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首页> 外文期刊>Chromatographia >Simultaneous determination of six HIV protease inhibitors, one metabolite, and two non-nucleoside reverse transcriptase inhibitors in human plasma by isocratic reversed-phase liquid chromatography after solid-phase extraction
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Simultaneous determination of six HIV protease inhibitors, one metabolite, and two non-nucleoside reverse transcriptase inhibitors in human plasma by isocratic reversed-phase liquid chromatography after solid-phase extraction

机译:固相萃取后通过等度反相液相色谱法同时测定人血浆中的6种HIV蛋白酶抑制剂,1种代谢物和2种非核苷类逆转录酶抑制剂

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A selective and sensitive high-performance liquid chromatographic (HPLC) method has been developed and validated for the determination of six human immunodeficiency virus (HIV)-protease inhibitors (amprenavir, indinavir, lopinavir, nelfinavir, ritonavir, and saquinavir) and two non-nucleoside reverse transcriptase inhibitors (efavirenz and nevirapine) in a single run. This involve a simple liquid-solid extraction on OASIS((R)) HLB column in the presence of an internal standard (prazepam). Separation is achieved on a Xterra((R)), C-18 (150 x 3.9 mm I. D.) column with a mobile phase consisting of acetonitrile and 3-(cyclohexylamino)-1-propane-sulfonic acid (CAPS) buffer pH 10.5, (37 : 63, v/v) delivered isocratically. A sequential ultraviolet detection (5 minutes sequence set at 320 nm for nevirapine acquisition and 55 minutes at 210 nm for other durgs and internal standard) is performed. The method is linear over the specific ranges investigated. Precision and accuracy at four concentrations are respectively less than 13.6% and 9.1% for intraday assays and less than 4.2% and 5.9% for interday assays. This method is suitable for therapeutic drug monitoring purpose and routinely used in our laboratory. [References: 34]
机译:已开发出一种选择性灵敏的高效液相色谱(HPLC)方法,并已用于确定六种人类免疫缺陷病毒(HIV)蛋白酶抑制剂(amprenavir,indinavir,lopinavir,nelfinavir,ritonavir和saquinavir)和两种非一次即可检测到核苷类逆转录酶抑制剂(依非韦伦和奈韦拉平)。这涉及在存在内标物(吡西am)的情况下在OASIS HLB柱上的简单液-固萃取。在Xterra(R)C-18(150 x 3.9 mm内径)色谱柱上进行分离,色谱柱的流动相为乙腈和3-(环己基氨基)-1-丙烷-磺酸(CAPS)缓冲液pH 10.5, (37:63,v / v)等度地投放。进行了连续的紫外线检测(对于奈韦拉平采集,将5分钟的序列设置为320 nm,对于其他标记和内标,将其设置为210 nm的55分钟)。该方法在研究的特定范围内是线性的。对于日间测定,四种浓度下的精密度和准确度分别小于13.6%和9.1%,对于日间测定,分别小于4.2%和5.9%。此方法适用于治疗药物监测目的,通常在我们的实验室中使用。 [参考:34]

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