首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of imigliptin and its three metabolites in human plasma and urine by liquid chromatography coupled to tandem mass spectrometry
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Simultaneous determination of imigliptin and its three metabolites in human plasma and urine by liquid chromatography coupled to tandem mass spectrometry

机译:液相色谱-串联质谱法同时测定人血浆和尿液中伊格列汀及其三种代谢物

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摘要

A specific and sensitive method was firstly developed using high performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS) to simultaneously quantify imigliptin (KBP-3853) and its three metabolites (KBP-3926, KBP-3902, KBP-5493) in human plasma and urine. Solid-phase extraction (SPE) and direct dilution were used to extract imigliptin and its three metabolites from plasma and urine, respectively. The extracts were injected onto a SymmetryShield RP8 column with a gradient elution of acetonitrile and water containing 5 mM ammonium acetate (pH 7). Ionization of KBP-3853, KBP-3926, KBP-3902, KBP-5493, and XZP-3244 (internal standard, IS) was performed using an electrospray ionization (ESI) source in positive mode and detection was carried out with multiple reaction monitoring (MRM) mode. The lower limits of quantitation (LLOQ) of KBP-3853/KBP-3926/KBP-3902/KBP-5493 in human plasma and urine were 0.500/0.500/0.500/0.500ng/mL and 20.0/20.0/10.0/10.0 ng/mL, respectively. Inter- and intra-batch precision of imigliptin and its three metabolites were less than 15% and the accuracy was within 85-115% for both plasma and urine. The extraction recoveries of all analytes at three concentration levels were consistent. The specificity, matrix effect, linearity and stabilities under various conditions were validated for imigliptin and its three metabolites in human plasma and urine. In conclusion, the validation results showed that this method was robust, specific, and sensitive and it can successfully fulfill the requirement of clinical pharmacokinetic study of imigliptin hydrochloride in Chinese healthy subjects. (C) 2015 Elsevier B.V. All rights reserved.
机译:首先使用高效液相色谱和串联质谱(HPLC-MS / MS)来开发一种特异性灵敏的方法,以同时定量伊格列汀(KBP-3853)及其三种代谢物(KBP-3926,KBP-3902,KBP-5493 )在人体血浆和尿液中。固相萃取(SPE)和直接稀释分别用于从血浆和尿液中提取伊格列汀及其三种代谢物。将萃取液注射到SymmetryShield RP8色谱柱上,用乙腈和含有5 mM乙酸铵(pH 7)的水进行梯度洗脱。使用电喷雾电离(ESI)源以正模式对KBP-3853,KBP-3926,KBP-3902,KBP-5493和XZP-3244(内标IS)进行电离,并通过多反应监测进行检测(MRM)模式。人血浆和尿液中KBP-3853 / KBP-3926 / KBP-3902 / KBP-5493的定量下限(LLOQ)为0.500 / 0.500 / 0.500 / 0.500ng / mL和20.0 / 20.0 / 10.0 / 10.0 ng / mL mL,分别。伊格列汀及其三种代谢物的批间和批内精度均低于15%,血浆和尿液的精度均在85-115%之内。在三个浓度水平下所有分析物的提取回收率是一致的。验证了伊格列汀及其在人体血浆和尿液中的三种代谢产物在各种条件下的特异性,基质效应,线性和稳定性。综上所述,验证结果表明该方法可靠,特异,灵敏,可以成功地满足中国健康受试者对盐酸伊格列汀的临床药代动力学研究的要求。 (C)2015 Elsevier B.V.保留所有权利。

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