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采用液相色谱-串联质谱法测定正常受试者血浆和尿液中的内源性尿嘧啶和二氢尿嘧啶。

Measurement of endogenous uracil and dihydrouracil in plasma and urine of normal subjects by liquid chromatography-tandem mass spectrometry.

作者信息

Jiang Hao, Jiang Ji, Hu Pei, Hu Yufang

机构信息

Clinical Pharmacology Research Center, Peking Union Medical College Hospital and Chinese Academy of Medical Sciences, Beijing, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Mar 25;769(1):169-76. doi: 10.1016/s1570-0232(02)00009-0.

Abstract

A sensitive and specific HPLC-MS-MS method was developed for the determination of endogenous uracil (Ura) and its metabolite dihydrouracil (UH2) in human plasma and urine samples. Plasma samples were extracted with ethyl acetate-isopropanol (85:15, v/v) following added ammonium sulfate, and then separated on a Discovery Amide C16 column with 3% methanol solution as the mobile phase; urine samples were just centrifuged at 2500 g for detection. Quantitation was carried out by LC-MS-MS in the multiple reaction monitoring (MRM) mode. The limits of quantitation of the method for Ura and UH2 were 0.5 and 5 ng ml(-1) (for plasma), and 50 and 100 ng ml(-1) (for urine), respectively. This method can be useful to evaluate the activity of dihydropyrimidine dehydrogenase (DPD), a rate-limiting enzyme of the chemotherapy drug fluoropyrimidine, which will be helpful in investigating subject variation of DPD and adjusting clinical dosage in pyrimidine chemotherapy.

摘要

建立了一种灵敏且特异的高效液相色谱-串联质谱法,用于测定人血浆和尿液样本中的内源性尿嘧啶(Ura)及其代谢物二氢尿嘧啶(UH2)。血浆样本在加入硫酸铵后用乙酸乙酯-异丙醇(85:15,v/v)萃取,然后在以3%甲醇溶液为流动相的Discovery Amide C16柱上分离;尿液样本仅以2500 g离心后进行检测。通过液相色谱-串联质谱在多反应监测(MRM)模式下进行定量分析。该方法对Ura和UH2的定量限分别为0.5和5 ng/ml(针对血浆),以及50和100 ng/ml(针对尿液)。该方法可用于评估化疗药物氟嘧啶的限速酶二氢嘧啶脱氢酶(DPD)的活性,这将有助于研究DPD的个体差异并在嘧啶化疗中调整临床剂量。

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