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Development of a UHPLC-MS/MS method for the quantification of ilaprazole enantiomers in rat plasma and its pharmacokinetic application

机译:大鼠血浆中钛唑对映体定量uHPLC-MS / MS法的研制及其药代动力学应用

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摘要

In Korea and China, ilaprazole is a widely used proton pump inhibitor in the treatment of gastric ulcers. In this study, a specific and sensitive LC-MS/MS method has been developed and validated for the quantification of ilaprazole enantiomers in the rat plasma, using R-lansoprazole as the internal standard. The enantioseparation was achieved on a CHIRALPAK AS-RH column (4.6 mm × 150 mm, i.d. 5 μm), with a mobile phase composed of 10 mM ammonium acetate aqueous solution and acetonitrile (60:40, V/V), at a flow-rate of 0.5 mL/min. The method was validated over the concentration range of 0.5–300 ng/mL for both, R- and S -ilaprazole. The lower limit of quantification was 0.5 ng/mL for both enantiomers. The relative standard deviation (RSD) of intra- and inter-day precision of R-ilaprazole and S-ilaprazole was less than 10.9%, and the relative error accuracy (RE) ranged from −0.5%–2.0%. Finally, the method was successfully evaluated in rats in a stereoselective pharmacokinetic study of the ilaprazole racemate.
机译:在韩国和中国,Ilaprazole是一种广泛使用的质子泵抑制剂,治疗胃溃疡。在该研究中,已经开发了一种特定的和敏感的LC-MS / MS方法并验证了使用R-LansoLazole作为内标在大鼠等离子体中的ilapra唑对映体的定量。在Chiralpak AS-RH柱(4.6mm×150mm,ID5μm)上实现了对映的分子,其流动阶段由10mM乙酸铵水溶液和乙腈(60:40,V / V)组成, - 0.5ml / min。该方法验证在0.5-300ng / ml的浓度范围内,r-和s-lirabrazole。对映体的定量下限为0.5ng / ml。 R-Ilaprazole和S-Ilaprazole的内部和日间精度的相对标准偏差(RSD)小于10.9%,相对误差精度(RE)范围为-0.5%-2.0%。最后,在ILAPRAZOLE外消旋物的立体选择性药代动力学研究中成功评估了该方法。

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