Shioya H, Shimojo M, Kawahara Y
Product Development Laboratories, Sankyo Co. Ltd., Tokyo, Japan.
Biomed Chromatogr. 1992 Mar-Apr;6(2):59-62. doi: 10.1002/bmc.1130060203.
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.
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。