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开发一种质子核磁共振光谱法,用于通过单次快速测量来测定血浆脂蛋白浓度和亚类分布。

Development of a proton nuclear magnetic resonance spectroscopic method for determining plasma lipoprotein concentrations and subspecies distributions from a single, rapid measurement.

作者信息

Otvos J D, Jeyarajah E J, Bennett D W, Krauss R M

机构信息

Department of Biochemistry, North Carolina State University, Raleigh 27695.

出版信息

Clin Chem. 1992 Sep;38(9):1632-8.

PMID:1326420
Abstract

We are developing a method for quantifying plasma lipoproteins by proton nuclear magnetic resonance (NMR) spectroscopy that offers advantages over existing clinical methods. We showed that the major lipoproteins have distinct NMR properties sufficient to permit their concentrations to be extracted from a computer lineshape analysis of the plasma lipid methyl resonance envelope (Clin Chem 1991; 37:377-86). We have now discovered that the spectra of the subspecies within each lipoprotein class are different enough to influence the composite spectrum of that class and hence the spectrum of whole plasma. By including spectra representative of these subspecies as additional components in the lineshape-fitting analysis, a complete concentration profile of very-low-density, low-density (LDL), and high-density (HDL) lipoproteins plus the subspecies distributions within these classes can be simultaneously generated. A pilot study of 30 plasma samples of widely varied composition demonstrated good agreement between NMR-derived values and lipoprotein lipid concentrations and LDL and HDL subspecies distributions determined by gradient-gel electrophoresis.

摘要

我们正在开发一种通过质子核磁共振(NMR)光谱法定量血浆脂蛋白的方法,该方法比现有的临床方法具有优势。我们发现主要的脂蛋白具有独特的NMR特性,足以通过对血浆脂质甲基共振包络进行计算机线形分析来提取其浓度(《临床化学》1991年;37:377 - 86)。我们现在发现,每个脂蛋白类别内的亚类光谱差异足够大,足以影响该类别的复合光谱,进而影响全血浆的光谱。通过将代表这些亚类的光谱作为线形拟合分析中的附加成分,可同时生成极低密度、低密度(LDL)和高密度(HDL)脂蛋白的完整浓度分布图以及这些类别内的亚类分布。对30个成分差异很大的血浆样本进行的初步研究表明,NMR得出的值与脂蛋白脂质浓度以及通过梯度凝胶电泳测定的LDL和HDL亚类分布之间具有良好的一致性。

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