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通过琼脂糖凝胶电泳和酶法胆固醇染色对高密度、低密度和极低密度脂蛋白以及脂蛋白(a)进行定量测定。

Quantitative determination of high-, low-, and very-low-density lipoproteins and lipoprotein(a) by agarose gel electrophoresis and enzymatic cholesterol staining.

作者信息

Nauck M, Winkler K, März W, Wieland H

机构信息

Department of Medicine, University Hospital of Freiburg, Germany.

出版信息

Clin Chem. 1995 Dec;41(12 Pt 1):1761-7.

PMID:7497617
Abstract

Quantification of lipoprotein cholesterol was performed by enzymatic staining of cholesterol in a new agarose gel electrophoresis method that allows the separation of LDL, VLDL, HDL, and lipoprotein(a) [Lp(a)]. Lp(a) shows an electrophoretic mobility clearly distinct from VLDL and HDL. The total CVs of lipoprotein cholesterol varied between 2.7% and 3.9% for LDL, 7.8% and 23.2% for VLDL, 5.2% and 9.5% for HDL, and 6.8% and 16.4% for Lp(a). Comparison of LDL-, VLDL-, and HDL-cholesterol concentrations with the results of a combined ultracentrifugation and precipitation technique gave correlation coefficients of 0.961, 0.947, and 0.918, respectively; comparison of Lp(a)-cholesterol values with those of a nephelometric Lp(a) assay gave r = 0.906. The new electrophoretic assay has several advantages: It allows the quantification of Lp(a)-cholesterol; VLDL-cholesterol is not affected by Lp(a)-cholesterol; and the LDL-cholesterol fraction does not contain Lp(a)-cholesterol, as happens with LDL-cholesterol determined by ultracentrifugation and precipitation.

摘要

采用一种新的琼脂糖凝胶电泳法,通过对胆固醇进行酶染色来定量脂蛋白胆固醇,该方法可分离低密度脂蛋白(LDL)、极低密度脂蛋白(VLDL)、高密度脂蛋白(HDL)和脂蛋白(a)[Lp(a)]。Lp(a)的电泳迁移率明显不同于VLDL和HDL。脂蛋白胆固醇的总变异系数在LDL为2.7%至3.9%、VLDL为7.8%至23.2%、HDL为5.2%至9.5%、Lp(a)为6.8%至16.4%之间。将LDL、VLDL和HDL胆固醇浓度与超速离心和沉淀联合技术的结果进行比较,相关系数分别为0.961、0.947和0.918;将Lp(a)胆固醇值与散射比浊法测定的Lp(a)值进行比较,r = 0.906。这种新的电泳测定法有几个优点:它可对Lp(a)胆固醇进行定量;VLDL胆固醇不受Lp(a)胆固醇影响;LDL胆固醇组分不含Lp(a)胆固醇,而超速离心和沉淀法测定的LDL胆固醇则会出现这种情况。

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