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

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          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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          Author and article information

          Journal
          Drug Deliv Transl Res
          Drug delivery and translational research
          Springer Science and Business Media LLC
          2190-3948
          2190-393X
          December 2020
          : 10
          : 6
          Affiliations
          [1 ] Laboratório de Desenvolvimento Galênico (LADEG), Departamento de Fármacos e Medicamentos, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil. anapaulasmatos@gmail.com.
          [2 ] Laboratório de Farmacotécnica Experimental, Instituto de Tecnologia em Fármacos - Farmanguinhos, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brazil. anapaulasmatos@gmail.com.
          [3 ] Laboratório Multidisciplinar de Ciências Farmacêuticas, Departamento de Fármacos e Medicamentos, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil. anapaulasmatos@gmail.com.
          [4 ] Laboratório de Desenvolvimento Galênico (LADEG), Departamento de Fármacos e Medicamentos, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
          [5 ] Laboratório de Farmacotécnica Experimental, Instituto de Tecnologia em Fármacos - Farmanguinhos, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brazil.
          [6 ] Laboratório Multidisciplinar de Ciências Farmacêuticas, Departamento de Fármacos e Medicamentos, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
          [7 ] BIOINOVAR - Laboratório de Biotecnologia, Unidade de Biocatálise, Bioprodutos e Bioenergia, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
          [8 ] Comissão Brasileira de Energia Nuclear, Instituto de Engenharia Nuclear, Rio de Janeiro, RJ, Brazil.
          Article
          10.1007/s13346-020-00821-5
          10.1007/s13346-020-00821-5
          32676952
          0c7a1b37-156e-40c4-af45-7b570e33bcbf
          History

          Nanoemulsions,Amphotericin B,Cutaneous leishmaniasis,Ex vivo skin permeation study,In vitro assessments,In vitro release study

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