Suppr超能文献

采用液相色谱-串联质谱法测定人血浆中的芬太尼以及人尿液中的芬太尼和去甲芬太尼。

Determination of fentanyl in human plasma and fentanyl and norfentanyl in human urine using LC-MS/MS.

作者信息

Huynh N-H, Tyrefors N, Ekman L, Johansson M

机构信息

Quintiles AB, Analytical Services, Strandbodgatan 1, SE 75323 Uppsala, Sweden.

出版信息

J Pharm Biomed Anal. 2005 Apr 29;37(5):1095-100. doi: 10.1016/j.jpba.2004.09.024.

Abstract

Fentanyl, a potent analgesic drug, has traditionally been used intravenously in surgical or diagnostic operations. Formulations with fentanyl in oral transmucosal delivery system and in transdermal depot-patch have also been developed against breakthrough pain in cancer patients. In this report, LC-MS/MS methods to determine fentanyl in human plasma as well as fentanyl and its main metabolite, norfentanyl, in human urine are presented together with validation data. The validation ranges were 0.020-10.0 and 0.100-50.0 ng/ml for fentanyl in plasma and urine, respectively, and 0.102-153 ng/ml for norfentanyl in urine. Liquid-liquid extraction of the compounds fentanyl, norfentanyl and the deuterated internal standards, fentanyl-d5 and norfentanyl-d5 from the matrixes was applied and separation was performed on a reversed phase YMC Pro C18-column followed by MS/MS detection with electrospray in positive mode. The inter-assay precision (CV%) was better than 4.8% for fentanyl in plasma and 6.2% and 4.7% for fentanyl and norfentanyl, respectively, in urine. The ruggedness of the methods, selectivity, recovery, effect of dilution and long-term stability of the analytes in plasma and urine were investigated. Effect of haemolysis and stability of fentanyl in blood samples were also studied. The methods have been applied for the determination of fentanyl in plasma samples and fentanyl/norfentanyl in urine samples taken for pharmacokinetic evaluation after a single intra-venous (i.v.) dose of 75 microg fentanyl.

摘要

芬太尼是一种强效镇痛药,传统上用于外科手术或诊断操作中的静脉给药。还开发了口服黏膜给药系统和透皮长效贴剂等含芬太尼的制剂,用于缓解癌症患者的爆发性疼痛。在本报告中,介绍了用于测定人血浆中芬太尼以及人尿液中芬太尼及其主要代谢物去甲芬太尼的液相色谱-串联质谱(LC-MS/MS)方法及验证数据。血浆和尿液中芬太尼的验证范围分别为0.020 - 10.0 ng/ml和0.100 - 50.0 ng/ml,尿液中去甲芬太尼的验证范围为0.102 - 153 ng/ml。采用液-液萃取法从基质中提取芬太尼、去甲芬太尼以及氘代内标物芬太尼-d5和去甲芬太尼-d5,并在反相YMC Pro C18柱上进行分离,随后采用电喷雾正离子模式进行串联质谱检测。血浆中芬太尼的批间精密度(CV%)优于4.8%,尿液中芬太尼和去甲芬太尼的批间精密度分别为6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验