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机构地区:[1]南昌大学分析测试中心,江西南昌330047 [2]南昌大学食品科学与技术国家重点实验室,江西南昌330047
出 处:《分析科学学报》2009年第4期405-408,共4页Journal of Analytical Science
基 金:国家自然科学基金(No.20765002);江西省自然科学基金(No.0620049)
摘 要:建立了人体尿液中蝶呤-6-羧酸的高效液相色谱-紫外分析新方法。运用Lichrospher C18柱(250×4.6mm,5μm),甲醇-水(70:30,V/V)为流动相,流速为0.4mL/min,可较好地将尿液中蝶呤-6-羧酸与其它共存干扰物质分离。在355nm检测波长下,蝶呤-6-羧酸在0.19~4.8μg/mL范围内与色谱峰面积呈良好线性关系,相关系数为0.9999,方法检出限为0.015μg/mL。尿液经0.45μm滤膜过滤后,可直接进样分析,方法简便,应用于癌症病人和健康人尿样中蝶呤-6-羧酸测定,结果较好。方法的加标回收率为94.6%~100.2%,相对标准偏差为0.81%~5.07%。A new method based on high-performance liquid chromatography-ultraviolet detection was established for the determination of pterin-6-carboxylic acid in human urine. After filtrated, urine samples were directly separated on a Lichrospher C18 column by using methanol-water (70: 30 ,V/V) as mobile phase, at the flow rate of 0.4 mL/min and the detection wavelength of 355 nm. The proposed method has successfully applied to the determination of the content of pterin-6-carboxylic acid in both healthy human urine and the cancer patients ' urine samples. The intensity of absorbance was proportional to the concentration of pterin-6-carboxylic acid over the range of 0.19-4.8 μg/mL, with the linear correlation coefficient of 0. 9999. The average recoveries were between 94.6% and 100.2%, and the relative standard deviation was less than 5.07 %.
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