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高效液相色谱法测定尿液中6-N-三甲基赖氨酸

Determination of 6-N-trimethyllysine in urine by high-performance liquid chromatography.

作者信息

Hoppel C L, Weir D E, Gibbons A P, Ingalls S T, Brittain A T, Brown F M

出版信息

J Chromatogr. 1983 Jan 14;272(1):43-50. doi: 10.1016/s0378-4347(00)86101-0.

Abstract

A method for determination of 6-N-trimethyllysine in urine is described. Trimethyllysine and the chemically analogous 6-N-triethyllysine internal standard were isolated from aqueous samples by microcolumn ion-exclusion chromatography. The specimens were derivatized by reaction with 1-fluoro-2,4-dinitrobenzene and reaction byproducts extracted by organic solvents. The trimethyllysine and internal standard derivatives were separated easily from other sample constituents by reversed-phase paired-ion high-performance liquid chromatography with spectrophotometric detection at 405 nm. Standard curves were linear over a sample concentration range of 10-150 nmol/ml; the detection limit corresponded with 0.1 nmol trimethyllysine injected into the chromatograph. The procedure was used for determination of trimethyllysine in human urine.

摘要

本文描述了一种测定尿中6-N-三甲基赖氨酸的方法。通过微柱离子排斥色谱法从水性样品中分离出三甲基赖氨酸和化学类似物6-N-三乙基赖氨酸内标。样品通过与1-氟-2,4-二硝基苯反应进行衍生化,并用有机溶剂萃取反应副产物。通过反相配对离子高效液相色谱法在405nm处进行分光光度检测,可轻松将三甲基赖氨酸和内标衍生物与其他样品成分分离。标准曲线在10-150nmol/ml的样品浓度范围内呈线性;检测限对应于注入色谱仪的0.1nmol三甲基赖氨酸。该方法用于测定人尿中的三甲基赖氨酸。

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