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使用一种灵敏试剂和Cobas Bio离心分析仪对高密度脂蛋白磷脂进行酶法测定。

Enzymatic determination of high density lipoprotein phospholipid using a sensitive reagent and a Cobas Bio Centrifugal Analyzer.

作者信息

Moshides J S

机构信息

Department of Clinical Chemistry, Prince of Wales Hospital, Sydney, Australia.

出版信息

Scand J Clin Lab Invest. 1988 Feb;48(1):59-64. doi: 10.3109/00365518809085394.

Abstract

A sensitive enzymatic method for the measurement of high density lipoprotein choline-containing phospholipids (HDL-pc) was adapted to a Cobas Bio Centrifugal Analyzer. The Boehringer Mannheim phospholipase D/choline oxidase/peroxidase reagent was modified by the inclusion of 2,4,6,-tribromo-3-hydroxybenzoic acid (TBHBA) which reacts with hydrogen peroxide and 4-aminophenazone to produce a quinone-imine dye with a fourfold greater molar absorption than that produced with phenol. The method has been developed for the determination of HDL fractions isolated with polyethylene glycol 6000, for which a reagent of high sensitivity is required. The method is linear to 5.5 mmol/l of HDL-pc and the CVs for within-run and day-to-day imprecision were less than 3.5%. Correlation of HDL cholesterol (HDL-c) with HDL-pc values in 200 healthy subjects was good (r = 0.9024). The mean (+/- SD) HDL-pc value for men was 1.12 (+/- 0.26) and for women, 1.34 (+/- 0.29) mmol/l. The assay is inexpensive and large numbers of specimens can be processed rapidly and conveniently.

摘要

一种用于测量高密度脂蛋白含胆碱磷脂(HDL-pc)的灵敏酶法被应用于Cobas Bio离心分析仪。通过加入2,4,6-三溴-3-羟基苯甲酸(TBHBA)对勃林格殷格翰磷脂酶D/胆碱氧化酶/过氧化物酶试剂进行了改进,该物质与过氧化氢和4-氨基苯并酮反应生成一种醌亚胺染料,其摩尔吸光率是苯酚产生的染料的四倍。该方法是为测定用聚乙二醇6000分离的HDL组分而开发的,为此需要一种高灵敏度的试剂。该方法对HDL-pc在5.5 mmol/l范围内呈线性,批内和批间不精密度的变异系数(CV)小于3.5%。200名健康受试者的HDL胆固醇(HDL-c)与HDL-pc值的相关性良好(r = 0.9024)。男性的平均(±标准差)HDL-pc值为1.12(±0.26)mmol/l,女性为1.34(±0.29)mmol/l。该检测方法成本低廉,可快速、方便地处理大量标本。

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