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首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Determination of Ramipril and its Active Metabolite Ramiprilat from Plasma by Liquid Chromatography-Mass Spectrometry for Bioequivalence Studies
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Determination of Ramipril and its Active Metabolite Ramiprilat from Plasma by Liquid Chromatography-Mass Spectrometry for Bioequivalence Studies

机译:液相色谱-质谱法测定血浆中雷米普利及其活性代谢物雷米普利拉特的生物等效性

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摘要

Ramipril and ramiprilat were isolated by solid phase extraction using PROSPEKT-2,which is an online solid phase extractor.This method is suitable for bioequivalence studies following single dose in healthy volunteers.This assay achieved higher sensitivity and better specificity for the analysis of ramipril and ramiprilat in human plasma.The limit of quantitation of 0.25 ng/mL for ramipril and ramiprilat was thus attainable by high performance liquid chromatography mass spectrometry (HPLC-MS/MS).The internal standard proved to be a good internal standard for this assay.No significant interference caused by endogenous compounds was observed.This simple and rapid assay can be successfully used in pharmacokinetic studies of ramipril and ramiprilat.
机译:雷米普利和雷米普利拉是通过在线固相萃取器PROSPEKT-2固相萃取分离的,此方法适用于健康志愿者单剂量后的生物等效性研究,该测定方法对雷米普利和雷米普利的分析具有更高的灵敏度和更好的特异性。高效液相色谱质谱法(HPLC-MS / MS)可确定雷米普利和雷米普利拉的定量限为0.25 ng / mL,内标被证明是该测定的良好内标。没有观察到内源性化合物引起的显着干扰。这种简单,快速的测定方法可成功用于雷米普利和雷米普利拉的药代动力学研究。

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