Masuda Yuichi, Kanayama Norihiro, Manita Shigeru, Ohmori Satoshi, Ooie Tsuyoshi
Research Center, Kyorin Pharmaceutical Co. Ltd, 1848, Nogi, Nogi-machi, Shimotsuga-gun, Tochigi 329-0114, Japan.
Biomed Chromatogr. 2007 Sep;21(9):940-8. doi: 10.1002/bmc.837.
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.
已开发出新型生物分析方法,用于测定咪达那新(KRP - 197/ONO - 8025,IM)及其代谢物M - 2、M - 3、M - 4、M - 6和M - 8(方法1)、M - 5和M - 9(方法2),咪达那新是一种开发用于治疗膀胱过度活动症的新型抗毒蕈碱药物,该方法采用液相色谱 - 串联质谱法检测人尿液中的上述物质。在每种方法中,尿液样本通过固相萃取进行提取,在半微高效液相色谱柱上使用梯度洗脱进行分离,并通过带有大气压化学电离或离子喷雾接口的串联质谱仪进行检测。IM及其代谢物的提取回收率均在81.4%以上。校准曲线在浓度范围分别为0.2 - 50 ng/mL(针对IM、M - 2、M - 3、M - 4、M - 6和M - 8,方法1)和1 - 250 ng/mL(针对M - 5和M - 9,方法2)时具有良好的线性。日内和日间重现性测试中,最低浓度时的准确度和精密度分别在±17.0%和16.1%以内,较高浓度时分别在±12.8%和11.1%以内。使用这些分析方法,成功测定了在以0.1 mg治疗剂量口服IM后,其在人尿液中的排泄情况。