Pharmacokinetic study of AmB-NP-GR: A new granule form with amphotericin B to treat leishmaniasis and fungal infections

Autor(es)

Tadini, Maraine Catarina ; Fernandes, Fernanda Santos ; Ozelin, Saulo Duarte ; Santos de Melo, Matheus Reis ; Mansur, Ana Luiza ; de Toledo, Thais Bueno ; Perez de Albuquerque, Nayara Cristina ; Tavares, Denise Crispim ; Marquele-Oliveira, Franciane ; Moraes de Oliveira, Anderson Rodrigo

• Tipo de documento: Artigo Científico
• Fonte: European Journal of Pharmaceutical Sciences; v. 173, p. 9-pg., 2022-03-28.

Resumo

Amphotericin B (AmB) has been the gold standard to treat systemic fungal infections. The use of AmB is restricted to hospitals because it poses several risks, mainly risks related to its high nephrotoxicity. Given the importance of this drug in medicine, new therapeutics and AmB formulations with nanotechnological improvements are required and could bring many benefits to patients. A new drug formulation with gastro-resistant coated granules has been proposed. The lipid-based system containing AmB was produced and used as raw material in the granulation/coated process. The new developed formulation (AmB-NP-GR) was characterized by optical microscopy, granulometry, and atomic force microscopy (AFM) after disintegration test. AmB-NP-GR showed granular shape, with most granules measured between 250 and 500 mu m (37 +/- 7% w/w). The AFM images indicated that the granule formulation should disintegrate in the intestine, to release the lipid-based carriers, making them available for absorption and allowing them to reach the blood circulation. The developed formulation was administered to rats in a single dose of 4.0 or 8.0 mg kg(-1) and the pharmacokinetics was studied. The samples were analyzed by liquid chromatography coupled to mass spectrometry. Before the pharmacokinetic studies were conducted, the bioanalytical method was validated according to the EMA guideline and all evaluated parameters agreed with this guideline. The pharmacokinetic results showed that C-max was similar for both doses and that t(max) was reached at 4-12 h for dose of 4.0 mg kg(-1) and 4 h for dose of 8.0 mg kg(-1). The half-life related to the dose of 8.0 mg kg(-1) increased significantly compared to the dose of 4.0 mg kg(-1) an increase of more than 3 times). In addition, the mean residence time related to the dose of 8.0 mg kg(-1) was 4 times higher than for the lower dose. The clearance value showed to be higher for the lower dose. Together, these results provide important conclusions for experimental design of other in vivo safety and efficacy studies of AmB-NP-GR. (AU)

• Processo FAPESP: 17/22888-4 - Desenvolvimento e caracterização de medicamento de base nanotecnológica, alvo-dirigido, para tratamento de Leishmaniose
• Beneficiário: Franciane Marquele de Oliveira
• Modalidade de apoio: Auxílio à Pesquisa - Pesquisa Inovativa em Pequenas Empresas - PIPE
• Processo FAPESP: 14/50945-4 - INCT 2014: Instituto Nacional de Tecnologias Alternativas para Detecção, Avaliação Toxicológica e Remoção de Micropoluentes e Radioativos
• Beneficiário: Maria Valnice Boldrin
• Modalidade de apoio: Auxílio à Pesquisa - Temático
• Processo FAPESP: 18/07534-4 - Desenvolvimento de métodos cromatográficos/eletroforéticos para posterior aplicação em estudos in vitro de inibição enzimática e predição de interações medicamentosas de praguicidas quirais - Fase 2
• Beneficiário: Anderson Rodrigo Moraes de Oliveira
• Modalidade de apoio: Auxílio à Pesquisa - Regular