Division of Metabolic Diseases and Nutritional Medicine, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University of Munich, Munich, Germany.
J Lipid Res. 2010 Jan;51(1):216-21. doi: 10.1194/jlr.D000547.
Plasma FA composition, a marker of FA status and dietary intake, is associated with health outcomes on a short- and long-term basis. Detailed investigation of the relationships between plasma FA composition and health requires the analysis of large numbers of samples, but manual sample preparation is very cumbersome and time consuming. We developed a high-throughput method for the analysis of FAs in plasma glycerophospholipids (GPs) with increased sensitivity. Sample preparation requires two simple steps: protein precipitation and subsequent base catalyzed methyl ester synthesis. Analysis of GP FAs is performed by gas chromatography. Coefficients of variation for FAs contributing more than 1% to total FAs are below 4%. Compared with the established reference method, results of the new method show good agreement and very good correlations (r > 0.9). The new method reduces the manual workload to about 10% of the reference method. Only 100 microl plasma volume is needed, which allows for the analysis of samples from infants. The method is well suitable for application in large clinical trials and epidemiological studies.
血浆 FA 组成是 FA 状态和饮食摄入的标志物,它与短期和长期的健康结果有关。详细研究血浆 FA 组成与健康之间的关系需要分析大量的样本,但手动样品制备非常繁琐和耗时。我们开发了一种高通量分析血浆甘油磷脂 (GP) 中 FA 的方法,该方法具有更高的灵敏度。样品制备只需两步简单的步骤:蛋白质沉淀和随后的碱催化甲酯合成。通过气相色谱法分析 GP FA。对占总 FA 超过 1%的 FA 的变异系数低于 4%。与已建立的参考方法相比,新方法的结果显示出良好的一致性和非常好的相关性(r > 0.9)。新方法将手动工作量减少到参考方法的约 10%。仅需 100 微升血浆体积,即可分析婴儿样本。该方法非常适合应用于大型临床试验和流行病学研究。