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Determination of Epidermal Growth Factors in Human Urine by High Performance Liquid Chromatography Using Anti-hEGF Antibody Precolumn

机译:抗hEGF抗体前柱的高效液相色谱法测定人尿中的表皮生长因子

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A high performance liquid chromatographic method for the determination of human epidermal growth factors (hEGFs) in human urine is described. Using an anti-hEGF antibody column as a precolumn and an ODS column as an analytical column, each urine sample was directly injected onto the precolumn with aqueous mobile phase. With 0.2% trichloroacetic acid solution, the trapped hEGFs were transferred to the analytical column to allow their separation by reversed phase mode. The present method revealed that human urine contains hEGF[1-50], [1-51] and [1-52] in addition to hEGF[1-53]; the content determined by native fluorescence detection coincided with that by enzyme immunoassay. In the present method, the relative standard deviation (RSD) was less than 3% (n=6) for 25ng/ml of hEGF[1-53] and the detection limit was ca. 3ng for each hEGF, and the loading capacity of hEGF[1-53] on the anti-hEGF antibody precolumn was unchanged during analyses of 500 human urine samples.
机译:描述了一种用于测定人尿中人表皮生长因子(hEGFs)的高效液相色谱方法。使用抗hEGF抗体柱作为预柱,使用ODS柱作为分析柱,将每个尿液样品直接注入具有水相流动相的预柱中。用0.2%的三氯乙酸溶液,将捕获的hEGF转移到分析柱中,以反相模式进行分离。本方法揭示了人尿除了hEGF [1-53]外还含有hEGF [1-50],[1-51]和[1-52]。通过天然荧光检测测定的含量与通过酶免疫测定测定的含量一致。在本方法中,对于25ng / ml的hEGF [1-53],相对标准偏差(RSD)小于3%(n = 6),检出限为。每个hEGF的浓度为3ng,在分析500个人类尿液样品中,hEGF [1-53]在抗hEGF抗体前柱上的负载量没有变化。

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