Back to Search
Start Over
Microemulsions strongly promoted the activity of α-bisabolol against different Leishmania species and its skin permeation.
- Source :
-
Experimental parasitology [Exp Parasitol] 2024 Oct; Vol. 265, pp. 108808. Date of Electronic Publication: 2024 Jul 31. - Publication Year :
- 2024
-
Abstract
- This study aimed to develop microemulsions (MEs) containing α-bisabolol for the topical treatment of cutaneous leishmaniasis (CL). Initially, pseudoternary phase diagrams were developed using α-bisabolol as the oil phase, Eumulgin® CO 40 as the surfactant, Polymol® HE as the co-surfactant, and distilled water as the aqueous phase. Two transparent liquid systems (TLS) containing 5% of α-bisabolol were selected and characterized (F5E25 and F5EP25). Next, skin permeation and retention assays were performed using Franz cells. The interaction of the formulation with the stratum corneum (SC) was evaluated using the FTIR technique. The cytotoxicity was evaluated in murine peritoneal macrophages. Finally, the antileishmanial activity of microemulsions was determined in promastigotes and amastigotes of L. amazonensis (strain MHOM/BR/77/LTB 0016). As a result, the selected formulations showed isotropy, nanometric size (below 25 nm), Newtonian behavior and pH ranging from 6.5 to 6.9. The MEs achieved a 2.5-fold increase in the flux and skin-permeated amount of α-bisabolol. ATR-FTIR results showed that microemulsions promoted fluidization and extraction of lipids and proteins of the stratum corneum, increasing the diffusion coefficient and partition coefficient of the drug in the skin. Additionally, F5E25 and F5EP25 showed higher activity against promastigotes (IC <subscript>50</subscript> 13.27 and 18.29, respectively) compared to unencapsulated α-bisabolol (IC <subscript>50</subscript> 53.8). Furthermore, F5E25 and F5EP25 also showed antileishmanial activity against intracellular amastigotes of L. amazonensis, with IC <subscript>50</subscript> 50 times lower than free α-bisabolol and high selectivity index (up to 15). Therefore, the systems obtained are favorable to topical administration, with significant antileishmanial activity against L. amazonensis promastigotes and amastigotes, being a promising system for future in vivo trials.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Mice
Leishmaniasis, Cutaneous drug therapy
Leishmaniasis, Cutaneous parasitology
Spectroscopy, Fourier Transform Infrared
Skin Absorption drug effects
Mice, Inbred BALB C
Female
Leishmania drug effects
Surface-Active Agents pharmacology
Surface-Active Agents chemistry
Antiprotozoal Agents pharmacology
Antiprotozoal Agents chemistry
Monocyclic Sesquiterpenes pharmacology
Monocyclic Sesquiterpenes chemistry
Emulsions chemistry
Sesquiterpenes pharmacology
Sesquiterpenes chemistry
Skin parasitology
Macrophages, Peritoneal drug effects
Macrophages, Peritoneal parasitology
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2449
- Volume :
- 265
- Database :
- MEDLINE
- Journal :
- Experimental parasitology
- Publication Type :
- Academic Journal
- Accession number :
- 39094996
- Full Text :
- https://doi.org/10.1016/j.exppara.2024.108808