A rapid micro-scale procedure for determination of the total lipid profile.

LL Wu, GR Warnick, JT Wu, RR Williams… - Clinical …, 1989 - academic.oup.com
LL Wu, GR Warnick, JT Wu, RR Williams, JM Lalouel
Clinical chemistry, 1989academic.oup.com
We describe a one-day micro-scale procedure for determining the total lipid profile. Only
0.55 mL of plasma is needed for complete quantification of total cholesterol (TC), triglyceride
(TG), and all lipoproteins. After precipitation with dextran sulfate and magnesium, the high-
density lipoprotein (HDL) fraction was separated by centrifugation in an Eppendorf
microcentrifuge. Very-low-density lipoprotein (VLDL) was separated from low-density
lipoprotein (LDL) plus HDL in a Beckman TL 100 ultracentrifuge. TC, TG, and cholesterol in …
Abstract
We describe a one-day micro-scale procedure for determining the total lipid profile. Only 0.55 mL of plasma is needed for complete quantification of total cholesterol (TC), triglyceride (TG), and all lipoproteins. After precipitation with dextran sulfate and magnesium, the high-density lipoprotein (HDL) fraction was separated by centrifugation in an Eppendorf microcentrifuge. Very-low-density lipoprotein (VLDL) was separated from low-density lipoprotein (LDL) plus HDL in a Beckman TL 100 ultracentrifuge. TC, TG, and cholesterol in different lipoprotein fractions were measured enzymatically in a Baker "Encore II" automated analyzer. CVs, both within-day and day-to-day, were less than 3% for TG and TC, and less than 5% for HDL-C determinations. CVs for LDL-C and VLDL-C were less than 7.5% and 15%, respectively. Results by our micromethods (n = 66) agreed well with those by the conventional methods used at the Northwest Lipid Research Center, which are standardized against the Reference Methods of the Centers for Disease Control. Coefficients of correlation between the two methods were 0.98 for TC, 1.0 for TG, 0.98 for HDL-C, 0.94 for LDL-C, and 0.96 for VLDL-C. Results of electrophoresis on agarose gel and radioactivity-recovery studies indicate that our micro-centrifugation and slicing procedures result in clean separation of VLDL from other lipoproteins.
Oxford University Press