of collagen fibers [173].

For S. lycopersicum, in vivo models using cherry tomato extracts incorporated into topical gels showed a significant increase in wound contraction, particularly with 16% formulations, as well as improved histological organization of the skin in Wistar rats, with lycopene, an intense antioxidant compound, being suggested as the active constituent [177].

In contrast, S. americanum, a species occurring in Brazil, showed significant wound-healing activity of the aqueous extract from its aerial parts in open wound models in rabbits and calves, characterized by reduced inflammation, accelerated wound contraction, and increased collagen deposition. In addition, the extract was evaluated against Gram-positive and Gram-negative bacteria, and an antiseptic effect was suggested, attributed to the presence of glycoalkaloids and saponins, although antibacterial activity was observed only at relatively high concentrations (> 1,000 µg/mL) [178].

The antibacterial activity was observed for aqueous and ethanolic fruit extracts of S. lycopersicum against B. cereus, with an MIC of 130 µg/mL isolated from wound patients in hospitals in Nigeria [179]. In the case of S. tuberosum, the methanolic extract of the tubers showed MIC values of 312 µg/mL against E. coli, P. aeruginosa, and S. aureus [180]. A more recent study also identified antimicrobial activity of anthocyanins extracted from pigmented tubers against both Gram-positive and Gram-negative bacteria, with MICs ranging from 16 to 250 µg/mL [181].

General considerations on evidence coherence and research gaps

The synthesis conducted in this review, based on ethnobotanical surveys selected from different regions of Brazil, revealed a consistent set of 22 genera traditionally used in the treatment of wounds, burns, and other cutaneous conditions of possible bacterial etiology.

In absolute numbers (Figure 2), Fabaceae and Anacardiaceae accounted for the largest concentration of species with confirmed antibacterial activity, followed by Piperaceae and Euphorbiaceae, suggesting a broader taxonomic representation of antibacterial evidence within these families. When proportional distribution was considered, Fabaceae (80%), Anacardiaceae and Euphorbiaceae (75%) maintained a high representation of active species, while Piperaceae exhibited consistent activity across all evaluated taxa (100%). Intermediate proportional representation of species demonstrating antibacterial activity was observed for Malvaceae and Amaranthaceae (50% each), Solanaceae (40%), and Plantaginaceae (33.3%). These patterns may also reflect the phytochemical diversity characteristics of these families, particularly their richness in major classes of bioactive natural products, such as phenolics, alkaloids, and terpenoids. However, the considerable heterogeneity in extraction procedures, experimental models, antimicrobial assays, and extract composition limits the possibility of drawing definitive taxonomic conclusions.

Conceptual representation linking ethnobotanical knowledge to pharmacological evidence. A total of 51 medicinal plant species traditionally used in Brazil for wounds, burns, and other skin conditions were identified from ethnobotanical surveys. Literature analysis of antimicrobial dilution assays using crude extracts, essential oils, or oleoresins (MIC ≤ 350 µg/mL) indicates that approximately 40% of the species exhibit activity against S. aureus, with notable representation in Fabaceae, Anacardiaceae, Piperaceae, and Euphorbiaceae. Experimental studies further report antibacterial mechanisms including biofilm inhibition, membrane disruption, virulence factor interference, and metabolic suppression.

Regarding antibacterial activity (Figure 2), approximately 40% of the species selected from the ethnobotanical studies exhibited MIC values against S. aureus, a classical pathogen associated with skin and wound infections, and/or E. coli. In general, nonpolar extracts or essential oils obtained mainly from leaves and bark, belonging to the families Anacardiaceae, Fabaceae, and Piperaceae, showed the lowest MIC values (Supplementary material).

Among the studies providing experimental evidence of antibacterial mechanisms (Figure 2), disruption of bacterial membrane integrity was mainly reported for hydroalcoholic and ethanolic leaf extracts of Aloe arborescens and P. peltatum [72, 165], whereas suppression of bacterial metabolic activity was demonstrated for hydroalcoholic extracts of A. arborescens, organic leaf extracts of P. guajava, and hydroalcoholic extracts of C. ferrea [72, 109, 148]. Inhibition of biofilm formation was also recurrent, particularly for crude oleoresin of Copaifera langsdorffii, hydroalcoholic extracts of Croton spp., organic leaf extracts of Psidium guajava, and the essential oil of Piper gaudichaudianum [99, 123, 148, 162]. Additional mechanisms, such as interference with bacterial virulence factors, including adhesion and acidogenicity, were reported for ethanolic leaf extracts of Piper aduncum [155], while molecular recognition involving interactions with bacterial cell wall components was demonstrated for leaf-derived lectins obtained from aqueous protein extracts of Schinus terebinthifolius [58].

From a methodological perspective, this review prioritized studies evaluating the antibacterial activity of crude extracts, as these preparations are more consistent with traditional forms of use, such as infusions and tinctures. Although investigations involving fractions or isolated compounds provide relevant mechanistic insights, they were not central to the primary objective of this review and were therefore considered only as complementary evidence supporting plausible antibacterial mechanisms.

Cultural transmission and traditional methods of plant preparation and collection may significantly influence the pharmacological outcomes observed in experimental studies. The intergenerational transmission of traditional knowledge may function as an empirical selection process for species with therapeutic potential, contributing to the recurrence of certain plants in local practices. Many ethnobotanical reports describe preparations such as teas, infusions, decoctions, and tinctures, as well as topical applications such as poultices and macerations, which primarily extract polar or moderately polar compounds from medicinal plants. Antibacterial susceptibility assays, in turn, are conducted in aqueous media, requiring that crude extracts exhibit a certain degree of hydrophilicity to demonstrate activity. However, experimental studies do not always employ preparations obtained with solvents compatible with traditional modes of use. In addition, factors such as season of collection, harvesting time, and plant part used may influence chemical composition and, consequently, pharmacological outcomes. Therefore, closer alignment between traditional practices and experimental designs may enhance the translational relevance of ethnopharmacological research.

Analysis of wound-healing studies from the medicinal plants included in this review indicates that most investigations assessed antibacterial potential indirectly through broth microdilution assays for determination of MIC, particularly for essential oils or ethanolic extracts, with emphasis on activity against S. aureus [51, 115]. In contrast, relatively few studies performed functional evaluations considering bacterial load control or the absence of wound-bed contamination throughout treatment. Notably, H. courbaril, as well as topical formulations containing C. officinalis and C. ferrea, demonstrated maintenance of infection-free wounds or significant reduction of bacterial colonization during the experimental period, even in the absence of direct MIC determination [105, 126, 169].

It was observed that, among the 51 plant species analyzed (Figure 2), more than 50% (n = 28) presented evidence for both antibacterial and wound healing activities, such as Alternanthera brasiliana, A. occidentale, Myracrodruon urundeuva, Aloe vera, Calendula officinalis, Caesalpinia ferrea, Hymenaea courbaril, and Psidium guajava. Traditional uses converge with pharmacological expectations, as wound infection remains one of the main complications associated with impairment of the healing process.

On the other hand, a smaller group of species presented restricted evidence for antibacterial activity (15.7%) (Figure 2), such as Anacardium humile, Croton heliotropiifolius, Anadenanthera peregrina, Piper peltatum, or exclusively to wound-healing activity (11.8%), such as Himatanthus drasticus, Sida rhombifolia, and Plantago tomentosa, when considering the MIC value criteria adopted in this review.

Finally, approximately 17.6% of the species (Figure 2), such as Alternanthera dentata, Alternanthera ramosissima, Croton salutaris, Copaifera cearensis, Sida planicaulis, Plantago sparsiflora, Solanum aculeatissimum, and S. capsicoides, lacked experimental evidence for either antibacterial or wound-healing activity. This highlights significant gaps in pharmacological validation despite their recurrent citation in ethnobotanical surveys.

Considering the evidence discussed above, although studies on these plants suggest convergence of biological effects, relevant gaps persist in the investigation of the wound-healing and antibacterial potential of medicinal plants. There is a predominance of exploratory and screening-based studies relying on non-standardized extracts, often lacking detailed phytochemical characterization, which limits comparability across studies and compromises the reproducibility of findings related to antibacterial activity, even when such approaches are considered appropriate for early stages of investigation. In this context, the limited adoption of standardized extracts and marker-oriented phytochemical approaches represents a critical barrier to advancing the field, as the identification of chemical or biological markers associated with antibacterial activity and key wound-healing outcomes would enable a more robust linkage between extract composition and biological effects. Moreover, in vivo models that simultaneously evaluate the healing of infected wounds remain scarce, restricting the understanding of the actual contribution of antibacterial activity to tissue repair processes.

As integrative reviews can summarize heterogeneous study designs, they are inherently susceptible to selection and interpretative biases. The search was limited to three databases, and data extraction was performed by a single author. In addition, methodological differences among the included studies, such as variations in experimental models and extract preparations, may limit comparability across findings. Furthermore, publication bias and language restrictions may have influenced the representativeness of the included evidence [182].

Conclusions

This review demonstrates that Brazil holds a culturally rich and functionally coherent body of traditional knowledge related to the use of medicinal plants for the treatment of wounds, burns, and other cutaneous conditions of possible bacterial etiology. By mapping ethnobotanical studies from different regions of the country, a total of 51 plant species were identified, most of them native and associated with locally transmitted knowledge. Beyond reflecting botanical diversity, these findings highlight the existence of a consolidated cultural repertoire focused on skin-related therapeutic practices, suggesting the relevance of the country as a source of traditional knowledge systems regarding the management of wounds and cutaneous infections.

The results support a coherence between traditional use and the available pharmacological evidence when assessed under the criteria adopted in this review, particularly regarding experimental conditions and cutoff values for antibacterial activity. Moreover, although the search strategy adopted in this review was not specifically directed toward the combined evaluation of antibacterial and wound-healing activities.

Future investigations should prioritize the use of chemically standardized extracts with defined bioactive markers to ensure reproducibility and pharmacological consistency. Antibacterial evaluation should encompass panels of both susceptible and resistant clinical strains, combined with mechanistic studies aimed at elucidating modes of action and targeting bacterial adaptive resistance mechanisms, including those associated with biofilm formation, as well as testing in mature multispecies biofilm models. Achieving meaningful translational progress will require the integration of in vivo infected wound models capable of linking antimicrobial effects to measurable wound-healing outcomes. Additionally, the development of advanced topical delivery systems may enhance clinical applicability, particularly through sustained and localized release strategies, such as the incorporation of nanostructured lipid carriers within gel-based matrices to optimize drug stability, tissue penetration, and accelerated tissue repair.

Considering that skin infections represent frequent health problems in primary care and that medicinal plants remain widely used in Brazil, this review provides a structured evidence base that may support research prioritization and evidence-informed discussions in public health contexts. By delineating which traditionally used species present convergent antibacterial evidence, the findings inform future translational perspectives related to the rational use of phytotherapy in primary health care.

Abbreviations

A. occidentale L.: Anacardium occidentale L.

MIC: minimum inhibitory concentration

S. aureus: Staphylococcus aureus

TNF-α: tumor necrosis factor alpha

VEGF: vascular endothelial growth factor

Supplementary materials

The supplementary table for this article is available at: https://www.explorationpub.com/uploads/Article/file/1008164_sup_1.pdf.

Declarations

Author contributions

BBC: Conceptualization, Writing—original draft, Writing—review & editing. The author read and approved the submitted version.

Conflicts of interest

The author declares that there are no conflicts of interest.

Ethical approval

Not applicable.

Consent to participate

Not applicable.

Consent to publication

Not applicable.

Availability of data and materials

Not applicable.

Funding

Not applicable.

Copyright

© The Author(s) 2026.

Publisher’s note

Open Exploration maintains a neutral stance on jurisdictional claims in published institutional affiliations and maps. All opinions expressed in this article are the personal views of the author(s) and do not represent the stance of the editorial team or the publisher.

References

Morbeck de Oliveira AK, Matias R, Mesquita Dourado D, Matheus Fernandes R, de Araújo Abreu CA, Feliciano de Lima Silva BC. Ethnobotanical survey of medicinal species used in Taboco Village, Maracaju Mountains, Brazil, and healing activity of the species with higher value of use (Maytenus ilicifolia). Bol Latinoam Caribe Plant Med Aromat. 2023;22:53759. [DOI]
Gouveia BDLA, Albuquerque AM, Oliveira SHDS, Silva APD, Oliveira LBP, Costa MML. Tratamento de feridas: práticas empíricas sob o ponto de vista cultural e religioso. Rev Enferm UFPE On Line. 2015;9:704654.
Souza DR, Rodrigues ECAM de S. Plantas medicinais: indicação de raizeiros para o tratamento de feridas. Rev Bras Promoç Saúde. 2016;29:197203. [DOI]
Tottoli EM, Dorati R, Genta I, Chiesa E, Pisani S, Conti B. Skin Wound Healing Process and New Emerging Technologies for Skin Wound Care and Regeneration. Pharmaceutics. 2020;12:735. [DOI] [PubMed] [PMC]
Pereira-Franchi EPL, Barreira MRN, Costa NSLMD, Fortaleza CMCB, Cunha MLRSD. Prevalence of and risk factors associated with the presence of Staphylococcus aureus in the chronic wounds of patients treated in primary health care settings in Brazil. Rev Soc Bras Med Trop. 2017;50:8338. [DOI] [PubMed]
Óbitos por queimaduras no Brasil: análise inicial dos dados do sistema de informações sobre Mortalidade, 2015–2020 [Internet]. [cited 2025 Oct 15]. Available at: https://www.gov.br/saude/pt-br/centrais-de-conteudo/publicacoes/boletins/epidemiologicos/edicoes/2022/boletim-epidemiologico-vol-53-no47/view
Ruiz PBO, Lima AFC. Custos diretos médios da assistência ambulatorial, hospitalar e domiciliar prestada aos pacientes com feridas crônicas. Rev Esc Enferm USP. 2022;56:e20220295. [DOI]
Olsson M, Järbrink K, Divakar U, Bajpai R, Upton Z, Schmidtchen A, et al. The humanistic and economic burden of chronic wounds: A systematic review. Wound Repair Regen. 2019;27:11425. [DOI] [PubMed]
Cruciol Rodrigues MA, Tanita MT, Alfaro AJY, Grion CMC. Patient care for burn victims in Brazil: A national survey. Burns. 2024;50:107192. [DOI] [PubMed]
Shen AZ, Taha M, Ghannoum M, Tyring SK. Biofilms and Chronic Wounds: Pathogenesis and Treatment Options. J Clin Med. 2025;14:7784. [DOI] [PubMed] [PMC]
Nascimento JHFD, Souza Filho BM, Tomaz SC, Vieira ATS, Silva Neto MMD, Andrade AB, et al. Self-inflicted burns in Brazil: systematic review and meta-analysis. Rev Col Bras Cir. 2024;51:e20243665. [DOI] [PubMed] [PMC]
Chibante CLDP, Santo FHDE, Santos TDD, Porto IS, Daher DV, Brito WDAPD. Saberes e práticas no cuidado centrado na pessoa com feridas. Esc Anna Nery. 2017;21:e20170036. [DOI]
Angelini P. Plant-Derived Antimicrobials and Their Crucial Role in Combating Antimicrobial Resistance. Antibiotics (Basel). 2024;13:746. [DOI] [PubMed] [PMC]
Antonio Pereira I, Judah Cury B, Kaio Silva Nunes R, Mota da Silva L. Traditional Plants Used in Southern Brazil as a Source to Wound Healing Therapies. Chem Biodivers. 2023;20:e202201021. [DOI] [PubMed]
Aromataris E, Munn Z, editors. JBI manual for evidence synthesis. Adelaide: The Joanna Briggs Institute; 2020. [DOI]
Cos P, Vlietinck AJ, Berghe DV, Maes L. Anti-infective potential of natural products: how to develop a stronger in vitro ‘proof-of-concept’. J Ethnopharmacol. 2006;106:290302. [DOI] [PubMed]
Almeida BV, Ribeiro DA, Santos MO, Macêdo DG, Macedo JGF, Macêdo MJF, et al. Mixtures of medicinal plants from Caatinga: basis for further bioprospecting studies. South Afr J Bot. 2022;151:15877. [DOI]
Santana BF, Voeks RA, Funch LS. Quilombola ethnomedicine: the role of age, gender, and culture change. Acta Bot Bras. 2022;36:e2020abb0500. [DOI]
P Sousa EA, Mendonça ACAM, Garcia ÍR, N Lisboa MA, Kamdem JP, Cruz GV, et al. Ethnoknowledge of medicinal and mystical plants used by healers in Juazeiro do Norte, Ceará, Northeast Brazil. Indian J Tradit Know. 2021;20:15466.
Yazbek PB, Matta P, Passero LF, Santos GD, Braga S, Assunção L, et al. Plants utilized as medicines by residents of Quilombo da Fazenda, Núcleo Picinguaba, Ubatuba, São Paulo, Brazil: A participatory survey. J Ethnopharmacol. 2019;244:112123. [DOI] [PubMed]
Macêdo MJF, Ribeiro DA, de Oliveira Santos M, de Macêdo DG, Macedo JGF, de Almeida BV, et al. Fabaceae medicinal flora with therapeutic potential in savanna areas in the Chapada do Araripe, northeastern Brazil. Rev Bras Farmacogn. 2018;28:73850. [DOI]
Ribeiro RV, Bieski IGC, Balogun SO, Martins DTO. Ethnobotanical study of medicinal plants used by Ribeirinhos in the North Araguaia microregion, Mato Grosso, Brazil. J Ethnopharmacol. 2017;205:69102. [DOI] [PubMed]
Borges BS, Dutra AG, Tenório IFP, Mendonça ARA. Levantamento etnobotânico de plantas medicinais utilizadas na cicatrização de feridas. Rev Bras Pl Med. 2016;18:85867. [DOI]
Crepaldi CG, Campos JLA, Albuquerque UP, Sales MF. Richness and ethnobotany of the family Euphorbiaceae in a tropical semiarid landscape of Northeastern Brazil. South Afr J Bot. 2016;102:15765. [DOI]
de Lima CAB, Lima ARA, Mendonça CV, Lopes CV, Heck RM. O uso das plantas medicinais e o papel da fé no cuidado familiar. Rev Gaúcha Enferm. 2016;37:e68285. [DOI]
do Nascimento MWA, Veríssimo RCSS, de Assis Bastos ML, Bernardo THL. Indicações de plantas medicinais realizadas por raizeiros para tratamento de feridas. Rev Eletr Enf. 2016;18:e1152. [DOI]
Pedrollo CT, Kinupp VF, Shepard G Jr, Heinrich M. Medicinal plants at Rio Jauaperi, Brazilian Amazon: Ethnobotanical survey and environmental conservation. J Ethnopharmacol. 2016;186:11124. [DOI] [PubMed]
de Santana BF, Voeks RA, Funch LS. Ethnomedicinal survey of a maroon community in Brazil’s Atlantic tropical forest. J Ethnopharmacol. 2016;181:3749. [DOI] [PubMed]
Bolson M, Hefler SM, Dall’Oglio Chaves EI, Gasparotto Junior A, Cardozo Junior EL. Ethno-medicinal study of plants used for treatment of human ailments, with residents of the surrounding region of forest fragments of Paraná, Brazil. J Ethnopharmacol. 2015;161:110. [DOI] [PubMed]
Bieski IG, Leonti M, Arnason JT, Ferrier J, Rapinski M, Violante IM, et al. Ethnobotanical study of medicinal plants by population of Valley of Juruena Region, Legal Amazon, Mato Grosso, Brazil. J Ethnopharmacol. 2015;173:383423. [DOI] [PubMed]
Piriz MA, Ramos AR, Lopes CV, Silva MM, Heck RM, Barbieri RL. Uso popular de plantas medicinais na cicatrização de feridas: implicações para a enfermagem. Rev Enferm UERJ. 2015;23:6749.
Saraiva ME, Ulisses AV, Ribeiro DA, de Oliveira LG, de Macêdo DG, de Sousa Fde F, et al. Plant species as a therapeutic resource in areas of the savanna in the state of Pernambuco, Northeast Brazil. J Ethnopharmacol. 2015;171:14153. [DOI] [PubMed]
Tribess B, Pintarelli GM, Bini LA, Camargo A, Funez LA, de Gasper AL, et al. Ethnobotanical study of plants used for therapeutic purposes in the Atlantic Forest region, Southern Brazil. J Ethnopharmacol. 2015;164:13646. [DOI] [PubMed]
Vieira LS, Sousa RS, Lemos JR. Plantas medicinais conhecidas por especialistas locais de uma comunidade rural maranhense. Rev Bras Pl Med. 2015;17:10618. [DOI]
Marchete R, Oliveira S, Bagne L, Silva JIS, Valverde AP, Aro AA, et al. Anti-inflammatory and antioxidant properties of Alternanthera brasiliana improve cutaneous wound healing in rats. Inflammopharmacology. 2021;29:144358. [DOI] [PubMed]
Barua CC, Ara Begum S, Talukdar A, Datta Roy J, Buragohain B, Chandra Pathak D, et al. Influence of Alternanthera brasiliana (L.) Kuntze on Altered Antioxidant Enzyme Profile during Cutaneous Wound Healing in Immunocompromised Rats. ISRN Pharmacol. 2012;2012:948792. [DOI] [PubMed] [PMC]
de Araújo AD, de Barros Pimentel MD, Santos CDS, Silva RA, Cadena PG, Silva NH, et al. Aqueous extract of fresh leaves from Alternanthera brasiliana (L.) Kuntze: chemical evaluation and antimycobacterial and anticandidal activities. Adv Tradit Med. 2021;21:76777. [DOI]
TrivellatoGrassi L, Malheiros A, Meyre-Silva C, Buss Zda S, Monguilhott ED, Fröde TS, et al. From popular use to pharmacological validation: a study of the anti-inflammatory, anti-nociceptive and healing effects of Chenopodium ambrosioides extract. J Ethnopharmacol. 2013;145:12738. [DOI] [PubMed]
Sérvio EML, de Araújo KS, Silva Nascimento LR, Costa CLS, Mendes LMS, Maia Filho ALM, et al. Cicatrização de feridas com a utilização do extrato de Chenopodium ambrosioides (mastruz) e cobertura secundária estéril de gaze em ratos. ConScientiae Saúde. 2011;10:4418.
Silva LI, Karuppusamy A, Miyajima F, Violante IMP, Bieski IGC, Balogun SO, et al. Antimicrobial and antioxidant activities of selected plants used by populations from Juruena Valley, Legal Amazon, Brazil. Int J Pharm Pharm Sci. 2017;9:17991. [DOI]
Azghar A, Dalli M, Loukili EH, Belbachir Y, Tahri M, Benaissa E, et al. Evaluation of the antibacterial activity of essential oil of Dysphania ambrosioides (L.) Mosyakin and Clemants against clinical multidrug-resistant bacteria. Asian J Plant Sci. 2023;22:7581. [DOI]
Nehete M, De S, Degani M, Tatke P. A topical formulation of Anacardium occidentale L. leaves extract enhances wound healing via mediating TNF-α and TGF-β. Indian J Exp Biol. 2023;61:42435. [DOI]
Kumari MK, Vittalrao AM, Charitha C, Praveen Kumar PSE, Prabhath S. Evaluation of wound healing activity of an ethanolic extract of Anacardium occidentale leaves in Wistar rats. Biomed Pharmacol J. 2020;13:20618. [DOI]
Chekwube AC, Jude AI, Chijioke OR, Nonye UT, Hannah ON, Celestine UO, et al. Phytochemical screening and antibacterial evaluation of Anacardium occidentale root collected in Agbani, Eastern Nigeria. J Adv Med Pharm Sci. 2023;25:3948. [DOI]
Sebastian J, Thomas N, Raj PR, Johns BG, Chacko AJ, Daisy PA. Formulation and evaluation of herbal gel containing the leaf extract of Anacardium occidentale. Int J Pharm Sci Rev Res. 2020;61:937.
Parasa LS, Sunita T, Rao KB, Rao AH, Rao JS, Kumar L. Acetone extract of cashew (Anacardium occidentale L.) nut shell liquid against methicillin-resistant Staphylococcus aureus (MRSA) by minimum inhibitory concentration (MIC). J Chem Pharm Res. 2011;3:73642.
Muraina IA, Adaudi AO, Mamman M, Kazeem HM, Picard J, McGaw LJ, et al. Antimycoplasmal activity of some plant species from northern Nigeria compared to the currently used therapeutic agent. Pharm Biol. 2010;48:11037. [DOI] [PubMed]
Madureira AM, Ramalhete C, Mulhovo S, Duarte A, Ferreira MJ. Antibacterial activity of some African medicinal plants used traditionally against infectious diseases. Pharm Biol. 2012;50:4819. [DOI] [PubMed]
Maia CNS, Silva CM, Júnior RR, Oliveira DA, Ferreira PRB, Godinho CS, et al. Antimicrobial activities and preliminary phytochemical tests of crude extracts of important ethnopharmacological plants from Brazilian Cerrado. J Med Plants Res. 2016;10:61220. [DOI]
Ferreira PRB, Mendes CSO, Rodrigues CG, Rocha JCM, de Andrade Royo V, Valério HM, et al. Antibacterial activity tannin-rich fraction from leaves of Anacardium humile. Ciência Rural. 2012;42:186164. [DOI]
Pires Rodrigues de Almeida Ribeiro F, Fernandes Matos L, Brito Queiroz D, Botelho MA, de Souza Siqueira Barreto DR, Santana de Lima R, et al. Wound Healing Effect of Lippia sidoides and Myracrodruon urundeuva Nanogel. Chem Biodivers. 2024;21:e202302043. [DOI] [PubMed]
Teixeira MC, Lopes MJP, de Sousa-Júnior DL, Ribeiro AES, Pereira BS, de Aquino PEA, et al. Evaluation of the healing potential of Myracrodruon urundeuva in wounds induced in male rats. Rev Bras Farmacogn. 2020;30:21423. [DOI]
de Araújo ÍDR, de Aquino ND, de Aguiar Guerra ACV, de Almeida Júnior RF, Mendonça Araújo R, de Araújo Júnior RF, et al. Chemical composition and evaluation of the antibacterial and cytotoxic activities of the essential oil from the leaves of Myracrodruon urundeuva. BMC Complement Altern Med. 2017;17:419. [DOI]
Aboalhaija N, Afifi F, Al-Hussaini M, Al-Najjar M, Abu-Dahab R, Hasen E, et al. In vitro and in vivo evaluation of the wound healing potential of the extracts of Schinus molle L. (Anacardiaceae) grown in Jordan. Indian J Pharm Sci. 2021;83:26170.
Salazar-Aranda R, Pérez-López LA, López-Arroyo J, Alanís-Garza BA, Waksman de Torres N. Antimicrobial and antioxidant activities of plants from northeast of Mexico. Evid Based Complement Alternat Med. 2011;2011:536139. [DOI] [PubMed] [PMC]
Molina-Salinas GM, Pérez-López A, Becerril-Montes P, Salazar-Aranda R, Said-Fernández S, de Torres NW. Evaluation of the flora of northern Mexico for in vitro antimicrobial and antituberculosis activity. J Ethnopharmacol. 2007;109:43541. [DOI] [PubMed]
Branco Neto ML, Ribas Filho JM, Malafaia O, Oliveira Filho MA, Czeczko NG, Aoki S, et al. Evaluation of hydroalcoholic extract of Aroeira (Shinus Terebinthifolius Raddi) in the healing process of wound skin in rats. Acta Cir Bras. 2006;21 Suppl 2:1722. Portuguese. [DOI] [PubMed]
Nunes MAS, Silva LDS, Santos DM, Cutrim BDS, Vieira SL, Silva ISS, et al. Schinus terebinthifolius Leaf Lectin (SteLL) Reduces the Bacterial and Inflammatory Burden of Wounds Infected by Staphylococcus aureus Promoting Skin Repair. Pharmaceuticals (Basel). 2022;15:1441. [DOI] [PubMed] [PMC]
Estevão LRM, Simões RS, Cassini-Vieira P, Canesso MCC, Barcelos LDS, Rachid MA, et al. Schinus terebinthifolius Raddi ( Aroeira) leaves oil attenuates inflammatory responses in cutaneous wound healing in mice 1. Acta Cir Bras. 2017;32:72635. [DOI] [PubMed]
Dettweiler M, Marquez L, Lin M, Sweeney-Jones AM, Chhetri BK, Zurawski DV, et al. Pentagalloyl glucose from Schinus terebinthifolia inhibits growth of carbapenem-resistant Acinetobacter baumannii. Sci Rep. 2020;10:15340. [DOI] [PubMed] [PMC]
Souza TFG, Ramos MV, Pierdoná TM, Rabelo LMA, Vasconcelos MS, Carmo LD, et al. Wound tissue remodeling by latex exudate of Himatanthus drasticus: A plant species used in Brazilian folk medicine. Heliyon. 2023;9:e21843. [DOI] [PubMed] [PMC]
Santos WW, de Almeida PM, Alves WS, Bacelar LL, Maia Filho ALM, de Oliveira MDD A, et al. O efeito cicatrizante do extrato etanólico das folhas de Himatanthus obovatus (Müll Arg.) Woodson. Res Soc Dev. 2021;10:e29010817461. [DOI]
Herrera-Calderón O, Calero-Armijos LL, Cardona-G W, Herrera-R, Moreno G, Algarni MA, et al. Phytochemical Screening of Himatanthus sucuuba (Spruce) Woodson (Apocynaceae) Latex, In Vitro Cytotoxicity and Incision Wound Repair in Mice. Plants (Basel). 2021;10:2197. [DOI] [PubMed] [PMC]
Calero-Armijos LL, Herrera-Calderon O, Arroyo-Acevedo JL, Rojas-Armas JP, Hañari-Quispe RD, Figueroa-Salvador L. Histopathological evaluation of latex of Bellaco-Caspi, Himatanthus sucuuba (Spruce) Woodson on wound healing effect in BALB/C mice. Vet World. 2020;13:10459. [DOI] [PubMed] [PMC]
Silva JRA, Rezende CM, Pinto AC, Amaral ACF. Cytotoxicity and antibacterial studies of iridoids and phenolic compounds isolated from the latex of Himatanthus sucuuba. Afr J Biotechnol. 2010;9:735760.
Morel AF, Graebner IB, Porto C, Dalcol II. Study on the antimicrobial activity of Hymatanthus sucuba. Fitoterapia. 2006;77:503. [DOI] [PubMed]
Ghane F, Rasouli P, Khanjari B, Yousofi A, Zarenezhad A, Fattahi H, et al. Antimicrobial activity and wound healing properties of Aloe arborescens extract: an in vivo study. J Adv Biomed Sci. 2023;13:13847. [DOI]
Jia Y, Zhao G, Jia J. Preliminary evaluation: the effects of Aloe ferox Miller and Aloe arborescens Miller on wound healing. J Ethnopharmacol. 2008;120:1819. [DOI] [PubMed]
Dinat S, Orchard A, van Vuuren S. Antimicrobial activity of Southern African medicinal plants on Helicobacter pylori and Lactobacillus species. J Ethnopharmacol. 2024;330:118238. [DOI]
Shirinda H, Leonard C, Candy G, van Vuuren S. Antimicrobial activity and toxicity profile of selected southern African medicinal plants against neglected gut pathogens. S Afr J Sci. 2019;115:110. [DOI]
Bisi-Johnson MA, Obi CL, Samuel BB, Eloff JN, Okoh AI. Antibacterial activity of crude extracts of some South African medicinal plants against multidrug resistant etiological agents of diarrhoea. BMC Complement Altern Med. 2017;17:321. [DOI] [PubMed] [PMC]
Maliehe TS, Nqotheni MI, Shandu JS, Selepe TN, Masoko P, Pooe OJ. Chemical Profile, Antioxidant and Antibacterial Activities, Mechanisms of Action of the Leaf Extract of Aloe arborescens Mill. Plants (Basel). 2023;12:869. [DOI] [PubMed] [PMC]
Huang Y, Chen KC, Wang JH, Lin YK. Effects of Aloe vera on Burn Injuries: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. J Burn Care Res. 2024;45:153645. [DOI] [PubMed]
Drudi D, Tinto D, Ferranti D, Fiorelli F, Pozzo MD, Capitani O. Aloe barbadensis miller versus silver sulfadiazine creams for wound healing by secondary intention in dogs and cats: A randomized controlled study. Res Vet Sci. 2018;117:19. [DOI] [PubMed]
Goudarzi M, Fazeli M, Azad M, Seyedjavadi SS, Mousavi R. Aloe vera Gel: Effective Therapeutic Agent against Multidrug-Resistant Pseudomonas aeruginosa Isolates Recovered from Burn Wound Infections. Chemother Res Pract. 2015;2015:639806. [DOI] [PubMed] [PMC]
Fani M, Kohanteb J. Inhibitory activity of Aloe vera gel on some clinically isolated cariogenic and periodontopathic bacteria. J Oral Sci. 2012;54:1521. [DOI] [PubMed]
Molla MTH, Ahsan MS, Alam MT, Haque ME. Antibacterial activity in the leaves of seven bitter medicinal plants of Bangladesh. J Bio Sci. 2010;18:12833. [DOI]
Giostri GS, Novak EM, Buzzi M, Guarita-Souza LC. Treatment of acute wounds in hand with Calendula officinalis L.: A randomized trial. Tissue Barriers. 2022;10:1994822. [DOI] [PubMed] [PMC]
Rezai S, Rahzani K, Hekmatpou D, Rostami A. Effect of oral Calendula officinalis on second-degree burn wound healing. Scars Burn Heal. 2023;9:20595131221134053. [DOI] [PubMed] [PMC]
Shankar SM, Bardvalli SG, Jyotirmayee R, Chethana, Bhushan K, Kumar S. Efficacy of Calendula officinalis extract (marigold flower) as an antimicrobial agent against oral microbes: an in vitro study in comparison with chlorhexidine digluconate. J Clin Diagn Res. 2017;11:ZC0510. [DOI]
Larçin Ö, Körpe DA, İşeri ÖD, Şahin Fİ. Phenolic composition and antibacterial activity of crude methanolic Calendula officinalis flower extract against plant pathogenic bacteria. Eur J Biol. 2015;74:2533.
Araújo LU, Reis PG, Barbosa LC, Saúde-Guimarães DA, Grabe-Guimarães A, Mosqueira VC, et al. In vivo wound healing effects of Symphytum officinale L. leaves extract in different topical formulations. Pharmazie. 2012;67:35560. [PubMed]
Yakan S, Dağlıoğlu YK, Erdoğan KE, Sağlamtaş R, Gülçin İ. Antioxidant and wound healing effects of comfrey (Symphytum officinale). Rev Cient Fac Vet. 2025;35:18. [DOI]
Barna M, Kucera A, Hladícova M, Kucera M. Wound healing effects of a Symphytum herb extract cream (Symphytum x uplandicum NYMAN: ): results of a randomized, controlled double-blind study. Wien Med Wochenschr. 2007;157:56974. [DOI] [PubMed]
Mârza SM, Dăescu AM, Purdoiu RC, Dragomir M, Tătaru M, Melega I, et al. Healing of Skin Wounds in Rats Using Creams Based on Symphytum Officinale Extract. Int J Mol Sci. 2024;25:3099. [DOI] [PubMed] [PMC]
Thibane VS, Ndhlala AR, Abdelgadir HA, Finnie JF, Van Staden J. The cosmetic potential of plants from the Eastern Cape Province traditionally used for skincare and beauty. S Afr J Bot. 2019;122:47583. [DOI]
Bouzada MLM, Fabri RL, Nogueira M, Konno TUP, Duarte GG, Scio E. Antibacterial, cytotoxic and phytochemical screening of some traditional medicinal plants in Brazil. Pharm Biol. 2009;47:4452. [DOI]
de Moura FBR, Ferreira BA, Deconte SR, Landim BC, Justino AB, Aro AA, et al. Wound healing activity of the hydroethanolic extract of the leaves of Maytenus ilicifolia Mart. Ex Reis. J Tradit Complement Med. 2021;11:44656. [DOI] [PubMed] [PMC]
Lima AP, Leite NS, Camargo EA, Estevam CS, Pantaleão SM, Fernandes RPM, et al. Avaliação da atividade cicatrizante do extrato etanólico da casca de Maytenus rigida Mart. (Celastraceae). Sci Plena. 2010;6.
Oliveira JFS, de Assis Bastos ML, Santos RCS, Junior S, Junior PFDSS, Araújo MV, et al. Phytochemical profile and evaluation of antibacterial and cytotoxic activity of Maytenus rigida (Mart.) extracts and fractions. J Chem Pharm Res. 2016;8:74651.
Castelo Branco Rangel de Almeida Cde F, de Vasconcelos Cabral DL, Rangel de Almeida CC, Cavalcanti de Amorim EL, de Araújo JM, de Albuquerque UP. Comparative study of the antimicrobial activity of native and exotic plants from the Caatinga and Atlantic Forest selected through an ethnobotanical survey. Pharm Biol. 2012;50:2017. [DOI] [PubMed]
Cavalcanti JM, Leal-Cardoso JH, Diniz LR, Portella VG, Costa CO, Linard CF, et al. The essential oil of Croton zehntneri and trans-anethole improves cutaneous wound healing. J Ethnopharmacol. 2012;144:2407. [DOI] [PubMed]
Casao TDRL, Pinheiro CG, Sarandy MM, Zanatta AC, Vilegas W, Novaes RD, et al. Croton urucurana Baillon stem bark ointment accelerates the closure of cutaneous wounds in knockout IL-10 mice. J Ethnopharmacol. 2020;261:113042. [DOI] [PubMed]
de Sousa Machado LC, Pfrimer IAH, Magalhães MR. Cicatrização de feridas induzidas por peçonha de Bothrops moojeni pelo extrato de Croton urucurana. Rev Estud Ciênc Ambient Saúde. 2015;42:597611. [DOI]
Araujo FM, Dantas MC, e Silva LS, Aona LY, Tavares IF, de Souza-Neta LC. Antibacterial activity and chemical composition of the essential oil of Croton heliotropiifolius Kunth from Amargosa, Bahia, Brazil. Ind Crops Prod. 2017;105:2036. [DOI]
da Costa JG, Campos AR, Brito SA, Pereira CK, Souza EO, Rodrigues FF. Biological screening of araripe basin medicinal plants using Artemia salina Leach and pathogenic bacteria. Pharmacogn Mag. 2010;6:3314. [DOI] [PubMed] [PMC]
Andrade TC, De Lima SG, Freitas RM, Rocha MS, Islam T, Da Silva TG, et al. Isolation, characterization and evaluation of antimicrobial and cytotoxic activity of estragole, obtained from the essential oil of Croton zehntneri (Euphorbiaceae). An Acad Bras Cienc. 2015;87:17382. [DOI] [PubMed]
Oliveira IS, Lima JCS, Silva RM, Martins DT. Triagem da atividade antibacteriana in vitro do látex e extratos de Croton urucurana Baill. Rev Bras Farmacogn. 2008;18:58793. Portuguese. [DOI]
Nader TT, Coppede JS, Taleb-Contini SH, Amaral LA, Pereira AMS. Atividade antibiofilme de substâncias de Croton urucurana em Staphylococcus aureus isolado de mastite bovina. Pesq Vet Bras. 2018;38:17139. [DOI]
de Santana Neres W, Aragão JMDA, Nascimento ACS, Santos JF, Matos SS, de Souza DA, et al. The enhanced healing effect of Anadenanthera colubrina ethanolic extract on excisional skin wounds in mice. Research Article [Preprint]. 2024 [cited 2025 Nov 20]. Available from: https://doi.org/10.21203/rs.3.rs-5326954/v1
Pessoa WS, Estevão LR, Simões RS, Barros ME, Mendonça Fde S, Baratella-Evêncio L, et al. Effects of angico extract (Anadenanthera colubrina var. cebil) in cutaneous wound healing in rats. Acta Cir Bras. 2012;27:65570. [DOI] [PubMed]
Rodrigo Cavalcante de Araújo D, Diego da Silva T, Harand W, Sampaio de Andrade Lima C, Paulo Ferreira Neto J, de Azevedo Ramos B, et al. Bioguided Purification of Active Compounds from Leaves of Anadenanthera colubrina var. cebil (Griseb.) Altschul. Biomolecules. 2019;9:590. [DOI] [PubMed] [PMC]
Das Chagas Almeida A, Azevedo Rodrigues L, Dos Santos Paulino G, Pereira Aguilar A, Andrade Almeida A, Olavo Ferreira S, et al. Prenylated flavonoid-enriched fraction from Maclura tinctoria shows biological activity against Staphylococcus aureus and protects Galleria mellonella larvae from bacterial infection. BMC Complement Altern Med. 2019;19:189. [DOI] [PubMed] [PMC]
Kobayashi YT da S, Almeida VT de, Bandeira T, Alcântara BN de, Silva ASB da, Barbosa WLR, et al. Phytochemical evaluation and wound healing potential of the fruit extract ethanolic of Libidibia ferrea (Mart. ex Tul.) L.P. Queiroz in Wistar rats. Braz J Vet Res Anim Sci. 2015;52:3440. [DOI]
Batista EKF, Trindade HID, Farias IDS, Martins FMM, Silva Filho OFD, Batista MDCDS. Avaliação da atividade cicatrizante de preparados à base de jucá (Caesalpinia ferrea Mart.). Braz J Vet Res Anim Sci. 2017;54:21522.
de Medeiros Oliveira IVP, da Cunha Dias RV, Calado EB, de Lucena BBM, da Costa ALF, Sakamoto SM. Avaliação cicatricial macroscópica da vagem e da casca do jucá (Caesalpinia ferrea Mart. ex Tul. var. ferrea) em lesões cutâneas em asininos (Equus asinus). Acta Vet Bras. 2014;8:12935.
Mota MRL, do Carmo Filho JRL, Martins TV, Soares DQ, de Sousa MP, de Barros Silva PG, et al. Polysaccharide extract of Caesalpinia ferrea (Mart) pods attenuates inflammation and enhances the proliferative phase of rat cutaneous wounds. Inflammopharmacology. 2022;30:1799810. [DOI] [PubMed]
Pereira Lde P, Mota MR, Brizeno LA, Nogueira FC, Ferreira EG, Pereira MG, et al. Modulator effect of a polysaccharide-rich extract from Caesalpinia ferrea stem barks in rat cutaneous wound healing: Role of TNF-α, IL-1β, NO, TGF-β. J Ethnopharmacol. 2016;187:21323. [DOI] [PubMed]
Veloso DJ, Abrão F, Martins CHG, Bronzato JD, Gomes BPFA, Higino JS, et al. Potential antibacterial and anti-halitosis activity of medicinal plants against oral bacteria. Arch Oral Biol. 2020;110:104585. [DOI] [PubMed]
Nascimento PLA, Nascimento TCES, Gomes JEG, Silva MDS, Souza SA, Silva TM, et al. Antioxidant and antimicrobial properties of ethanolic extract of Libidibia ferrea pods. Rev Fitos. 2015;9:20716.
Sampaio FC, Pereira Mdo S, Dias CS, Costa VC, Conde NC, Buzalaf MA. In vitro antimicrobial activity of Caesalpinia ferrea Martius fruits against oral pathogens. J Ethnopharmacol. 2009;124:28994. [DOI] [PubMed]
Paiva LA, de Alencar Cunha KM, Santos FA, Gramosa NV, Silveira ER, Rao VS. Investigation on the wound healing activity of oleo-resin from Copaifera langsdorffi in rats. Phytother Res. 2002;16:7379. [DOI] [PubMed]
Gushiken LFS, Hussni CA, Bastos JK, Rozza AL, Beserra FP, Vieira AJ, et al. Skin Wound Healing Potential and Mechanisms of the Hydroalcoholic Extract of Leaves and Oleoresin of Copaifera langsdorffii Desf. Kuntze in Rats. Evid Based Complement Alternat Med. 2017;2017:6589270. [DOI] [PubMed] [PMC]
Kauer DP, de Moura Alonso J, Gushiken LFS, Lemos M, Padovani CR, Rodrigues CA, et al. Experimental skin wound treatment with Copaifera langsdorffii Desf. Kuntze (Leguminosae) extract and oil-resin in horses. Braz J Vet Res Anim Sci. 2020;57(3):e166095. [DOI]
de Oliveira Souza É, Cominote M, Barreto JG, Krause KB, Pimentel-Schmitt EF, Fronza M, et al. Wound healing effects of Copaifera sp. essential oils and Cyrtopodium flavum ethanolic extracts. InterSciencePlace. 2022;17(3).
Martini CA, Scapini JG, Collaço LM, Matsubara A, Veiga Júnior VF. Comparative analysis of the effects of Copaifera multijuga oil-resin and nitrofurazona in the cutaneous wound healing process. Rev Col Bras Cir. 2016;43:44551. [DOI] [PubMed]
Cardinelli CC, Passos JTG, Veiga-Junior VF, de Oliveira BGRB, Santos EPD, Neto GG, et al. Skin Tear Treatment with Copaifera multijuga Hayne in Polymeric Hydrogel: A Randomized Clinical Trial. Pharmaceuticals (Basel). 2024;17:1691. [DOI] [PubMed] [PMC]
Ribeiro VP, Arruda C, da Silva JJM, Aldana Mejia JA, Furtado NAJC, Bastos JK. Use of spinning band distillation equipment for fractionation of volatile compounds of Copaifera oleoresins for developing a validated gas chromatographic method and evaluating antimicrobial activity. Biomed Chromatogr. 2019;33(2):e4412. [DOI]
Masson DS, Salvador SLDS, Polizello ACM, Frade MAC. Atividade antimicrobiana do óleo-resina de copaíba (Copaifera langsdorffii) em bactérias de significância clínica em úlceras cutâneas. Rev Bras Plantas Med. 2013;15:6649.
de Lucena CCO, da Silva CJA, Mendes RFV, de Sena KXFR, da Silva TG, Ximenes RM. Phytochemical screening and biological activities of Copaifera langsdorffii Desf. (Fabaceae) organic extracts. J Med Plants Res. 2024;18:2235. [DOI]
Alves JA, Abrão F, da Silva Moraes T, Damasceno JL, Dos Santos Moraes MF, Sola Veneziani RC, et al. Investigation of Copaifera genus as a new source of antimycobaterial agents. Future Sci OA. 2020;6:FSO587. [DOI] [PubMed] [PMC]
Silva AN, Soares ACF, Cabral MM, Andrade ARD, Silva MBD, Martins CH, et al. Antitubercular activity increase in labdane diterpenes from Copaifera oleoresin through structural modification. J Braz Chem Soc. 2017;28:110612. [DOI]
Abrão F, de Araújo Costa LD, Alves JM, Senedese JM, de Castro PT, Ambrósio SR, et al. Copaifera langsdorffii oleoresin and its isolated compounds: antibacterial effect and antiproliferative activity in cancer cell lines. BMC Complement Altern Med. 2015;15:443. [DOI] [PubMed] [PMC]
Souza AB, de Souza MG, Moreira MA, Moreira MR, Furtado NA, Martins CH, et al. Antimicrobial evaluation of diterpenes from Copaifera langsdorffii oleoresin against periodontal anaerobic bacteria. Molecules. 2011;16:96119. [DOI] [PubMed] [PMC]
da Costa RSL, Martins DS, Peixoto LDC, da Silva BJP, Borges LB, Lima ES, et al. Antioxidant effect of Hymenaea courbaril L. sap on the healing of wounds on mice. J Med Plants Res. 2021;15:16071. [DOI]
de Andrade FM, Neves FPA, de Albuquerque PBS, Aragão-Neto AC, Jandú JJB, Coelho LCBB, et al. Healing activities of Cramoll and xyloglucan membrane in cutaneous wounds of diabetic mice. J Immunol Regen Med. 2021;13:100045. [DOI]
de Sales Diodato J, da Costa Silva JT, Weverton Almeida-Bezerra J, Felipe Felício M, Fernandes Teixeira G, Santos da Silva LY, et al. In vitro evaluation of the antimicrobial potential of extracts of Hymenaea courbaril L. (Fabaceae). Rev Gest Soc Ambient. 2025;19. [DOI]
Núñez MJ, Paz-González AD, Vázquez-Jiménez LK, Castillo UG, Moo-Puc R, Chan-Bacab JM, et al. In vitro antiparasitic and antibacterial evaluation of organic extracts of Salvadoran flora. Bol Latinoam Caribe Plantas Med Aromat. 2023;22:1936. [DOI]
Everton GO, Pereira PM, Rosa VS, Mafra NSC, Santos Júnior PS, Souza FS, et al. Chemical characterization, toxicity, antioxidant and antimicrobial activity of the essential oils of Hymenaea courbaril L. and Syzygium cumini (L.) Skeels. Cienc Nat. 2021;43. [DOI]
Martins CHG, Souza FR, Fonseca C, Casemiro LA, Furtado NAJC, Ambrósio SR, Cunha WR. Determinação in vitro da atividade antibacteriana dos extratos brutos da casca e polpa farinácea de Hymenaea courbaril L. Investigação. 2010;10:3743.
Santos AT, Maurício Júnior J, Cunha GN. Cicatrização por segunda intenção de feridas cutâneas em ratos Wistar com uso de Stryphnodendron adstringens. Ciênc Anim (Impr.). 2019:1529.
de Souza de Aguiar P, Correa ÁP, Antunes FTT, de Barros Ferraz AF, Vencato SB, Amado GJV, et al. Benefits of Stryphnodendron adstringens when associated with hydrogel on wound healing in diabetic rats. Clin Phytosci. 2021;7:22. [DOI]
Pinto SC, Bueno FG, Panizzon GP, Morais G, Dos Santos PV, Baesso ML, et al. Stryphnodendron adstringens: Clarifying Wound Healing in Streptozotocin-Induced Diabetic Rats. Planta Med. 2015;81:10906. [DOI] [PubMed]
Hernandes L, da Silva Pereira LM, Palazzo F, de Mello JCP. Wound-healing evaluation of ointment from Stryphnodendron adstringens (barbatimão) in rat skin. Braz J Pharm Sci. 2010;46:4316. [DOI]
Martins KLE, Lima VCN, Biancardi MF, Galdino Júnior H, Vinaud MC, de Souza Lino Júnior R. Effects of Fitoscar™ (dry extract of Stryphnodendron adstringens 50%) on the healing of acute wounds in Wistar rats. Contrib Cienc Soc. 2024;17:e7657. [DOI]
Santos VR, Gomes RT, Oliveira RR, Cortés ME, Brandão MGL. Susceptibility of oral pathogenic microorganisms to aqueous and ethanolic extracts of Stryphnodendron adstringens (barbatimão). Int J Dent. 2009;8:15.
da Cruz JER, Costa JLG, Teixeira TA, Oliveira e Freitas GR, de Souza Gomes M, Morais ER. Phenolic compounds, antioxidant and antibacterial activity of extract from leaves and bark of Stryphnodendron adstringens (Mart.) Coville. Rev Cienc Agron. 2022;53:e20217903. [DOI]
Santos JPCL. Potencial antimicrobiano do extrato etanólico da casca de Stryphnodendron barbatimam (Mart.) ante microrganismos de interesse médico-odontológico. RSBO. 2021;18:2330.
Trevisan DAC, Batista AFP, Campanerut-Sá PAZ, de Medeiros Araújo DC, Ribeiro TDVR, de Medeiros Araújo DC, et al. Synergistic activity of Stryphnodendron adstringens and potassium sorbate against foodborne bacteria. Arch Microbiol. 2022;204:292. [DOI] [PubMed]
Pawar RS, Kumar S, Toppo FA, PK L, Suryavanshi P. Sida cordifolia Linn. accelerates wound healing process in type 2 diabetic rats. J Acute Med. 2016;6:829. [DOI]
Pawar RS, Chaurasiya PK, Rajak H, Singour PK, Toppo FA, Jain A. Wound healing activity of Sida cordifolia Linn. in rats. Indian J Pharmacol. 2013;45:4748. [DOI] [PubMed] [PMC]
Francis P, Masimba PJ, Mwakigonja AR. Evaluation of the wound healing activity of formulated ointments and water preparation from Sida rhombifolia leaf extract. Tanzan J Health Res. 2018;20. [DOI]
Halilu ME, Muhammad I, Dangoggo SM, Farouq AA, Ahmed A, Shamsuddeen AA, et al. Phytochemical and antibacterial screening of petroleum ether and ethanol extracts of Sida cordifolia leaves. J Chem Soc Niger. 2016;41.
Ahirrao P, Tambat R, Kamboj A, Jain UK, Nandanwar HS. Modulation activity of Sida cordifolia L. and Sida rhombifolia L. in Staphylococcus aureus SA-1199B. Int Res J Pharm. 2019;10:11521.
Assam AJ, Dzoyem JP, Pieme CA, Penlap VB. In vitro antibacterial activity and acute toxicity studies of aqueous-methanol extract of Sida rhombifolia Linn. (Malvaceae). BMC Complement Altern Med. 2010;10:40. [DOI] [PubMed] [PMC]
Salunke MR, Shinde V. Molecular insights and efficacy of guava leaf oil emulgel in managing non diabetic as well as diabetic wound healing by reducing inflammation and oxidative stress. Inflammopharmacology. 2025;33:1491503. [DOI] [PubMed]
Bilal K, Mehboob F, Akhtar N, Mirza IA, Okla MK, Dar MJ, et al. Wound healing, antioxidant and antibacterial activities of polyphenols of Psidium guajava L. leaves. S Afr J Bot. 2024;165:53851. [DOI]
Change for: Bilal K, Mehboob F, Akhtar N, Mirza IA, Okla MK, Dar MJ, et al. Wound healing, antioxidant and antibacterial activities of polyphenols of Psidium guajava L. leaves. S Afr J Bot. 2024;165:538-51.https://doi.org/10.1016/j.sajb.2023.12.026Samuvel RMS, Mahendran S, Muralidharan K, Swain D, Ramalingam V. Phytometabolome of Psidium guajava inhibits biofilm formation of Escherichia coli and augmented acute wound repair. Biocatal Agric Biotechnol. 2024;58:103175. [DOI]
Uchôa VT, Da Palma AF, Marques LK, Carneiro RD, Sousa GF, Ferreira DC, et al. Avaliação dos extratos hidroalcoólicos do caule e folhas da Ximenia americana L. na cicatrização de feridas excisionais agudas em pele de camundongos. Rev Virtual Quim. 2020;12:3750.
Souza Neto Júnior JC, Estevão LRM, Ferraz AA, Simões RS, Vieira MGF, Evêncio-Neto J. Ointment of Ximenes americana promotes acceleration of wound healing in rats1. Acta Cir Bras. 2019;34:e201900307. [DOI] [PubMed] [PMC]
Kiessoun K, Roland MNT, Mamounata D, Yomalan K, Sytar O, Souz A, et al. Antimicrobial profiles, antidiarrheal and antipyretic capacities of phenol acid rich-fractions from Ximenia americana L. (Olacaceae) in Wistar albino rats. Int J Pharm Pharm Sci. 2018;10:628.
Ballo M, Somboro AM, Maiga M, Diarra B, Sanogo M, Denou A, et al. Evaluation of antimycobacterial activity of medicinal plants used by Malian traditional medicine practitioners to treat tuberculosis. Int J Biol Chem Sci. 2020;14:314555. [DOI]
Sartika D, Afrianti R, Aisy R, Rahmi M. Effectiveness of the ointment of forest betel leaves extract (Piper aduncum L.) against excision wounds. Jurnal Katalisator. 2024;9:12131. [DOI]
Morais VP, Fernandes CC, Martins CHG, Crotti AEM, Miranda MLD. Bioactive hexane extracts from Piper aduncum and Xylopia aromatica against bacterial strains which cause food poisoning. Rev Virtual Quim. 2023;15. [DOI]
Magalhães CF, de Siqueira EP, de Oliveira EA, Zani CL, Peres RL, dos Santos KA, et al. Antimicrobial activity of Piper aduncum leaf extracts against the dental plaque bacteria Streptococcus mutans and Streptococcus sanguinis. J Med Plants Res. 2016;10:3317. [DOI]
da Silva ACA, Matias EFF, Rocha JE, Araújo ACJ, de Freitas TS, Campina FF, et al. Gas chromatography coupled to mass spectrometry (GC-MS) characterization and evaluation of antibacterial bioactivities of the essential oils from Piper arboreum Aubl., Piper aduncum L. e Piper gaudichaudianum Kunth. Z Naturforsch C J Biosci. 2020;76:3542. [DOI] [PubMed]
Dos Santos VLP, Ribas JLC, de Lima CP, Campos R, Garcia AC, Budel JM, et al. The wound healing effect of aqueous extract from Piper amalago L. in diabetic patient. Explore (NY). 2020;16:36871. [DOI] [PubMed]
Menon DN, Leite IAB, Ramsdorf MTA, Chagas LDS, Arroyo SA, Santos ACD, et al. Effect of ethanolic extracts from Piperaceae leaves on the reduction of skin necrosis and wound healing in an animal model of degloving injuries. Acta Cir Bras. 2023;38:e387223. [DOI] [PubMed] [PMC]
Ruiz SP, Anjos MM, Carrara VS, Delima JN, Cortez DA, Nakamura TU, et al. Evaluation of the antibacterial activity of Piperaceae extracts and nisin on Alicyclobacillus acidoterrestris. J Food Sci. 2013;78:M17727. [DOI] [PubMed]
Setzer WN, Park G, Agius BR, Stokes SL, Walker TM, Haber WA. Chemical compositions and biological activities of leaf essential oils of twelve species of Piper from Monteverde, Costa Rica. Nat Prod Commun. 2008;3:1934578X0800300823. [DOI]
Soares KD, Bordignon SAL, Apel MA. Chemical composition and anti-inflammatory activity of the essential oils of Piper gaudichaudianum and Piper mikanianum. J Ethnopharmacol. 2022;297:115533. [DOI] [PubMed]
Leal ALAB, da Silva MC, Silva AKFE, de Souza Mesquita AB, Bezerra CF, Dotto ARF, et al. Chemical composition of Piper gaudichaudianum Kunth essential oil and evaluation of its antimicrobial and modulatory effects on antibiotic resistance, antibiofilm, and cell dimorphism inhibitory activities. 3 Biotech. 2023;13:255. [DOI] [PubMed] [PMC]
Silva ACA, Diodato JS, Castro JW, Matias EFF, Silva LE, do Amaral W, et al. Effect of the essential oils from Piper sp. and blue LED lights in the enhancement of the antibiotic activity of drugs against MDR bacterial strains. J Photochem Photobiol B. 2019;199:111604. [DOI]
Ribeiro BIO, Pascoli IC, Castro JC, dos Anjos Szczerepa MM, Dias Filho BP, Nakamura CV, et al. Antimicrobial activity of extracts of Piper peltatum and Piper marginatum on Klebsiella spp., Staphylococcus aureus, Salmonella spp., Escherichia coli and Bacillus subtilis. Rev Bras Plantas Med. 2020;22:14549. [DOI]
de Pascoli IC, dos Anjos MM, da Silva AA, Lorenzetti FB, Cortez DAG, Mikcha JMG, et al. Piperaceae extracts for controlling Alicyclobacillus acidoterrestris growth in commercial orange juice. Ind Crops Prod. 2018;116:22430.
de Silva Junior IF, Balogun SO, de Oliveira RG, Damazo AS, Martins DTO. Piper umbellatum L.: A medicinal plant with gastric-ulcer protective and ulcer healing effects in experimental rodent models. J Ethnopharmacol. 2016;192:12331. [DOI] [PubMed]
Werka JS, Boehme AK, Setzer WN. Biological activities of essential oils from Monteverde, Costa Rica. Nat Prod Commun. 2007;2:1934578X0700201204. [DOI]
Isobe T, Ohsaki A, Nagata K. Antibacterial constituents against Helicobacter pylori of Brazilian medicinal plant, Pariparoba. Yakugaku Zasshi. 2002;122:2914. Japanese. [DOI] [PubMed]
Ghanadian M, Soltani R, Homayouni A, Khorvash F, Jouabadi SM, Abdollahzadeh M. The Effect of Plantago major Hydroalcoholic Extract on the Healing of Diabetic Foot and Pressure Ulcers: A Randomized Open-Label Controlled Clinical Trial. Int J Low Extrem Wounds. 2024;23:47581. [DOI] [PubMed] [PMC]
Keshavarzi A, Montaseri H, Akrami R, Moradi Sarvestani H, Khosravi F, Foolad S, et al. Therapeutic Efficacy of Great Plantain (Plantago major L.) in the Treatment of Second-Degree Burn Wounds: A Case-Control Study. Int J Clin Pract. 2022;2022:4923277. [DOI] [PubMed] [PMC]
Pachla A, da Cruz FSF, de Fátima Colet C. Efeito cicatrizante do extrato de Plantago tomentosa em cadelas submetidas a ovariohisterectomia. Semina Cienc Biol Saude. 2017;38:13744. [DOI]
Bouali A, Spissu Y, Barberis A, Fadda A, Azara E, Orrù G, et al. Phytochemical evaluation and exploration of some biological activities of aqueous and ethanolic extracts of two species of the genus Plantago L. PLoS One. 2024;19:e0298518. [DOI] [PubMed] [PMC]
Silva-Correa CR, Rosas-Cruz GP, Calderón-Peña AA, Torre VEV, Aspajo-Villalaz CL, Castañeda-Carranza JA, et al. Effects of Solanum tuberosum L. ointment on second-degree burns in mice. Vet World. 2023;16:24405. [DOI] [PubMed] [PMC]
Rosas-Cruz GP, Silva-Correa CR, Calderón-Peña AA, Villarreal-La Torre VE, Aspajo-Villalaz CL, Cruzado-Razco JL, et al. Wound healing activity of an ointment from Solanum tuberosum L. “Tumbay yellow potato” on Mus musculus BALB/c. Pharmacogn J. 2020;12:126875. [DOI]
Subrahmanyam M. Honey dressing versus boiled potato peel in the treatment of burns: a prospective randomized study. Burns. 1996;22:4913. [DOI] [PubMed]
Dattatreya RM, Nuijen S, van Swaaij AC, Klopper PJ. Evaluation of boiled potato peel as a wound dressing. Burns. 1991;17:3238. [DOI] [PubMed]
Fertilita S, Zulfadli M, Larasati V, Rasyid RSP, Argentina F, Tanta Y, et al. Effectiveness of cherry tomato extract in gel form to accelerate the healing process of excision wounds in Wistar white rats. Biol Med Nat Prod Chem. 2025;14:42734. [DOI]
Sánchez LM, Bulnes C, Pérez P, Rodríguez A, Noa M, Ginorio C, et al. Actividad antibacteriana, cicatrizante y útero-estimulante de Solanum americanum Miller. Actual Biol. 2003;25:18. [DOI]
Maz’uma A, Dadah AJ, Uba A. Antibacterial activity of Citrus sinensis and Solanum lycopersicum on wounds isolated from hospitals in Kaduna metropolis, Nigeria. Int J Biomed Mater Res. 2018;6:409. [DOI]
Edziri H, Ammar S, Souad L, Mahjoub MA, Mastouri M, Aouni M, et al. In vitro evaluation of antimicrobial and antioxidant activities of some Tunisian vegetables. S Afr J Bot. 2012;78:2526.
Bontempo P, Carafa V, Grassi R, Basile A, Tenore GC, Formisano C, et al. Antioxidant, antimicrobial and anti-proliferative activities of Solanum tuberosum L. var. Vitelotte. Food Chem Toxicol. 2013;55:30412. [DOI] [PubMed]
Whittemore R, Knafl K. The integrative review: updated methodology. J Adv Nurs. 2005;52:54653. [DOI] [PubMed]
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Cota BB. Medicinal plants for skin and wound-healing in Brazil: an ethnobotanical and antibacterial review. Explor Drug Sci. 2026;4:1008164. https://doi.org/10.37349/eds.2026.1008164
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