Togawa T, Ohsawa A, Kawanabe K, Tanabe S
Department of Analytical Chemistry, Meiji College of Pharmacy, Tokyo, Japan.
J Chromatogr B Biomed Sci Appl. 1997 Dec 19;704(1-2):83-8. doi: 10.1016/s0378-4347(97)00449-0.
Cysteine sulfinic acid (CSA) and hypotaurine (HT) were determined by electrochemical detection with a glassy carbon electrode at 0.95 V vs. Ag/AgCl. The separation of CSA and HT was accomplished by coupled-column liquid chromatography, consisting of an anion-exchange column and a cation-exchange column. For the determination of CSA and HT in rat tissues, a column-switching system was introduced to remove interferences from late-eluting endogenous substances. The limits of determination were 0.05 microM for both sulfinic acids. The average precisions (C.V.) over the concentration range of 0.05 to 5 microM were 4.3% for CSA and 4.2% for HT.