Sato Yu, Kondo Hiroki, Sato Yuji, Abe Ai, Kikuchi Masafumi, Sato Toshihiro, Kumondai Masaki, Yoshikawa Kohei, Hayakawa Yoshihiro, Maekawa Masamitsu, Mano Nariyasu
Department of Pharmaceutical Sciences, Tohoku University Hospital, 1-1 Seiryo-machi, Aoba-ku, Sendai 980-8574, Japan.
Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan.
Pharmaceutics. 2024 Aug 28;16(9):1138. doi: 10.3390/pharmaceutics16091138.
Therapeutic drug monitoring (TDM) is a personalized treatment approach that involves optimizing drug dosages based on patient-specific factors, such as drug plasma concentrations, therapeutic efficacy, or adverse reactions. The plasma concentration of drugs is determined using liquid chromatography/tandem mass spectrometry (LC-MS/MS) or various immunoassays. Compared with immunoassays, LC-MS/MS requires more pretreatment time as the number of samples increases. Recently, fully automated pretreatment LC-MS/MS systems have been developed to automatically perform whole-sample pretreatment for LC-MS/MS analysis. In this study, we developed a method for simultaneous concentration determination of five analytes (clozapine, mycophenolic acid, sunitinib, -desethylsunitinib, and voriconazole) using LC-MS/MS for clinical TDM using a fully automated LC-MS/MS pretreatment system. In the developed method, the intra- and inter-assay relative error (RE) values ranged between -14.8% and 11.3%; the intra- and inter-assay coefficient of variation (CV) values were <8.8% and <10.5%, respectively. The analytes showed good stability, with RE values ranging between -13.6% and 10.9% and CV values <8.9%. Furthermore, the plasma concentrations in clinical samples using this method and the conventional manual pretreatment method showed similar results. Therefore, the method developed in this study could be considered a useful pretreatment method for routine TDM in patients.
治疗药物监测(TDM)是一种个性化治疗方法,涉及根据患者特定因素(如药物血浆浓度、治疗效果或不良反应)优化药物剂量。药物的血浆浓度通过液相色谱/串联质谱法(LC-MS/MS)或各种免疫测定法来确定。与免疫测定法相比,随着样品数量的增加,LC-MS/MS需要更多的预处理时间。最近,已经开发出全自动预处理LC-MS/MS系统,以自动对LC-MS/MS分析进行全样品预处理。在本研究中,我们开发了一种使用LC-MS/MS和全自动LC-MS/MS预处理系统同时测定五种分析物(氯氮平、霉酚酸、舒尼替尼、去乙基舒尼替尼和伏立康唑)浓度的方法,用于临床TDM。在开发的方法中,批内和批间相对误差(RE)值在-14.8%至11.3%之间;批内和批间变异系数(CV)值分别<8.8%和<10.5%。分析物表现出良好的稳定性,RE值在-13.6%至10.9%之间,CV值<8.9%。此外,使用该方法和传统手动预处理方法测定临床样品中的血浆浓度,结果相似。因此,本研究开发的方法可被认为是患者常规TDM的一种有用的预处理方法。