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首页> 外文期刊>Analytica chimica acta >Enzymatic determination of cholesterol and triglycerides in serum lipoprotein profiles by asymmetrical flow field-flow fractionation with on-line, dual detection
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Enzymatic determination of cholesterol and triglycerides in serum lipoprotein profiles by asymmetrical flow field-flow fractionation with on-line, dual detection

机译:在线双重检测通过不对称流场-流分离酶法测定血清脂蛋白谱中的胆固醇和甘油三酸酯

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摘要

Alterations of lipoproteins (LPs) and related lipid levels in blood serum are correlated to the risk of coronary artery disease (CAD). Fast, possibly automated methods to obtain complete, multi-parametric LP profiles are therefore welcome to be developed for routine, clinical analysis practice. In this work, asymmetrical flow field-flow fractionation (AF4) with on-line, dual post-fractionation reaction detection (PFRD) is applied to develop a method for single-run, simultaneous quantification of cholesterol (CHOL) and triglycerides (TGs) in each fractionated LP class. The enzymatic reagents used for the post-fractionation reaction are available as commercial kits for certified, standard clinical protocols for the analysis of CHOL and TGs in serum. Using CHOL and glycerol as reference standards, a new procedure is applied to optimize the experimental conditions for PFRD-based, quantitative analysis. Upon optimized PFRD and AF4 conditions, results obtained for the determination of total CHOL (TC), TGs, HDL-cholesterol (HDL-C), and LDL-cholesterol (LDL-C) in a set of serum samples from healthy donors are found in agreement with the values provided by a clinical laboratory. The intra-day and inter-day precisions of the method were found always lower than 10% (CV). When the method was applied to serum samples from patients affected by sepsis, differences in CHOL and TG profiles between patients and healthy donors were observed.
机译:血清中脂蛋白(LPs)的变化和相关脂质水平与冠心病(CAD)的风险相关。因此,欢迎为常规的临床分析实践开发快速,可能自动的方法以获得完整的多参数LP曲线。在这项工作中,采用具有在线双重分级分离后反应检测(PFRD)的非对称流场流分级分离(AF4)来开发一种用于同时进行胆固醇(CHOL)和甘油三酸酯(TGs)定量的方法在每个细分的LP类中。分馏后反应所用的酶试剂可作为商业试剂盒获得,用于分析血清中CHOL和TG的认证标准临床方案。以CHOL和甘油为参考标准,采用了一种新程序来优化基于PFRD的定量分析的实验条件。在优化的PFRD和AF4条件下,发现了来自健康供体的一组血清样品中总CHOL(TC),TG,HDL-胆固醇(HDL-C)和LDL-胆固醇(LDL-C)的测定结果。符合临床实验室提供的值。发现该方法的日内和日间精度始终低于10%(CV)。当该方法应用于脓毒症患者的血清样本时,观察到患者与健康供体之间的CHOL和TG谱存在差异。

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