Abstract
Since retinoic acid (RA) and RA receptors are key developmental regulators during organogenesis, they might participate in the abnormal development of the prostate caused by early estrogen exposure. In order to test this assumption, a sensitive analytical method that can differentiate 9‐cis, 13‐cis, and all‐trans RA in small tissue samples (∼8 mg) is required. Since retinol is the metabolic precursor to RA, simultaneous quantification of retinol would also provide valuable information. Here, we report a liquid chromatography–mass spectrometry method for simultaneous determination of retinol and 9‐cis, 13‐cis, and all‐trans RA in rat prostate. Mass spectrometric signal responses for RA were compared using positive ion atmospheric‐pressure chemical ionization (APCI) and electrospray, as well as positive ion and negative ion APCI. Positive ion APCI was selected for all subsequent analysis for its better sensitivity, and to provide simultaneous determination of retinol and RA. Ventral prostate tissue samples were homogenized and extracted following simple protein precipitation without derivatization. Baseline separation of 9‐cis, 13‐cis, and all‐trans RA standards was obtained by using a non‐porous silica C~18~ column. Selected ion monitoring of the ions m/z 301 and m/z 269 was carried out for mass spectrometric quantitative analysis. The ion of m/z 301 corresponded to the protonated molecule of RA, whereas the ion of m/z 269 corresponded to loss of water or acetic acid from the protonated molecule of retinol or the internal standard retinyl acetate respectively. The method has a linear response over a concentration range of at least three orders of magnitude. The limit of quantitation was determined to be 702 fmol all‐trans RA injected on‐column. The method showed excellent intra‐ and inter‐assay reproducibility and good recovery, and is suitable for analyzing RA and retinol in small tissue samples (∼8 mg). Copyright © 2001 John Wiley & Sons, Ltd.