Development, characterization, and anti-leishmanial activity of topical amphotericin B nanoemulsions.

Drug Deliv Transl Res

Laboratório de Desenvolvimento Galênico (LADEG), Departamento de Fármacos e Medicamentos, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Published: December 2020

AI Article Synopsis

  • Leishmaniasis is caused by Leishmania parasites and affects millions, with current treatments for cutaneous leishmaniasis (CL) having many side effects.
  • The study developed oil-water nanoemulsions (NEs) containing the drug Amphotericin B (AmB) for improved topical treatment of CL, focusing on droplet size, stability, release profile, and anti-leishmanial activity.
  • Results showed that AmB-NEs had a droplet size under 60 nm, excellent stability for a year at refrigeration, controlled drug release, lower skin permeability, and reduced cytotoxicity compared to free AmB, indicating strong potential as a new treatment option for CL.

Article Abstract

Leishmaniasis is a neglected infectious disease caused by protozoan parasites from Leishmania genus species, affecting millions of people, in several countries. The current available treatment for cutaneous leishmaniasis (CL) has presented many side effects. In this way, micro- and nanotechnology are important processes, since they may be useful for release profile modulation of CL drugs improving their bioavailability. Amphotericin B (AmB) is a macrolide antibiotic used as a second-choice treatment. This study aimed the development of oil-water nanoemulsions (NEs) containing AmB for topical administration to treat CL. Furthermore, NEs were characterized by their droplet size, morphology, drug content, stability, in vitro release profile, and ex vivo skin permeation. In vitro anti-leishmanial activity using Leishmania amazonensis promastigotes was also evaluated. NEs containing AmB presented droplet size lower than 60 nm with a polydispersity index lower than 0.5. The best AmB-NEs were submitted to stability tests and these formulations presented excellent results after 365 days under refrigeration, confirming the maintenance of the drug content higher than 95%. AmB-NEs displayed slow and controlled AmB kinetic release and low skin permeation. These formulations presented lower cytotoxicity in comparison with free AmB and higher anti-leishmanial effect against L. amazonensis promastigotes. Therefore, the selected AmB-NE formulations, especially AmB-NE01, presented promising results as novel alternatives for CL treatment. Graphical abstract.

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Source
http://dx.doi.org/10.1007/s13346-020-00821-5DOI Listing

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