Evidence map›Paper›PMID 41196291›Full record

ArticleEuropean journal of microbiology & immunology2025

Topical microemulsion with phenolic compounds from Libidibia ferrea (Fabaceae): An alternative treatment for cutaneous leishmaniasis.

Bruno Bezerra Jensen, Katia Solange Cardoso Rodrigues Dos Santos, Claudia Dantas Comandolli-Wyrepkowski, Felipe Moura Araujo da Silva, Caio Coutinho de Souza, Maria da Paz Lima, José Fernando Marques Barcellos, Tatiane Pereira de Souza, Fabrício Nonato Araújo Rolim, Francimeire Gomes Pinheiro and 1 more

Abstract read
In one paragraph

Article in European journal of microbiology & immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Bruno Bezerra Jensen1Postgraduate Program in Pharmaceutical Innovation, Faculty of Pharmaceutical Sciences, Federal University of Amazonas (UFAM), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0002-9102-9698
Katia Solange Cardoso Rodrigues Dos Santos1Postgraduate Program in Pharmaceutical Innovation, Faculty of Pharmaceutical Sciences, Federal University of Amazonas (UFAM), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0002-1054-2853
Claudia Dantas Comandolli-Wyrepkowski2Laboratory of Leishmaniasis and Chagas Disease, National Institute for Amazonian Research (INPA), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0001-9699-7308
Felipe Moura Araujo da Silva3Multidisciplinary Support Center, Federal University of Amazonas (UFAM), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0002-1809-1372
Caio Coutinho de Souza2Laboratory of Leishmaniasis and Chagas Disease, National Institute for Amazonian Research (INPA), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0002-5107-8727
Maria da Paz Lima4Coordination for Technology and Innovation, National Institute for Amazonian Research (INPA), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0002-0255-0693
José Fernando Marques Barcellos5Department of Morphology, Institute of Biological Sciences, Federal University of Amazonas (UFAM), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0003-2149-7899
Tatiane Pereira de Souza1Postgraduate Program in Pharmaceutical Innovation, Faculty of Pharmaceutical Sciences, Federal University of Amazonas (UFAM), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0003-1164-2191
Fabrício Nonato Araújo Rolim1Postgraduate Program in Pharmaceutical Innovation, Faculty of Pharmaceutical Sciences, Federal University of Amazonas (UFAM), Manaus, Amazonas, Brazil.
Francimeire Gomes Pinheiro2Laboratory of Leishmaniasis and Chagas Disease, National Institute for Amazonian Research (INPA), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0002-8897-6088
Antonia Maria Ramos Franco1Postgraduate Program in Pharmaceutical Innovation, Faculty of Pharmaceutical Sciences, Federal University of Amazonas (UFAM), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0000-0002-4300-5325

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The pharmacotherapy of cutaneous leishmaniasis is invasive and presents several adverse reactions, which reinforces the need for topical and less toxic alternatives. Methods: Topical microemulsions containing phenolic compounds from Libidibia ferrea (Fabaceae) were developed, physicochemically characterized, and tested in hamsters (Mesocricetus auratus) experimentally infected with Leishmania amazonensis. After treatment, clinical progression of lesions, histopathological alterations, and parasite load were evaluated. The dichloromethane (DCM) fraction of the extract was analyzed by mass spectrometry, and the main compounds were isolated. Results: The optimized microemulsion effectively controlled lesion progression, showing only a 25% increase in lesion volume, compared to a 383% increase for the group without treatment, and presented a moderate inflammatory response. A new phenolic compound, named libidine (phenylpropanoic acid derivative), along with methyl gallate, was isolated from the DCM fraction. Conclusions: The topical formulation was as effective as Glucantime® (antimonial standard treatment) and produced a significant reduction in parasite load, consistent with the antileishmanial activity previously reported for phenolic acids and their derivatives.

Indexed as

Leishmania amazonensisLibidibia ferreamicroemulsion systemorganic acid derivativestopical treatment

Identifiers

PMID41196291
PMCPMC12771332

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.