Proust V, Toth K, Hulin A, Taburet A M, Gimenez F, Singlas E
Hôpital Necker Enfants Malades, Service Pharmacie, Paris, France.
J Chromatogr B Biomed Sci Appl. 2000 Jun 9;742(2):453-8. doi: 10.1016/s0378-4347(00)00208-5.
This article describes a method for the simultaneous determination of four licensed HIV protease inhibitors (amprenavir, nelfinavir, saquinavir and ritonavir) and two novel non-nucleoside reverse transcriptase inhibitors (efavirenz and delavirdine) in human plasma in a single run. Plasma samples (500 microl) were treated by liquid-liquid extraction with methyl tert.-butyl ether. The compounds were separated by reversed-phase liquid chromatography on a C(18) column with spectrophotometric detection at 260 nm. The method is linear over the specific ranges investigated, accurate (inaccuracy <11.7%) and showed intra-day and inter-day precision within the ranges of 0.9-7.0 and 1.9-8.8%, respectively. The six compounds were stable in plasma after 6 months of storage at -20 degrees C and after five freeze-thaw cycles.
本文介绍了一种可在一次分析中同时测定人血浆中四种已获许可的HIV蛋白酶抑制剂(安普那韦、奈非那韦、沙奎那韦和利托那韦)以及两种新型非核苷类逆转录酶抑制剂(依非韦伦和地拉韦啶)的方法。血浆样本(500微升)用甲基叔丁基醚进行液液萃取处理。这些化合物在C(18)柱上通过反相液相色谱法分离,并在260纳米处进行分光光度检测。该方法在所研究的特定范围内呈线性,准确(误差<11.7%),日内和日间精密度分别在0.9 - 7.0%和1.9 - 8.8%范围内。这六种化合物在-20℃储存6个月以及经过五次冻融循环后在血浆中仍保持稳定。