Dickinson Laura, Robinson Lesley, Tjia John, Khoo Saye, Back David
Department of Pharmacology, University of Liverpool, Pharmacology Research Laboratories, Block H, First Floor, 70 Pembroke Place, Liverpool L69 3GF, UK.
J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Dec 27;829(1-2):82-90. doi: 10.1016/j.jchromb.2005.09.032. Epub 2005 Oct 13.
We report a precise and accurate method for simultaneous quantification of protease inhibitors (PIs) amprenavir, atazanavir, indinavir, lopinavir, nelfinavir, ritonavir and saquinavir in plasma. An internal standard was added to samples prior to protein precipitation with acetonitrile followed by addition of ammonium formate buffer. Analysis was by HPLC-MS/MS. Calibration curves were validated over concentration ranges encompassing both subtherapeutic and potentially 'toxic' drug concentrations. Inter- and intra-assay variation were below 11% and PI recovery was above 87%. The bioanalytical method described is successfully applied to measure PI concentrations obtained from clinical pharmacokinetic studies and routine therapeutic drug monitoring (TDM).
我们报告了一种精确且准确的方法,用于同时定量测定血浆中的蛋白酶抑制剂(PI)安普那韦、阿扎那韦、茚地那韦、洛匹那韦、奈非那韦、利托那韦和沙奎那韦。在使用乙腈进行蛋白沉淀之前,向样品中加入内标,随后加入甲酸铵缓冲液。通过高效液相色谱-串联质谱法(HPLC-MS/MS)进行分析。校准曲线在涵盖亚治疗浓度和潜在“毒性”药物浓度的浓度范围内得到验证。批间和批内变异低于11%,PI回收率高于87%。所描述的生物分析方法已成功应用于测量临床药代动力学研究和常规治疗药物监测(TDM)中获得的PI浓度。