Nanoencapsulação de compostos de rutênio, análise de sua atividade anti - Mycobacterium tuberculosis e biodisponibilidade oral

Detalhes bibliográficos
Ano de defesa: 2015
Autor(a) principal: Freitas, Eduardo Sinesio de [UNESP]
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Estadual Paulista (Unesp)
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://hdl.handle.net/11449/139385
http://www.athena.biblioteca.unesp.br/exlibris/bd/cathedra/31-05-2016/000858669.pdf
Resumo: Tuberculosis (TB) is an infectious airborne disease, curable and mainly affects the lungs. In recent years, the death rate has been decreasing, however, resistant strains and co-infection TB / HIV have hampered the disease control efforts, leading to increased mortality. Another troubling factor is that one third of the world's population is infected with Mycobacterium tuberculosis (MTB) in a state of latency, which serves as a reservoir for active TB. In an effort to remedy this failure, it is increasing the importance of bioinorganic chemistry as an ally in the new anti-TB drug research. The Ruthenium (Ru) is a chemical element that has the capacity to mimic the iron (Fe) in our body, with low toxicity and able to form stable complexes, this element has been studied since the 80's as a possible substitute for platinum (Pt ), the central metal structure of cisplatin used in anticancer treatments. In previous studies involving heteroleptic ruthenium complexes: [Ru(pic)(dppb)(bipy)]PF6 (SCAR1); [Ru(pic)(dppb)(Me-bipy)]PF6 (SCAR2); [Ru(pic)(dppb)(phen)]PF6 (SCAR4); cis-[Ru(pic)(dppe)2]PF6 (SCAR5); cis[RuCl2(dppb)(bipy)] (SCAR6) and [Ru(pic)(dppe)(phen)]PF6 (SCAR7), we observed an excellent anti-TB activity, moderate cell toxicity and lack of oral bioavailability in vivo model of these complexes thus the main objective of this study was to evaluate the toxicity and oral bioavailability of those nano-coated complexes. These nanostructured systems have been developed using different ratios of surfactant (soybean phosphatidylcholine, Emulgin® and sodium oleate), aqueous phase (phosphate buffer pH 7.4) and oil (cholesterol) in order to obtain a system for incorporating the compounds of ruthenium. The system was characterized by analyzes rheology, particle size and zeta potential. The anti-TB activity of the compounds was determined by the microdilution assay with Resazurin (REMA) compared to strains of M. tuberculosis H37Rv and clinical isolates...