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脂肪酸β-氧化障碍中血浆游离脂肪酸及其3-羟基类似物的同步分析

Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid beta-oxidation disorders.

作者信息

Costa C G, Dorland L, Holwerda U, de Almeida I T, Poll-The B T, Jakobs C, Duran M

机构信息

Centro de Metabolismos e Genética, University of Lisboa, Portugal.

出版信息

Clin Chem. 1998 Mar;44(3):463-71.

PMID:9510849
Abstract

We present a new derivatization procedure for the simultaneous gas chromatographic-mass spectrometric analysis of free fatty acids and 3-hydroxyfatty acids in plasma. Derivatization of target compounds involved trifluoroacetylation of hydroxyl groups and tert-butyldimethylsilylation of the carboxyl groups. This new derivatization procedure had the advantage of allowing the complete baseline separation of free fatty acids and 3-hydroxyfatty acids while the superior gas chromatographic and mass spectrometric properties of tert-butyldimethylsilyl derivatives remained unchanged, permitting a sensitive analysis of the target compounds. Thirty-nine plasma samples from control subjects and patients with known defects of mitochondrial fatty acid beta-oxidation were analyzed. A characteristic increase of long-chain 3-hydroxyfatty acids was observed for all of the long-chain 3-hydroxyacyl-CoA dehydrogenase-deficient and mitochondrial trifunctional protein-deficient plasma samples. For medium-chain acyl-CoA dehydrogenase deficiency and very-long-chain acyl-CoA dehydrogenase deficiency, decenoic and tetradecenoic acids, respectively, were the main abnormal fatty acids, whereas the multiple acyl-CoA dehydrogenase-deficient patients showed variable increases of these unusual intermediates. The results showed that this selective and sensitive method is a powerful tool in the diagnosis and monitoring of mitochondrial fatty acid beta-oxidation disorders.

摘要

我们提出了一种新的衍生化方法,用于同时气相色谱 - 质谱分析血浆中的游离脂肪酸和3 - 羟基脂肪酸。目标化合物的衍生化包括羟基的三氟乙酰化和羧基的叔丁基二甲基硅烷基化。这种新的衍生化方法的优点是能够实现游离脂肪酸和3 - 羟基脂肪酸的完全基线分离,同时叔丁基二甲基硅烷基衍生物优异的气相色谱和质谱特性保持不变,从而能够对目标化合物进行灵敏分析。对来自对照受试者和已知线粒体脂肪酸β氧化缺陷患者的39份血浆样本进行了分析。在所有长链3 - 羟基酰基辅酶A脱氢酶缺乏和线粒体三功能蛋白缺乏的血浆样本中,均观察到长链3 - 羟基脂肪酸有特征性增加。对于中链酰基辅酶A脱氢酶缺乏症和极长链酰基辅酶A脱氢酶缺乏症,癸烯酸和十四碳烯酸分别是主要的异常脂肪酸,而多种酰基辅酶A脱氢酶缺乏的患者则显示出这些异常中间体的不同程度增加。结果表明,这种选择性和灵敏的方法是诊断和监测线粒体脂肪酸β氧化障碍的有力工具。

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