Beta-lipoprotein cholesterol quantitation with polycations.
- 1 March 1977
- journal article
- research article
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 23 (3) , 536-540
- https://doi.org/10.1093/clinchem/23.3.536
Abstract
We compared direct determination of beta-lipoprotein cholesterol after selective extraction of very-low-density and high-density lipoproteins from serum with poly(ethyleneimine) and a cation-exchange resin with the classical quantitation after lipoprotein fractionation with the ultracentrifuge. At beta-lipoprotein cholesterol concentrations between 1.50 and 5.00 g/liter the correlation is linear (r = 0.95). The precision for the extraction procedure is as good (CV 2.4-2.8%) as for the quantitation by ultracentrifugation (CV 3.2-6.0%). From solutions of isolated lipoproteins, very-low-density lipoproteins are 93% extracted and high-density lipoproteins 60%, but low-density-lipoproteins only 5%. The molecular mechanism of the extraction is supposed to be due to both hydrophobic interaction of long-chain fatty acid residues and ionic interaction of phospholipids located at the surface of very low-density and high-density lipoproteins and the lipophilic polycation.This publication has 3 references indexed in Scilit:
- Lipoprotein-elektrophorese in agarosegelClinica Chimica Acta; International Journal of Clinical Chemistry, 1968
- STUDIES OF METABOLISM OF RADIOIODINATED HUMAN SERUM ALPHA LIPOPROTEIN IN NORMAL + HYPERLIPIDEMIC SUBJECTS1964
- THE DISTRIBUTION AND CHEMICAL COMPOSITION OF ULTRACENTRIFUGALLY SEPARATED LIPOPROTEINS IN HUMAN SERUMJournal of Clinical Investigation, 1955