首页> 美国卫生研究院文献>International Journal of Analytical Chemistry >Development and Validation of a Simple High Performance Liquid Chromatography/UV Method for Simultaneous Determination of Urinary Uric Acid Hypoxanthine and Creatinine in Human Urine
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Development and Validation of a Simple High Performance Liquid Chromatography/UV Method for Simultaneous Determination of Urinary Uric Acid Hypoxanthine and Creatinine in Human Urine

机译:同时测定人尿中尿酸次黄嘌呤和肌酐的简单高效液相色谱/紫外方法的开发与验证

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摘要

Uric acid and hypoxanthine are produced in the catabolism of purine. Abnormal urinary levels of these products are associated with many diseases and therefore it is necessary to have a simple and rapid method to detect them. Hence, we report a simple reverse phase high performance liquid chromatography (HPLC/UV) technique, developed and validated for simultaneous analysis of uric acid, hypoxanthine, and creatinine in human urine. Urine was diluted appropriately and eluted with C-18 column 100 mm × 4.6 mm with a C-18 precolumn 25 mm × 4.6 mm in series. Potassium phosphate buffer (20 mM, pH 7.25) at a flow rate of 0.40 mL/min was employed as the solvent and peaks were detected at 235 nm. Tyrosine was used as the internal standard. The experimental conditions offered a good separation of analytes without interference of endogenous substances. The calibration curves were linear for all test compounds with a regression coefficient, r2 > 0.99. Uric acid, creatinine, tyrosine, and hypoxanthine were eluted at 5.2, 6.1, 7.2, and 8.3 min, respectively. Intraday and interday variability were less than 4.6% for all the analytes investigated and the recovery ranged from 98 to 102%. The proposed HPLC procedure is a simple, rapid, and low cost method with high accuracy with minimum use of organic solvents. This method was successfully applied for the determination of creatinine, hypoxanthine, and uric acid in human urine.
机译:尿酸和次黄嘌呤是嘌呤的分解代谢产物。这些产品的尿液异常水平与许多疾病有关,因此有必要采用一种简单而快速的方法来检测它们。因此,我们报告了一种简单的反相高效液相色谱(HPLC / UV)技术,该技术已开发并验证用于同时分析人尿中的尿酸,次黄嘌呤和肌酐。尿液经适当稀释后,用C-18色谱柱100 mm×4.6 mm洗脱,串联C-18预柱25 mm×4.6 mm。磷酸钾缓冲液(20?mM,pH 7.25)以0.40?mL / min的流速用作溶剂,并在235?nm处检测到峰。酪氨酸用作内标。实验条件提供了良好的分析物分离效果,而没有内源性物质的干扰。所有测试化合物的校准曲线均为线性,回归系数为r 2

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