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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of the antiretroviral agents: amprenavir, lopinavir, ritonavir, saquinavir and efavirenz in human peripheral blood mononuclear cells by high-performance liquid chromatography-mass spectrometry
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Simultaneous determination of the antiretroviral agents: amprenavir, lopinavir, ritonavir, saquinavir and efavirenz in human peripheral blood mononuclear cells by high-performance liquid chromatography-mass spectrometry

机译:高效液相色谱-质谱法同时测定人外周血单个核细胞中的抗逆转录病毒药物:氨普那韦,洛匹那韦,利托那韦,沙奎那韦和依非韦伦

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A selective and accurate assay for the simultaneous quantitation of four protease inhibitors (PIs) (amprenavir (APV), lopinavir (LPV), ritonavir (RTV) and saquinavir (SQV)) and a non-nucleoside reverse transcriptase inhibitor (NNRTI) (efavirenz, EFV) in human peripheral blood mononuclear cells using high-performance liquid chromatography-mass chromatography (LC/MS) has been developed and validated. After liquid-liquid extraction, the antiretroviral agents were separated within 15 min. The calibration curves of each drug showed a good linearity in a range of concentration between 2 and 200 ng/3 x 10(6) cells for amprenavir, lopinavir, efavirenz, 1.60 and 128 ng/3 x 10(6) cells for ritonavir and saquinavir. Mean intra- and inter-assay coefficients of variation over the ranges of the standard curves were less than 15% and mean extraction recoveries ranged 88.7-112.1%. The limits of quantification were 2ng/3 x 10(6) cells for amprenavir, lopinavir, efavirenz, 1 ng/3 x 10(6) cells for ritonavir and 1.6 ng/3 x 10(6) cells for saquinavir. This novel LC/MS assay, which provides an excellent method for simultaneous intra-cellular determination of amprenavir, lopinavir, ritonavir, saquinavir and efavirenz in human peripheral blood monormclear cells, could be successfully applied for therapeutic drug monitoring and pharmacokinetic studies. (C) 2004 Elsevier B.V. All rights reserved.
机译:同时定量四种蛋白酶抑制剂(PIs)(amprenavir(APV),lopinavir(LPV),ritonavir(RTV)和saquinavir(SQV))和非核苷逆转录酶抑制剂(NNRTI)的选择性准确测定法(efavirenz已经开发并验证了使用高效液相色谱-质谱(LC / MS)在人外周血单核细胞中提取的EFV)。液液萃取后,抗逆转录病毒药物在15分钟内分离。每种药物的校准曲线在2到200 ng / 3 x 10(6)细胞的浓度范围内,对于安普那韦,洛匹那韦,依非韦伦,1.60和128 ng / 3 x 10(6)细胞,对于利托那韦和苯丙酸沙奎那韦。在标准曲线范围内,平均批内和批内变异系数小于15%,平均提取回收率在88.7-112.1%之间。定量限为氨普那韦,洛匹那韦,依非韦伦2ng / 3 x 10(6)细胞,利托那韦1 ng / 3 x 10(6)细胞和沙奎那韦1.6 ng / 3 x 10(6)细胞。这种新颖的LC / MS分析方法为同时检测人外周血单个核细胞中的氨普那韦,洛匹那韦,利托那韦,沙奎那韦和依非韦伦提供了极好的方法,可以成功地用于治疗药物监测和药代动力学研究。 (C)2004 Elsevier B.V.保留所有权利。

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