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A new nanoemulsion formulation improves antileishmanial activity and reduces toxicity of amphotericin B.
Santos, Délia Chaves Moreira Dos; de Souza, Marselle Leite Silvério; Teixeira, Eliane Morais; Alves, Líndicy Leidicy; Vilela, José Mário Carneiro; Andrade, Margareth; Carvalho, Maria das Graças; Fernandes, Ana Paula; Ferreira, Lucas Antônio Miranda; Aguiar, Marta Marques Gontijo.
Afiliação
  • Santos DCMD; a Department of Pharmaceutics, Faculty of Pharmacy , Federal University of Minas Gerais (UFMG) , Belo Horizonte , Minas Gerais , Brazil.
  • de Souza MLS; a Department of Pharmaceutics, Faculty of Pharmacy , Federal University of Minas Gerais (UFMG) , Belo Horizonte , Minas Gerais , Brazil.
  • Teixeira EM; b Laboratory of Clinical Research , Instituto René Rachou, Fundação Oswaldo Cruz-Fiocruz , Belo Horizonte , Minas Gerais , Brazil.
  • Alves LL; b Laboratory of Clinical Research , Instituto René Rachou, Fundação Oswaldo Cruz-Fiocruz , Belo Horizonte , Minas Gerais , Brazil.
  • Vilela JMC; c Centro de Inovação e Tecnologia Senai Fiemg - Campus CETEC , Belo Horizonte , Minas Gerais , Brazil.
  • Andrade M; c Centro de Inovação e Tecnologia Senai Fiemg - Campus CETEC , Belo Horizonte , Minas Gerais , Brazil.
  • Carvalho MDG; d Department of Clinical and Toxicological Analysis , Faculty of Pharmacy, Federal University of Minas Gerais (UFMG) , Belo Horizonte , Minas Gerais , Brazil.
  • Fernandes AP; d Department of Clinical and Toxicological Analysis , Faculty of Pharmacy, Federal University of Minas Gerais (UFMG) , Belo Horizonte , Minas Gerais , Brazil.
  • Ferreira LAM; a Department of Pharmaceutics, Faculty of Pharmacy , Federal University of Minas Gerais (UFMG) , Belo Horizonte , Minas Gerais , Brazil.
  • Aguiar MMG; a Department of Pharmaceutics, Faculty of Pharmacy , Federal University of Minas Gerais (UFMG) , Belo Horizonte , Minas Gerais , Brazil.
J Drug Target ; 26(4): 357-364, 2018 04.
Article em En | MEDLINE | ID: mdl-29041824
This work aimed to optimise a new nanoemulsion (NE) formulation loaded with Amphotericin B (AmB) and to evaluate its in vivo antileishmanial activity and in vitro haemolytic toxicity. The influence of gradual increases in pressure, using a high-pressure homogeniser, was evaluated. The NE was characterised for droplet size, polydispersity index, zeta potential and encapsulation efficiency (EE). For antileishmanial activity studies, AmB-NE was administered intravenously in mice infected by Leishmania infantum chagasi, which causes Visceral Leishmaniasis (VL). When the NE was submitted to gradual increases in pressure, the PI values and droplet size decreased. The droplet size (∼145 nm) was lower than that obtained in previous studies. The zeta potential was negative and the EE was almost 100%. The haemolytic toxicity, evaluated on human red blood cells, for AmB-loaded NE was lower than that observed for the conventional AmB (C-AmB). C-AmB at 2 mg/kg was very toxic. In contrast, administration of the AmB-loaded NE, at same dose, did not result in any sign of acute toxicity, promoting a significant reduction in parasite burden as compared to the C-AmB. These findings suggest that this new AmB-loaded NE constitutes an attractive alternative for the treatment of VL due to improved efficacy and lower toxicity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anfotericina B / Nanopartículas / Leishmaniose Visceral / Antiprotozoários Limite: Animals / Female / Humans Idioma: En Revista: J Drug Target Assunto da revista: FARMACOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anfotericina B / Nanopartículas / Leishmaniose Visceral / Antiprotozoários Limite: Animals / Female / Humans Idioma: En Revista: J Drug Target Assunto da revista: FARMACOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido