Simultaneous determination of endogenous retinoic acid isomers and retinol in human plasma by isocratic normal-phase HPLC with ultraviolet detection

Abstract

We describe a rapid and simple procedure for the simultaneous quantitation of endogenous 13-cis-retinoic acid, all-trans-retinoic acid, and retinol by isocratic normal-phase HPLC with ultraviolet detection, in 0.5 mL of human plasma. A silica adsorption column was eluted with n-hexane:2-propanol:acetic acid (200:0.7:0.135 by vol) at 0.9 mL/min, and the effluent monitored at 350 nm. The arotinoid ethylsulfonic acid Ro 15-1570 was used as the internal standard. High sensitivity, allowing quantitation of physiological concentrations, was achieved, particularly for the retinoic acid isomers. The detection limits were 0.5 μg/L in plasma for both 13-cis- and trans-retinoic acid, and 10 μg/L for retinol. The CVs for between-day determinations of the lowest quality-control concentration (n = 12) were 4.8% for 13-cis-retinoic acid, 3.4% for transretinoic acid, and 3.0% for retinol. The mean (± SD) concentrations of 13-cis-retinoic acid (1.79 ± 0.56 μg/L), trans-retinoic acid (1.35 ± 0.42 μg/L), and retinol (533 ± 58 μg/L) measured in plasma from 22 healthy volunteers agreed well with those previously reported.