气相色谱-质谱联用和高效液相色谱分析代谢性胆汁淤积和过氧化物酶体疾病患者血清胆汁酸的优化方法。

F Courillon, M F Gerhardt, A Myara, F Rocchiccioli, F Trivin
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引用次数: 13

摘要

采用气相色谱-质谱联用电子电离法测定了人血清中胆汁酸为甲酯-三甲基硅醚。对整个方法进行了验证,检出限为0.4 μ mol/l,线性度为2 ~ 30 μ mol/l,日内、日间精密度、准确度和回收率为96.2%(以不-23-去氧胆酸为内标)。采用气相色谱-质谱法和高效液相色谱法测定43例胆汁淤积症患者血清c24 -胆汁酸谱。两种方法的结果具有良好的相关性,确定了HPLC和GC-MS的选择标准。同时,采用气相色谱-质谱法测定了广泛性过氧化物酶体缺乏症(如Zellweger综合征(n = 5)、新生儿肾上腺白质营养不良(n = 1)、婴儿Refsum病(n = 2)和单一过氧化物酶体缺乏症(n = 1)患者的血清C24-和c27 -胆汁酸和C29二羧酸谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The optimized use of gas chromatography-mass spectrometry and high performance liquid chromatography to analyse the serum bile acids of patients with metabolic cholestasis and peroxisomal disorders.

We have measured the bile acids in human serum as methyl ester-trimethylsilyl ethers by gas chromatography-mass spectrometry (GC-MS) using an electron ionization procedure. The overall method was validated and the detection limit (0.4 mumol/l), linearity (2-30 mumol/l), intra-day and inter-day precision, accuracy and recovery (96.2% for nor-23-deoxycholic acid as internal standard) were measured. Serum C24-bile acids profiles from 43 cholestatic patients were measured by GC-MS and by HPLC. The results obtained with the two methods were well correlated and the criteria for selecting either HPLC or GC-MS identified. The serum C24- and C27-bile acids and C29 dicarboxylic bile acid profiles for patients with generalized peroxisomal deficiencies, like Zellweger syndrome (n = 5), neonatal adrenoleukodystrophy (n = 1), infantile Refsum disease (n = 2) and from a single peroxisomal deficiency (n = 1) were also measured by GC-MS.

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