首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Development and validation of a liquid chromatographic-tandem mass spectrometric method for the multiplexed quantification of etravirine, maraviroc, raltegravir, and rilpivirine in human plasma and tissue
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Development and validation of a liquid chromatographic-tandem mass spectrometric method for the multiplexed quantification of etravirine, maraviroc, raltegravir, and rilpivirine in human plasma and tissue

机译:液相色谱-串联质谱法在人血浆和组织中依曲韦林,马拉维罗克,拉格列韦和利比韦林的多重定量分析方法的开发和验证

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摘要

Background: Analytical methodologies for antiretroviral (ARV) quantification are important in determining both systemic and localized drug concentrations. The CCR5-antagonist maraviroc (MVC), the non-nucleoside reverse transcriptase inhibitors (NNRTIs) etravirine (ETV) and rilpivirine (RPV), as well as the integrase strand transfer inhibitor (INSTI) raltegravir (RAL), have all been evaluated using both oral and non-oral dosing regimens, demonstrating a need for dynamic and sensitive bioanalytical tools for drug quantification in plasma and tissue.
机译:背景:抗逆转录病毒(ARV)定量分析方法对于确定全身和局部药物浓度均很重要。 CCR5拮抗剂maraviroc(MVC),非核苷逆转录酶抑制剂(NNRTIs)依曲韦林(ETV)和rilpivirine(RPV)以及整合酶链转移抑制剂(INSTI)raltegravir(RAL)均经过评估无论是口服还是非口服给药方案,都表明需要动态和灵敏的生物分析工具来定量血浆和组织中的药物。

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