Liposomal amphotericin b for treatment of leishmaniasis: from the identification of critical physicochemical attributes to the design of effective topical and oral formulations

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Tipo

Artigo de periódico

Título alternativo

Primeiro orientador

Membros da banca

Resumo

The liposomal amphotericin B (AmB) formulation, AmBisome®, still represents the best therapeutic option for cutaneous and visceral leishmaniasis. However, its clinical efficacy depends on the patient’s immunological status, the clinical manifestation and the endemic region. Moreover, the need for parenteral administration, its side effects and high cost significantly limit its use in developing countries. This review reports the progress achieved thus far toward the understanding of the mechanism responsible for the reduced toxicity of liposomal AmB formulations and the factors that influence their efficacy against leishmaniasis. It also presents the recent advances in the development of more effective liposomal AmB formulations, including topical and oral liposome formulations. The critical role of the AmB aggregation state and release rate in the reduction of drug toxicity and in the drug efficacy by non-invasive routes is emphasized. This paper is expected to guide future research and development of innovative liposomal formulations of AmB.

Abstract

Assunto

Lipossomos, Anfotericina B, Anfotericina B, Leishmaniose, Vias de administração de medicamentos

Palavras-chave

liposomes, Amphotericin B, Leishmaniasis, Oral route, PEGylation, Topical route

Citação

Curso

Endereço externo

https://www.mdpi.com/1999-4923/15/1/99

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