Escola de Farmácia, Universidade Federal de Ouro Preto, Ouro Preto-MG, Brazil.
Eur J Pharm Biopharm. 2011 Aug;78(3):377-84. doi: 10.1016/j.ejpb.2011.03.003. Epub 2011 Mar 17.
Benznidazole (BNZ) is traditionally used to treat Chagas disease. Despite its common use, BNZ has a poor water solubility and a variable bioavailability. The purpose of this study was to prepare BNZ microcrystals by solvent change precipitation and to study the effects of BNZ micronisation on therapeutic efficiency using a murine model of Chagas disease. The solvent change precipitation procedure was optimised in order to obtain stable and homogeneous particles with a small particle size, high yield and fast dissolution rate. The thermal and crystallographic analysis showed no polymorphic change in the microcrystals, and microscopy confirmed a significant reduction in particle size. A marked improvement in the drug dissolution rate was observed for micronised BNZ particles and BNZ tablets in comparison with untreated BNZ and commercial Rochagan. In vivo studies showed a significant increase in the therapeutic efficacy of the BNZ microparticles, corroborating the dissolution results.
苯硝唑(BNZ)传统上用于治疗恰加斯病。尽管其应用广泛,但 BNZ 的水溶性差,生物利用度不稳定。本研究旨在通过溶剂改变沉淀法制备 BNZ 微晶体,并通过恰加斯病的小鼠模型研究 BNZ 微米化对治疗效果的影响。为了获得具有小粒径、高收率和快速溶解速率的稳定且均匀的颗粒,对溶剂改变沉淀程序进行了优化。热分析和结晶分析显示微晶体没有多晶型变化,显微镜观察证实粒径明显减小。与未处理的 BNZ 和商业 Rochagan 相比,微米化 BNZ 颗粒和 BNZ 片剂的药物溶解速率有明显提高。体内研究表明 BNZ 微粒子的治疗效果有显著提高,这与溶解结果相符。