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毛细管电泳-质谱联用测定临床尿液样品中的炎症性肠病药物。

Capillary Electrophoresis Hyphenated with Mass Spectrometry for Determination of Inflammatory Bowel Disease Drugs in Clinical Urine Samples.

机构信息

Department of Pharmaceutical Analysis and Nuclear Pharmacy, Faculty of Pharmacy, Comenius University in Bratislava, Odbojárov 10, SK-832 32 Bratislava, Slovakia.

Toxicological and Antidoping Center (TAC), Faculty of Pharmacy, Comenius University in Bratislava, Odbojárov 10, SK-832 32 Bratislava, Slovakia.

出版信息

Molecules. 2017 Nov 15;22(11):1973. doi: 10.3390/molecules22111973.

Abstract

Azathioprine is the main thiopurine drug used in the treatment of immune-based inflammations of gastrointestinal tract. For the purpose of therapy control and optimization, effective and reliable analytical methods for a rapid drug monitoring in biological fluids are essential. Here, we developed a separation method based on the capillary electrophoresis (CE) hyphenated with tandem mass spectrometry (MS/MS) for the simultaneous determination of azathioprine and its selected metabolites (6-thioguanine, 6-mercaptopurine, and 6-methylmercaptopurine) as well as other co-medicated drugs (mesalazine, prednisone, and allopurinol). The optimized CE-MS/MS conditions provided a very efficient and stable system for the separation and sensitive detection of these drugs in human urine matrices. The developed method was successfully applied for the assay of the targeted drugs and their selected metabolites in urine samples collected from patients suffering from inflammatory bowel disease (IBD) and receiving azathioprine therapy. The developed CE-MS/MS method, due to its reliability, short analysis time, production of complex clinical profiles, and favorable performance parameters, evaluated according to FDA guidelines for bioanalytical method validation, is proposed for routine clinical laboratories to optimize thiopurine therapy, estimate enzymatic activity, and control patient compliance with medication and co-medication.

摘要

硫唑嘌呤是治疗胃肠道免疫性炎症的主要硫嘌呤药物。为了进行治疗控制和优化,在生物体液中进行快速药物监测,需要有效的和可靠的分析方法。在这里,我们开发了一种基于毛细管电泳(CE)与串联质谱(MS/MS)联用的分离方法,用于同时测定硫唑嘌呤及其选定的代谢物(6-硫鸟嘌呤、6-巯基嘌呤和 6-甲基巯基嘌呤)以及其他合并用药(美沙拉嗪、泼尼松和别嘌醇)。优化的 CE-MS/MS 条件为在人尿液基质中分离和灵敏检测这些药物提供了非常高效和稳定的系统。所开发的方法已成功应用于炎症性肠病(IBD)患者接受硫唑嘌呤治疗时收集的尿液样本中目标药物及其选定代谢物的测定。所开发的 CE-MS/MS 方法由于其可靠性、短的分析时间、产生复杂的临床概况以及根据 FDA 生物分析方法验证指南评估的良好性能参数,建议常规临床实验室用于优化硫嘌呤治疗、估计酶活性以及控制患者对药物和合并用药的依从性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/6150202/1a642b500c72/molecules-22-01973-g001.jpg

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