Magnani H N, Howard A N
J Clin Pathol. 1971 Dec;24(9):837-45. doi: 10.1136/jcp.24.9.837.
A rapid, inexpensive, and quantitative method is described for obtaining the levels of plasma very low, low, and high density lipoproteins using cellulose acetate electrophoresis and lipid assays without prior separation by ultracentrifuge or other techniques. It involves separation of the lipoproteins by cellulose acetate electrophoresis, followed by their identification with the ozone-Schiff reaction. The total lipoprotein concentration is estimated from the total plasma phospholipid, and the percentage of each component obtained by densitometric analysis of the stained electrophoretograms, using reflected light. For samples with a raised level of very low density lipoprotein, plasma triglyceride analysis is also required. The results obtained by the cellulose acetate electrophoresis method are in good agreement with those by the analytical ultracentrifuge and the preparative ultracentrifuge with refractometry. The theoretical assumptions on which the method is based have been shown to be valid.
本文描述了一种快速、廉价且定量的方法,可用于在不预先通过超速离心或其他技术进行分离的情况下,利用醋酸纤维素电泳和脂质测定来获取血浆极低密度脂蛋白、低密度脂蛋白和高密度脂蛋白的水平。该方法包括通过醋酸纤维素电泳分离脂蛋白,随后用臭氧-席夫反应对其进行鉴定。根据血浆总磷脂估算总脂蛋白浓度,并通过对染色电泳图谱进行反射光密度分析获得各组分的百分比。对于极低密度脂蛋白水平升高的样本,还需要进行血浆甘油三酯分析。通过醋酸纤维素电泳法获得的结果与分析超速离心法和配备折射计的制备超速离心法的结果高度一致。已证明该方法所基于的理论假设是有效的。