CiPharma-Programa de Pós-graduação em Ciências Farmacêuticas, Escola de Farmácia, Universidade Federal de Ouro Preto, Rua Costa Sena, 171-Centro, Ouro Preto 35400-000, Minas Gerais, MG, Brazil.
J Pharm Biomed Anal. 2011 Aug 25;56(1):70-7. doi: 10.1016/j.jpba.2011.04.016. Epub 2011 Apr 22.
Analytical and bioanalytical methods of high-performance liquid chromatography with fluorescence detection (HPLC-FLD) were developed and validated for the determination of chloroaluminum phthalocyanine in different formulations of polymeric nanocapsules, plasma and livers of mice. Plasma and homogenized liver samples were extracted with ethyl acetate, and zinc phthalocyanine was used as internal standard. The results indicated that the methods were linear and selective for all matrices studied. Analysis of accuracy and precision showed adequate values, with variations lower than 10% in biological samples and lower than 2% in analytical samples. The recoveries were as high as 96% and 99% in the plasma and livers, respectively. The quantification limit of the analytical method was 1.12 ng/ml, and the limits of quantification of the bioanalytical method were 15 ng/ml and 75 ng/g for plasma and liver samples, respectively. The bioanalytical method developed was sensitive in the ranges of 15-100 ng/ml in plasma and 75-500 ng/g in liver samples and was applied to studies of biodistribution and pharmacokinetics of AlClPc.
建立并验证了高效液相色谱-荧光检测法(HPLC-FLD)分析和生物分析方法,用于测定不同聚合物纳米胶囊配方、小鼠血浆和肝脏中氯代铝酞菁的含量。采用乙酸乙酯提取血浆和匀浆肝样品,以锌酞菁作为内标。结果表明,该方法对所有研究基质均具有线性和选择性。分析准确度和精密度的结果表明,生物样品的变异低于 10%,分析样品的变异低于 2%。血浆和肝脏中的回收率分别高达 96%和 99%。分析方法的定量限为 1.12ng/ml,生物分析方法的定量限分别为血浆和肝脏样品的 15ng/ml 和 75ng/g。所建立的生物分析方法在血浆中 15-100ng/ml 范围内和肝脏中 75-500ng/g 范围内具有较高的灵敏度,并应用于 AlClPc 的生物分布和药代动力学研究。