首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Rapid, hydrolysis-free, dilute-and-shoot method for the determination of buprenorphine, norbuprenorphine and their glucuronides in urine samples using UHPLC-MS/MS
【24h】

Rapid, hydrolysis-free, dilute-and-shoot method for the determination of buprenorphine, norbuprenorphine and their glucuronides in urine samples using UHPLC-MS/MS

机译:使用UHPLC-MS / MS测定尿液样品中丁丙诺啡,Norbuhenorphine和它们的葡糖苷酸的快速,水解,稀释和脱落方法

获取原文
获取原文并翻译 | 示例
           

摘要

Buprenorphine and its metabolites are routinely monitored to assess patient compliance with drug detoxification programs or as pain killers. A rapid method for the simultaneous analysis of buprenorphine, norbuprenorphine, and glucuronides in urine using ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) was developed. Urine samples were diluted in water containing formic acid 0.1% and directly injected into the UHPLC-MS/MS system without any sample pretreatment. Quality control (QC) samples, prepared using 20 different urine matrices, fortified at 3 concentration levels, were quantified using four deuterated internal standards. The accuracy values obtained spanned from 90 to 114% with repeatability lower than 10% also in the inter-day between batch experiments. Matrix effects (ME), evaluated before correction with internal standards using Matuszewski procedure, mainly affected the analysis of buprenorphine glucuronide. The use of deuterated internal standards (IS) for each analyte was necessary to compensate for ME and was essential in the determination of glucuronides. The method was applied to 30 real urine samples from patients under a detoxification therapy. Duplicate analyses were performed with the presented method and compared with another method which involves a standard hydrolysis procedure. Real sample results were compared showing a good performance agreement, with differences between the two methods lower than +/- 20% in the quantification results. (C) 2019 Elsevier B.V. All rights reserved.
机译:常规监测丁丙诺啡及其代谢物,以评估患者遵守药物解毒计划或止痛药。利用超高效液相色谱 - 串联质谱(UHPLC-MS / MS)发育尿丙啡卟啉,非苯甲酰苯和葡糖苷糖苷同时分析尿嘧啶,Norbupernerphines和葡糖尿病的快速方法。尿液样品在含甲酸0.1%的水中稀释,并直接注入UHPLC-MS / MS系统,没有任何样品预处理。使用四种氘代内标进行量化使用20种不同的尿基质制备的质量控制(QC)样品。在批量实验之间的日期间,在90%至114%中截止了90%至114%的常规值。矩阵效应(ME),评估使用Matuszewski程序的内部标准进行校正,主要影响丁丙诺氨酸葡萄糖醛酸的分析。对于每种分析物的使用氘代内标(IS)是为了弥补我,并且在测定葡糖苷糖苷中是必不可少的。在排毒治疗下,将该方法应用于来自患者的30个真正的尿液样本。用呈现的方法进行重复分析,并与涉及标准水解方法的另一种方法进行比较。比较实际样品结果显示出良好的性能协议,两种方法之间的差异在量化结果中低于+/- 20%。 (c)2019 Elsevier B.v.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号