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一种用于定量检测感染人类免疫缺陷病毒(HIV)患者血浆中奈韦拉平、茚地那韦、阿扎那韦、安普那韦、沙奎那韦、利托那韦、洛匹那韦、依非韦伦、替拉那韦、达芦那韦和马拉维罗的液相色谱 - 串联质谱分析法。

A liquid chromatography-tandem mass spectrometry assay for quantification of nevirapine, indinavir, atazanavir, amprenavir, saquinavir, ritonavir, lopinavir, efavirenz, tipranavir, darunavir and maraviroc in the plasma of patients infected with HIV.

作者信息

Martin J, Deslandes G, Dailly E, Renaud C, Reliquet V, Raffi F, Jolliet P

机构信息

Clinical Pharmacology Department, CHU de Nantes, Nantes, France.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Oct 1;877(27):3072-82. doi: 10.1016/j.jchromb.2009.07.031. Epub 2009 Aug 3.

Abstract

A liquid chromatography-tandem mass spectrometry assay for simultaneous determination of the plasma concentration of 11 antiretroviral agents (nevirapine, indinavir, atazanavir, amprenavir, saquinavir, ritonavir, lopinavir, efavirenz, tipranavir, darunavir and maraviroc) has been developed. Sample pre-treatment is limited to protein precipitation with a mixture of methanol and zinc sulfate. After centrifugation the supernatant is injected in the chromatographic system, which consists of on-line solid phase extraction followed by separation on a phenyl-hexyl column. This method, with its simple sample preparation provides sensitive, accurate and precise quantification of the plasma concentration of antiretroviral drugs and can be used for therapeutic drug monitoring in patients infected with HIV.

摘要

已开发出一种液相色谱 - 串联质谱分析法,用于同时测定11种抗逆转录病毒药物(奈韦拉平、茚地那韦、阿扎那韦、安普那韦、沙奎那韦、利托那韦、洛匹那韦、依非韦伦、替拉那韦、达芦那韦和马拉维罗)的血浆浓度。样品预处理仅限于用甲醇和硫酸锌的混合物进行蛋白沉淀。离心后,将上清液注入色谱系统,该系统由在线固相萃取和苯基己基柱分离组成。该方法样品制备简单,能灵敏、准确且精确地定量抗逆转录病毒药物的血浆浓度,可用于HIV感染患者的治疗药物监测。

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