For the measurements of α-Tocopherol and Retinol, You have to deproteinized plasma with ethanol that contains the internal standards (α-tocopheryl acetate and retinyl acetate), and the lipid is extracted with hexane. After an aliquot of the solvent phase is evaporated, the residue is dissolved in diethyl ether and diluted with methanol. A portion of this solution is injected onto a C18 reversed-phase chromatographic column, and absorbance of the vitamins and internal standards are measured at 280 nm. Peak-height ratios are used to quantify each vitamin (Catignani and Bieri, 1983).