Kupke I R
J Clin Chem Clin Biochem. 1976 May;14(5):217-23. doi: 10.1515/cclm.1976.14.1-12.217.
A new method for the quantitative determination of the cholesterol content of serum lipoprotein is described. Electrophoresis of the serum lipoproteins on agarose gel is followed by the enzymatic determination of the lipoprotein cholesterol. The cholesterol is released from the agarose pieces containing the lipoproteins by dissolving the agarose with HCl. No influence of the HCl on cholesterol, and no influence of the agarose degradation products on the enzyme reactions was observed. The analytical procedure is simple and only 20 mul serum are required. The average coefficient of variation for the determination of the beta-lipoprotein cholesterol less than 4%, and it is less than 8% in the pre-beta-lipoproteins of Type IV hyperlipidemic patients. The cholesterol contents found in the other lipoprotein fractions have to be interpreted as an approximation. Semiautomation seems to be possible. In preliminary studies, the cholesterol concentrations of the serum lipoproteins were determined in some control subjects and some hyperlipidemic patients. The results are in good agreement with data obtained by ultracentrifuge studies performed by other investigators. The advangates of this new procedure and aspects of application are discussed.
本文描述了一种定量测定血清脂蛋白胆固醇含量的新方法。血清脂蛋白在琼脂糖凝胶上进行电泳,然后对脂蛋白胆固醇进行酶法测定。通过用盐酸溶解含脂蛋白的琼脂糖块,使胆固醇从琼脂糖块中释放出来。未观察到盐酸对胆固醇有影响,也未观察到琼脂糖降解产物对酶反应有影响。分析过程简单,仅需20微升血清。测定β-脂蛋白胆固醇的平均变异系数小于4%,在IV型高脂血症患者的前β-脂蛋白中小于8%。在其他脂蛋白组分中发现的胆固醇含量只能作为近似值来解释。半自动化似乎是可行的。在初步研究中,测定了一些对照受试者和一些高脂血症患者血清脂蛋白的胆固醇浓度。结果与其他研究者通过超速离心研究获得的数据高度一致。本文讨论了这一新方法的优点及应用方面。