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Simultaneous Determination of High-Density Lipoprotein, Very Low-Density Lipoprotein and Low-Density Lipoprotein Subclass in Human Serum by Microchip CE

机译:Microchip CE同时测定人血清中高密度脂蛋白,极低密度脂蛋白和低密度脂蛋白亚类

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摘要

Lipoproteins, especially high-density lipoproteins (HDL), very low-density lipoproteins (VLDL) and small, dense low-density lipoprotein (sdLDL), are believed to play an important role in the development of atherosclerosis. In this work, a simple, selective and sensitive method for the simultaneous monitoring of these lipoproteins in human serum using microchip capillary electrophoresis was developed. Gold nanoparticles were used as an additive to the running buffer to obtain the absolute separation of the lipoproteins. Under optimised conditions, the linear ranges of large buoyant low-density lipoproteins, sdLDL, VLDL and HDL were 10–800, 10–800, 40–1,000 and 20–800 μg L−1, and their limits of detection were 5, 5, 15 and 8 μg L−1, respectively. The intraassay and interassay relative standard deviation of lipoprotein peak areas were in the range of 3.8–7.4%. For practical application, variations in the serum lipoprotein of coronary heart disease patients were monitored by microchip-based CE. The results showed that the method was applicable for routine clinical use and allowed the rapid detection of different lipoprotein classes as well as their subclasses, thus greatly improving the analysis of atherosclerotic risk factors.
机译:脂蛋白,特别是高密度脂蛋白(HDL),极低密度脂蛋白(VLDL)和小的,密集的低密度脂蛋白(sdLDL)被认为在动脉粥样硬化的发展中起重要作用。在这项工作中,开发了一种使用微芯片毛细管电泳同时监测人血清中这些脂蛋白的简单,选择性和灵敏的方法。金纳米颗粒用作运行缓冲液的添加剂,以实现脂蛋白的绝对分离。在优化条件下,大型浮力低密度脂蛋白,sdLDL,VLDL和HDL的线性范围分别为10–800、10–800、40–1,000和20–800μgL -1 检测限分别为5、5、15和8μgL -1 。脂蛋白峰面积的测定内和测定间相对标准偏差在3.8–7.4%的范围内。对于实际应用,可通过基于微芯片的CE监测冠心病患者血清脂蛋白的变化。结果表明,该方法适用于常规临床应用,可以快速检测出不同脂蛋白类别及其亚类,从而大大改善了动脉粥样硬化危险因素的分析。

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