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用于筛查胱氨酸尿症患者及鉴定胱氨酸结石的液相色谱-质谱分析

Liquid chromatographic-mass spectrometric analysis for screening of patients with cystinuria, and identification of cystine stone.

作者信息

Watanabe H, Sugahara K, Inoue K, Fujita Y, Kodama H

机构信息

Department of Urology, Kochi Medical School, Japan.

出版信息

J Chromatogr. 1991 Aug 23;568(2):445-50. doi: 10.1016/0378-4347(91)80182-c.

DOI:10.1016/0378-4347(91)80182-c
PMID:1783649
Abstract

Analyses of amino acids in the urine of a normal human and of patients with heterozygous and homozygous cystinuria have been carried out, using liquid chromatography-mass spectrometry with an atmospheric pressure ionization interface system. A kidney cystine stone was also analysed by this system. Very intense quasi-molecular ions ([M + H]+) of standard cystine, arginine, lysine and ornithine were observed on mass chromatograms as base peaks. Mass chromatograms of the urine samples from a normal human and from patients with heterozygous and homozygous cystinuria were easily distinguishable. The retention times in the mass chromatogram and mass spectrum of kidney stone cystine was almost the same as that of authentic cystine.

摘要

利用带有大气压电离接口系统的液相色谱 - 质谱联用技术,对正常人和杂合子及纯合子胱氨酸尿症患者的尿液中的氨基酸进行了分析。还用该系统对一块肾胱氨酸结石进行了分析。在质量色谱图上,标准胱氨酸、精氨酸、赖氨酸和鸟氨酸的非常强的准分子离子([M + H]+)作为基峰被观测到。来自正常人以及杂合子和纯合子胱氨酸尿症患者的尿液样本的质量色谱图很容易区分。肾结石胱氨酸在质量色谱图和质谱中的保留时间与纯胱氨酸几乎相同。

相似文献

1
Liquid chromatographic-mass spectrometric analysis for screening of patients with cystinuria, and identification of cystine stone.用于筛查胱氨酸尿症患者及鉴定胱氨酸结石的液相色谱-质谱分析
J Chromatogr. 1991 Aug 23;568(2):445-50. doi: 10.1016/0378-4347(91)80182-c.
2
Diagnostic and genetic studies in 43 patients with classic cystinuria.对43例典型胱氨酸尿症患者的诊断和遗传学研究。
Clin Chem. 1991 Jan;37(1):68-73.
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Reference values of urinary excretion of cystine and dibasic aminoacids: classification of patients with cystinuria in the Valencian Community, Spain.胱氨酸和二元氨基酸尿排泄的参考值:西班牙巴伦西亚自治区胱氨酸尿症患者的分类
Clin Biochem. 1999 Feb;32(1):25-30. doi: 10.1016/s0009-9120(98)00087-3.
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Cystinuria.胱氨酸尿症
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Cystinuria phenotyping by oral lysine and arginine loading.通过口服赖氨酸和精氨酸负荷进行胱氨酸尿症表型分析。
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Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds.胱氨酸尿症患者使用巯基化合物治疗时,总胱氨酸以及二元氨基酸精氨酸、赖氨酸和鸟氨酸的尿排泄量与基因检测结果的关系。
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[Cystine as a risk factor of the stone formation in kidney: the reference value range of urinary excretion, the stage diagnosis of cystine metabolism disorder].[胱氨酸作为肾结石形成的危险因素:尿排泄的参考值范围,胱氨酸代谢紊乱的分期诊断]
Urologiia. 2016 Aug(4):10-14.
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Heterozygous cystinuria and urinary lithiasis.杂合性胱氨酸尿症与尿路结石
Am J Med Genet. 1985 Dec;22(4):703-15. doi: 10.1002/ajmg.1320220407.
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Biochemical and genetic studies in cystinuria: observations on double heterozygotes of genotype I-II.胱氨酸尿症的生化与遗传学研究:关于I-II型双杂合子的观察
J Clin Invest. 1971 Sep;50(9):1961-76. doi: 10.1172/JCI106688.
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Cystinuria: a new genetic variant.胱氨酸尿症:一种新的基因变体。
Clin Sci Mol Med. 1976 Jul;51(1):27-32. doi: 10.1042/cs0510027.