An extraction/enzymatic procedure for serum cholesterol measurement: evaluation of performance characteristics.

C Franzini, P Luraschi
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Abstract

The performance characteristics of an extraction/enzymatic procedure for serum cholesterol measurement were evaluated. The procedure is substantially derived from the accepted reference method as standardized by the Centers for Disease Control, substituting the enzymatic reaction for the Liebermann-Burchard reaction. Imprecision (CV) was consistently less than 1.5%, and accuracy was comparable to that of the definitive isotope dilution mass spectrometry method and the accepted reference method. Direct comparison of the enzymatic with the Liebermann-Burchard reaction, using a set of 50 human sera, revealed about -0.05 mmol/l constant bias of the former versus the latter, this being possibly due to higher specificity of the enzymatic reaction. As compared with the accepted reference method, the method described is characterized by higher practicability, the reagent being easier to prepare and to handle, and generating a more stable, chemically defined end-product.

血清胆固醇测定的萃取/酶法:性能特征的评价。
评价了提取/酶法测定血清胆固醇的性能特点。该程序基本上来源于疾病控制中心标准化的公认参考方法,用酶反应代替lieberman - burchard反应。不精密度(CV)始终小于1.5%,准确度与同位素稀释质谱法和公认的参考方法相当。使用一组50人血清,将酶与lieberman - burchard反应直接比较,发现前者与后者的恒定偏差约为-0.05 mmol/l,这可能是由于酶的反应具有更高的特异性。与公认的参考方法相比,所描述的方法具有更高的实用性,试剂更容易制备和处理,并且产生更稳定,化学定义的最终产物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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