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采用半微高效液相色谱-电化学检测法测定氧化修饰低密度脂蛋白中的氧化甾醇。

Determination of oxysterols in oxidatively modified low-density lipoprotein by semi-micro high-performance liquid chromatography with electrochemical detection.

作者信息

Matsunaga Io, Hakamata Hideki, Sadohara Kazuhiro, Kakiuchi Kosuke, Kusu Fumiyo

机构信息

Department of Analytical Chemistry, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Horinouchi 1432-1, Hachioji, Tokyo, Japan.

出版信息

Anal Biochem. 2009 Oct 15;393(2):222-8. doi: 10.1016/j.ab.2009.06.032. Epub 2009 Jun 27.

Abstract

A simple method for the determination of oxysterols was developed by semi-micro high-performance liquid chromatography with electrochemical detection (semi-micro HPLC-ECD). Semi-micro HPLC-ECD was established using a C30 microbore column, acetonitrile containing 50 mmol/L LiClO(4) as a mobile phase, and an applied potential at +2.8V versus Ag/AgCl. The current peak height was linearly related to the amount of sterol injected from 12.5 to 250 pmol (r>0.999) with a relative standard deviation (RSD) of less than 2.9% (n=6). This method was applied to the determination of seven oxysterols in oxidatively modified low-density lipoprotein (Ox-LDL). Oxysterols were determined with a recovery of more than 78.0% and an RSD of less than 2.9% (n=6) except for 7-ketocholesterol. 7-Ketocholesterol was determined as a sum of intact 7-ketocholesterol and its degradation product on saponification, cholesta-3,5-dien-7-one, with a recovery of 98.0% and an RSD of 2.5% (n=6). From these results, the current method enabled the simultaneous determination of seven oxysterols without any derivatization, providing a useful tool for the assessment of oxysterol contents in Ox-LDL.

摘要

开发了一种通过半微高效液相色谱-电化学检测法(半微HPLC-ECD)测定氧化甾醇的简单方法。使用C30微径柱、含50 mmol/L LiClO(4)的乙腈作为流动相,并以相对于Ag/AgCl为+2.8V的施加电位建立了半微HPLC-ECD。电流峰高与12.5至250 pmol进样的甾醇量呈线性关系(r>0.999),相对标准偏差(RSD)小于2.9%(n=6)。该方法应用于氧化修饰低密度脂蛋白(Ox-LDL)中七种氧化甾醇的测定。除7-酮胆固醇外,氧化甾醇的回收率超过78.0%,RSD小于2.9%(n=6)。7-酮胆固醇被测定为完整的7-酮胆固醇及其皂化降解产物胆甾-3,5-二烯-7-酮的总和,回收率为98.0%,RSD为2.5%(n=6)。从这些结果来看,当前方法能够在无需任何衍生化的情况下同时测定七种氧化甾醇,为评估Ox-LDL中的氧化甾醇含量提供了一种有用的工具。

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