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一种新颖而精确的超速离心和高效液相色谱法同时测定血清高密度脂蛋白和低密度脂蛋白亚组分及脂蛋白(a)胆固醇的方法。

A novel and precise method for simultaneous measurement of serum HDL and LDL subfractions and lipoprotein (a) cholesterol by ultracentrifugation and high-performance liquid chromatography.

机构信息

The Key Laboratory of Geriatrics, Beijing Hospital & Beijing Institute of Geriatrics, Ministry of Health, Beijing, China.

出版信息

Clin Chim Acta. 2012 Jul 11;413(13-14):1071-6. doi: 10.1016/j.cca.2012.02.022. Epub 2012 Mar 3.

DOI:10.1016/j.cca.2012.02.022
PMID:22406178
Abstract

BACKGROUND

We developed an ultracentrifugation and high-performance liquid chromatography (HPLC) method for simultaneous measurement of cholesterol in serum high density lipoprotein (HDL) and low density lipoprotein (LDL) subfractions and lipoprotein (a) [Lp(a)].

METHODS

Serum aliquots of 0.05 ml were centrifuged at background densities of 1.006, 1.044 kg/l, and in the presence of β-mercaptoethanol (ME) at background densities of 1.044, 1.063 and 1.125 kg/l for the separation of lipoprotein subfractions and Lp(a). Cholesterol levels in the ultracentrifugal bottom fractions were analyzed by HPLC.

RESULTS

ME effectively dissociated Lp(a) into apolipoprotein (a) and Lp(a) remnant [Lp(a-)]. Lp(a-) showed a distinctive density distribution from that of the native Lp(a). Based on these data, a method was developed to separate lipoprotein into subfractions and Lp(a) by ultracentrifugation. The separated HDL and LDL subfractions were not contaminated with Lp(a). This method is highly precise with the total CVs for the measurement of HDL2-C, HDL3-C, LDLa-C, LDLb-C and Lp(a)-C 0.85%-2.66%, 0.87%-3.21%, 0.86%-1.11%, 2.59%-6.35% and 4.42%-12.29%, respectively.

CONCLUSION

A new method for the separation of HDL and LDL subfractions and Lp(a) and simultaneous measurement of cholesterol by ultracentrifugation and HPLC have been established. It is precise and sensitive and can be used in research or clinical laboratories for lipoprotein profiling.

摘要

背景

我们开发了一种超速离心和高效液相色谱(HPLC)方法,用于同时测量血清高密度脂蛋白(HDL)和低密度脂蛋白(LDL)亚组分以及脂蛋白(a)[Lp(a)]中的胆固醇。

方法

将 0.05ml 的血清等分试样在 1.006、1.044kg/L 的背景密度下离心,并在β-巯基乙醇(ME)存在下在 1.044、1.063 和 1.125kg/L 的背景密度下离心,用于分离脂蛋白亚组分和 Lp(a)。用 HPLC 分析超速离心底部级分中的胆固醇水平。

结果

ME 有效地将 Lp(a) 解离为载脂蛋白(a)和 Lp(a)残基[Lp(a)-]。Lp(a)-的密度分布与天然 Lp(a)不同。基于这些数据,开发了一种通过超速离心分离脂蛋白成亚组分和 Lp(a)的方法。分离的 HDL 和 LDL 亚组分未被 Lp(a)污染。该方法高度精确,测量 HDL2-C、HDL3-C、LDLa-C、LDLb-C 和 Lp(a)-C 的总 CV 分别为 0.85%-2.66%、0.87%-3.21%、0.86%-1.11%、2.59%-6.35%和 4.42%-12.29%。

结论

建立了一种通过超速离心和 HPLC 分离 HDL 和 LDL 亚组分以及 Lp(a)并同时测量胆固醇的新方法。它精确、灵敏,可用于研究或临床实验室的脂蛋白分析。

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