首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Development and validation of bioanalytical methods for imidafenacin (KRP-197/ONO-8025) and its metabolites in human urine by using liquid chromatography-tandem mass spectrometry.
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Development and validation of bioanalytical methods for imidafenacin (KRP-197/ONO-8025) and its metabolites in human urine by using liquid chromatography-tandem mass spectrometry.

机译:液相色谱-串联质谱法开发和验证人尿中咪达芬那(KRP-197 / ONO-8025)及其代谢物的生物分析方法。

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New bioanalytical methods have been developed for the determination of imidafenacin (KRP-197/ONO-8025, IM), a novel antimuscarinic drug developed for the treatment of overactive bladder, and its metabolites, M-2, M-3, M-4, M-6 and M-8 (method 1), M-5 and M-9 (method 2) in human urine by using liquid chromatography-tandem mass spectrometry. In each method, the urine sample was extracted by solid-phase extraction, separated on a semi-micro high-performance liquid chromatography column using gradient elution and detected by tandem mass spectrometer with an atmospheric pressure chemical ionization or ionspray interface. Extraction recoveries of IM and metabolites were 81.4% or more. Calibration curves had good linearity in the concentration ranges 0.2-50 ng/mL for IM, M-2, M-3, M-4, M-6 and M-8 (method 1) and 1-250 ng/mL for M-5 and M-9 (method 2), respectively. The accuracy and precision in the intra-day and inter-day reproducibility tests were within +/-17.0 and 16.1% at the lowest concentrations, and within +/-12.8 and 11.1% at higher concentrations, respectively. Using these analytical methods, excretion profiles of IM and its metabolites in human urine were successfully determined after oral administration of IM at the therapeutic dosage of 0.1 mg. Copyright (c) 2007 John Wiley & Sons, Ltd.
机译:已开发出新的生物分析方法来测定咪达芬那胺(KRP-197 / ONO-8025,IM),这是一种用于治疗膀胱过度活动症的新型抗毒蕈碱药物,及其代谢物M-2,M-3,M-4液相色谱-串联质谱法测定人尿中的M,M-6和M-8(方法1),M-5和M-9(方法2)。在每种方法中,尿液样品均通过固相萃取,在半微高效液相色谱柱上使用梯度洗脱进行分离,并通过具有大气压化学电离或离子喷雾界面的串联质谱仪进行检测。 IM和代谢物的提取回收率为81.4%或更高。校正曲线在IM,M-2,M-3,M-4,M-6和M-8(方法1)的浓度范围为0.2-50 ng / mL和M的浓度范围为1-250 ng / mL时具有良好的线性-5和M-9(方法2)。日内和日间重现性测试的准确度和精密度在最低浓度下分别在+/- 17.0和16.1%之内,在最高浓度下分别在+/- 12.8和11.1%之内。使用这些分析方法,以0.1 mg的治疗剂量口服IM后,成功确定了IM及其代谢物在人尿中的排泄曲线。版权所有(c)2007 John Wiley&Sons,Ltd.

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