Nanostructured Lipid Systems as a Strategy to Improve the in Vitro Cytotoxicity of Ruthenium(II) Compounds

Molecules

Eduardo Sinesio de Freitas³  Patricia Bento da Silva¹  Marlus Chorilli¹  Alzir Azevedo Batista²  Érica de Oliveira Lopes³  Monize Martins da Silva²  Clarice Queico Fujimura Leite³ 

[1] Departamento de Fármacos e Medicamentos, Faculdade de Ciências Farmacêuticas, Universidade Estadual Paulista, Araraquara, São Paulo 14801-902, Brazil;Departamento de Química, Universidade Federal de São Carlos, São Carlos, São Paulo 13565-905, Brazil;Departamento de Ciências Biológicas, Faculdade de Ciências Farmacêuticas, Universidade Estadual Paulista, Araraquara, São Paulo 14801-902, Brazil

关键词: ruthenium complexes;    tuberculosis;    nanostructured lipid systems;   

DOI  :  10.3390/molecules19055999

来源: mdpi

【 摘 要 】

: Tuberculosis is an ancient disease that is still present as a global public health problem. Our group has been investigating new molecules with anti-TB activity. In this context, inorganic chemistry has been a quite promising source of such molecules, with excellent results seen with ruthenium compounds. Nanostructured lipid systems may potentiate the action of drugs by reducing the required dosage and side effects and improving the antimicrobial effects. The aim of this study was to develop a nanostructured lipid system and then characterize and apply these encapsulated compounds (SCARs 1, 2 and 4) with the goal of improving their activity by decreasing the Minimum Inhibitory Concentration (MIC₉₀) and reducing the cytotoxicity (IC₅₀). The nanostructured system was composed of 10% phase oil (cholesterol), 10% surfactant (soy oleate, soy phosphatidylcholine and Eumulgin^®) and 80% aqueous phase (phosphate buffer pH = 7.4). Good activity against Mycobacterium tuberculosis was maintained after the incorporation of the compounds into the nanostructured lipid system, while the cytotoxicity decreased dramatically, in some cases up to 20 times less toxic than the unencapsulated drug.

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.