Hirabayashi Yoshihiro, Tsuchiya Kiyoto, Kimura Satoshi, Oka Shinichi
AIDS Clinical Center, International Medical Center of Japan, 1-21-1 Toyama, Shinjuku-ku, Tokyo 162-8655, Japan.
Biomed Chromatogr. 2006 Jan;20(1):28-36. doi: 10.1002/bmc.521.
We report the development of a simple, economical and reliable chromatographic method for the simultaneous determination of six HIV protease inhibitors (PIs; amprenavir, indinavir, lopinavir, nelfinavir, ritonavir and saquinavir), the active metabolite of nelfinavir (M8) and the non-nucleoside reverse transcriptase inhibitor (NNRTI; efavirenz) in human plasma. After extraction from plasma with an ethyl acetate-acetonitrile mixture, the analytes were separated on a phenyl column with a gradient of acetonitrile and phosphate solutions, and detected at three ultraviolet wavelengths. Calibration curves were linear over the range 0.025-15 microg/mL for saquinavir and 0.05-15 microg/mL for the other analytes. The accuracies ranged from -6.9% to +7.6%, and the intra-assay and inter-assay precisions were <9.2 and <11.8%, respectively. Our method, covering most of the PIs and NNRTIs currently used, facilitates ready therapeutic drug monitoring in hospital laboratories.
我们报告了一种简单、经济且可靠的色谱方法的开发,该方法用于同时测定人血浆中的六种HIV蛋白酶抑制剂(PIs;安普那韦、茚地那韦、洛匹那韦、奈非那韦、利托那韦和沙奎那韦)、奈非那韦的活性代谢物(M8)以及非核苷类逆转录酶抑制剂(NNRTI;依非韦伦)。用乙酸乙酯 - 乙腈混合物从血浆中萃取后,分析物在苯基柱上用乙腈和磷酸盐溶液梯度分离,并在三个紫外波长下进行检测。沙奎那韦的校准曲线在0.025 - 15μg/mL范围内呈线性,其他分析物在0.05 - 15μg/mL范围内呈线性。准确度范围为 - 6.9%至 + 7.6%,批内精密度和批间精密度分别<9.2%和<11.8%。我们的方法涵盖了目前使用的大多数PIs和NNRTIs,便于医院实验室进行常规治疗药物监测。