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使用自动预处理液相色谱/串联质谱系统进行治疗药物监测的同步药物浓度测量方法的开发

Development of Simultaneous Drug Concentration Measurement Method Using an Automated Pretreatment Liquid Chromatography/Tandem Mass Spectrometry System for Therapeutic Drug Monitoring.

作者信息

Sato Yu, Kondo Hiroki, Sato Yuji, Abe Ai, Kikuchi Masafumi, Sato Toshihiro, Kumondai Masaki, Yoshikawa Kohei, Hayakawa Yoshihiro, Maekawa Masamitsu, Mano Nariyasu

机构信息

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.

出版信息

Pharmaceutics. 2024 Aug 28;16(9):1138. doi: 10.3390/pharmaceutics16091138.

DOI:10.3390/pharmaceutics16091138
PMID:39339175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11435224/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/71877ed5c280/pharmaceutics-16-01138-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/7781e0786e65/pharmaceutics-16-01138-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/a35f5bd05b41/pharmaceutics-16-01138-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/23049bbe3bb3/pharmaceutics-16-01138-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/475b7040fefb/pharmaceutics-16-01138-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/796f78bfdf16/pharmaceutics-16-01138-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/71877ed5c280/pharmaceutics-16-01138-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/7781e0786e65/pharmaceutics-16-01138-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/a35f5bd05b41/pharmaceutics-16-01138-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/23049bbe3bb3/pharmaceutics-16-01138-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/475b7040fefb/pharmaceutics-16-01138-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/796f78bfdf16/pharmaceutics-16-01138-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae22/11435224/71877ed5c280/pharmaceutics-16-01138-g006.jpg

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