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采用气相色谱/质谱联用技术测定血浆和尿液中的依那普利及其活性代谢产物依那普利拉。

Determination of enalapril and its active metabolite enalaprilat in plasma and urine by gas chromatography/mass spectrometry.

作者信息

Shioya H, Shimojo M, Kawahara Y

机构信息

Product Development Laboratories, Sankyo Co. Ltd., Tokyo, Japan.

出版信息

Biomed Chromatogr. 1992 Mar-Apr;6(2):59-62. doi: 10.1002/bmc.1130060203.

Abstract

The method for the simultaneous determination of angiotensin-converting enzyme (ACE) inhibitor enalapril and its active metabolite enalaprilat in plasma and urine was developed by gas chromatography/mass spectrometry. Enalapril and enalaprilat in plasma and urine were extracted and cleaned up by using Sep-Pak C18 and silica cartridges. Derivatization was carried out using diazomethane and trifluoroacetic anhydride. Detection by selected ion monitoring was selected to m/z 288 (enalaprilat) and 302 (enalapril). The detection limit of enalapril and enalaprilat was 200 pg/mL in plasma and 2 ng/mL in urine. This method was applied to the pharmacokinetic analysis of enalapril and enalaprilat in body fluids.

摘要

采用气相色谱/质谱法建立了同时测定血浆和尿液中血管紧张素转换酶(ACE)抑制剂依那普利及其活性代谢物依那普利拉的方法。血浆和尿液中的依那普利和依那普利拉用Sep-Pak C18和硅胶柱进行萃取和净化。使用重氮甲烷和三氟乙酸酐进行衍生化反应。通过选择离子监测法进行检测,选择m/z 288(依那普利拉)和302(依那普利)。依那普利和依那普利拉在血浆中的检测限为200 pg/mL,在尿液中的检测限为2 ng/mL。该方法应用于依那普利和依那普利拉在体液中的药代动力学分析。

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