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采用气相色谱-质谱联用技术对遗传性代谢疾病进行尿液有机酸分析。

Urine organic acid analysis for inherited metabolic disease using gas chromatography-mass spectrometry.

作者信息

Jones Patricia M, Bennett Michael J

机构信息

Department of Pathology, University of Texas Southwestern Medical Center and Children's Medical Center, Dallas, TX, USA.

出版信息

Methods Mol Biol. 2010;603:423-31. doi: 10.1007/978-1-60761-459-3_41.

Abstract

Urine organic acid analysis is an essential component of the workup of the patient suspected to have an inborn error of metabolism (IEM). Urine contains several hundred different organic acids, which arise from a multitude of different sources including both normal and abnormal metabolism. They may also arise from drugs and drug metabolism or from xenobiotics and dietary supplements. In addition to the diagnosis of inborn errors of metabolism, the identification of organic acids in a urine sample has a wide range of potential applications, including toxicology and poisonings. The method described below extracts the acidic fraction from urine samples, derivatizes the extracted compounds, and identifies intermediate metabolites by GC-MS. The method utilizes electron impact ionization gas chromatography-mass spectrometry (GC-MS) with total ion collection.

摘要

尿液有机酸分析是疑似患有先天性代谢缺陷(IEM)患者检查的重要组成部分。尿液中含有数百种不同的有机酸,它们来自多种不同来源,包括正常和异常代谢。它们也可能来自药物及其代谢产物,或来自外源性物质和膳食补充剂。除了用于诊断先天性代谢缺陷外,尿液样本中有机酸的鉴定还有广泛的潜在应用,包括毒理学和中毒方面。以下所述方法从尿液样本中提取酸性成分,对提取的化合物进行衍生化,并通过气相色谱 - 质谱联用(GC-MS)鉴定中间代谢产物。该方法采用具有全离子收集功能的电子轰击电离气相色谱 - 质谱联用仪(GC-MS)。

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