Ruiz J I, Ochoa B
Department of Physiology, University of the Basque Country Medical School, Bilbao, Spain.
J Lipid Res. 1997 Jul;38(7):1482-9.
A sensitive, rapid, and simple method is presented for the simultaneous quantitation of the major phospholipids and neutral lipids using an image analyzer after separation by one-dimensional thin-layer chromatography. A clear-cut separation of the lipids was achieved on one EDTA-impregnated chromatoplate with five step-wise developments. An image was acquired, and the integrated optical densities of the individual spots were quantitated by a camera-equipped image analyzer against an internal standard of cholesteryl formate. Calibration curves for each lipid followed linear or hyperbolic functions permitting quantification of as little as 0.015 nmol of lysophosphatidylcholine and as much as 7.50 nmol of triglyceride from a single application. Quantitation of the major lipids in human plasma by TLC and image analysis and standardized enzymatic methods were well correlated. The method is suitable for routine analysis of biological samples having lipid profiles as different as rat hepatocyte subcellular fractions, and very low density lipoproteins secreted by rat hepatocyte suspensions.
本文介绍了一种灵敏、快速且简单的方法,该方法通过一维薄层色谱分离后,使用图像分析仪同时定量主要磷脂和中性脂质。在一块经乙二胺四乙酸(EDTA)浸渍的色谱板上,通过五步连续展开实现了脂质的清晰分离。采集图像,配备相机的图像分析仪以甲酸胆固醇酯作为内标,对各个斑点的积分光密度进行定量。每种脂质的校准曲线遵循线性或双曲线函数,单次进样即可定量低至0.015 nmol的溶血磷脂酰胆碱和高达7.50 nmol的甘油三酯。通过薄层色谱法和图像分析对人血浆中主要脂质的定量结果与标准化酶法高度相关。该方法适用于对脂质谱差异很大的生物样品进行常规分析,如大鼠肝细胞亚细胞组分以及大鼠肝细胞悬液分泌的极低密度脂蛋白。