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A simple method to assess the oxidative susceptibility of low density lipoproteins

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Table 1: Recovery of 1.44 nmol MDA/tube added to duplicated re-suspended LDL samples obtained from three independent plas-ma samples.
Figure 1Kinetics of in vitro LDL peroxidation assessed byTBARS formation. An aliquot of 100 µl plasma from threedifferent patients (A, B, C) was assayed
Figure 2Basal and Cu2+ and H2O2 -induced LDL oxidation.Samples were incubated with EDTA (basal LDL oxidation),without additions, or in the presence of Cu2+ (100 µM) and/or H2O2 (300 ml/l)
Figure 4Agarose electrophoresis of whole plasma and LDLfractions. Bands correspond to: 1, LDL fraction obtained byselective precipitation; 2, whole plasma of a normolipidemicpatient; 3, whole plasma of a hyperlipidemic patient; 4, LDLfraction obtained by u

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