European journal of microbiology & immunology · 2025
Topical microemulsion with phenolic compounds from Libidibia ferrea (Fabaceae): An alternative treatment for cutaneous leishmaniasis.
СтатьяНазвание и аннотация: Перевод в очереди
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Jensen Bruno Bezerra, Cardoso Rodrigues Dos Santos Katia Solange, Comandolli-Wyrepkowski Claudia Dantas, Araujo da Silva Felipe Moura, Coutinho de Souza Caio, da Paz Lima Maria, Marques Barcellos José Fernando, Pereira de Souza Tatiane, Araújo Rolim Fabrício Nonato, Pinheiro Francimeire Gomes, Ramos Franco Antonia Maria
Аннотация
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.
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.