Turpeinen U, Koivunen E, Stenman U H
Helsinki University Central Hospital, Department I of Obstetrics and Gynecology, Finland.
Clin Chem. 1987 Oct;33(10):1756-60.
We report a reversed-phase "high-performance" liquid-chromatographic assay for beta 2-microglobulin, alpha 1-acid glycoprotein, and albumin in urine. The urine samples are chromatographed on a 15 X 3.2 mm C18-column with a solvent gradient between two mixtures: 1 mL of trifluoroacetic acid per liter of water and 1 mL of trifluoroacetic acid per liter of acetonitrile. The proteins are detected at 218 nm. The useful lower limit of sensitivity for quantification is 0.1 micrograms of each protein in 100-microliters injected samples, corresponding to 1 mg of protein per liter of urine. The linear measuring range extends from 0.1 to 100 micrograms of protein for each peak. Mean analytical recoveries ranged from 92 to 100%. The mean within-assay CV was 7.5%, the between-assay CV 15%. Comparison of results with those obtained by immunoturbidimetry and radioimmunoassay shows acceptable correlation. Reproducible and rapid with low operational cost, this method is suitable for use in routine screening and quantification of urinary proteins.
我们报告了一种用于尿液中β2-微球蛋白、α1-酸性糖蛋白和白蛋白的反相“高效”液相色谱测定法。尿液样本在一根15×3.2 mm的C18柱上进行色谱分析,使用两种混合物之间的溶剂梯度:每升水含1 mL三氟乙酸和每升乙腈含1 mL三氟乙酸。蛋白质在218 nm处检测。定量的有用灵敏度下限为在100微升进样样本中每种蛋白质0.1微克,相当于每升尿液中1毫克蛋白质。每个峰的线性测量范围从0.1至100微克蛋白质。平均分析回收率在92%至100%之间。批内CV均值为7.5%,批间CV为15%。将结果与通过免疫比浊法和放射免疫测定法获得的结果进行比较,显示出可接受的相关性。该方法可重现、快速且操作成本低,适用于尿液蛋白质的常规筛查和定量。