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Quantification of the lipid composition from TGRL and TGRL lipolysis treatments. Human postprandial TGRL was isolated by density gradient ultracentrifugation. Before the lipid assay, TGRL was incubated with LpL (2 U/ml) for 30 min at 37°C. Each lipid fraction was quantified by enzymatic assay. Data show the means ± SE of 3 independent analyses. *P < 0.01. FFA, free fatty acids; TG, triglyceride; PL, phospholipid.
