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采用液相色谱-电喷雾串联质谱法同时测定人血浆和尿液中的对乙酰氨基酚及其葡萄糖醛酸结合物:在临床药代动力学研究中的应用。

Simultaneous quantitative determination of paracetamol and its glucuronide conjugate in human plasma and urine by liquid chromatography coupled to electrospray tandem mass spectrometry: application to a clinical pharmacokinetic study.

机构信息

The Clinical Pharmacy & Pharmacology Research Institute, The Second Xiangya Hospital, Central South University, Changsha 410011, People's Republic of China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Apr 15;893-894:162-7. doi: 10.1016/j.jchromb.2012.02.027. Epub 2012 Feb 23.

DOI:10.1016/j.jchromb.2012.02.027
PMID:22445307
Abstract

A specific, sensitive and rapid method based on high performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS) was developed for the simultaneous determination of paracetamol (APAP) and its glucuronide conjugate (PG) in human plasma and urine. Plasma samples were precipitated with the mixture of acetonitrile and propylene glycol (90:10, v/v) solution and urine samples were diluted with the mobile phase, which were used to isolate the analytes from biological matrices followed by injection of the extracts onto a C(18) column with isocratic elution. Detection was carried out on a triple quadrupole tandem mass spectrometer in multiple reaction monitoring (MRM) mode using positive electrospray ionization (ESI(+)). The method was validated over the concentration range of 10-30,000 ng/mL and 100-6000 ng/mL for APAP in human plasma and urine as well as 10-15,000 ng/mL and 200-60,000 ng/mL for PG in human plasma and urine, respectively. Inter- and intra-run precisions of APAP and PG were less than 15% and the accuracy was within 85-115% for both plasma and urine. The average extraction recoveries were 93.1% and 89.1% for APAP, and 93.7% and 92.3% for PG in human plasma and urine, respectively. The linearity, recovery and stability were validated for APAP and PG in human plasma and urine. The method proved to be simple, robust and time efficient.

摘要

建立了一种基于高效液相色谱-串联质谱(HPLC-MS/MS)的特异、灵敏、快速的方法,用于同时测定人血浆和尿液中的扑热息痛(APAP)及其葡萄糖醛酸缀合物(PG)。血浆样品用乙腈和丙二醇(90:10,v/v)溶液沉淀,尿液样品用流动相稀释,用于从生物基质中分离分析物,然后将提取物注入 C(18)柱,采用等度洗脱。采用正电喷雾电离(ESI(+))在多重反应监测(MRM)模式下,在三重四极杆串联质谱仪上进行检测。该方法在人血浆和尿液中 APAP 的浓度范围为 10-30000ng/mL 和 100-6000ng/mL,在人血浆和尿液中 PG 的浓度范围为 10-15000ng/mL 和 200-60000ng/mL 时进行了验证。APAP 和 PG 的日内和日间精密度均小于 15%,准确度在血浆和尿液中均为 85-115%。APAP 在人血浆和尿液中的平均提取回收率分别为 93.1%和 89.1%,PG 的平均提取回收率分别为 93.7%和 92.3%。对人血浆和尿液中的 APAP 和 PG 进行了线性、回收率和稳定性验证。该方法简单、稳健、高效。

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