Chromatographic characterization of proanthocyanidins after thiolysis withcysteamine

Citation
Jl. Torres et C. Lozano, Chromatographic characterization of proanthocyanidins after thiolysis withcysteamine, CHROMATOGR, 54(7-8), 2001, pp. 523-526
Citations number
16
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
CHROMATOGRAPHIA
ISSN journal
00095893 → ACNP
Volume
54
Issue
7-8
Year of publication
2001
Pages
523 - 526
Database
ISI
SICI code
0009-5893(200110)54:7-8<523:CCOPAT>2.0.ZU;2-N
Abstract
Cysteamine is proposed as a user-friendly thiol donor with application to t he analysis of proanthocyanidins by thiolysis. Oligomeric proanthocyanidins are potent antioxidants and disease-preventing agents. The efficiency of w hich depends on their composition and size. The degree of polymerization of proanthocyanidins is usually estimated by thiolysis then reversed-phase hi gh-performance liquid chromatography. The new derivatization procedure is a n alternative to the use of toluene-alpha -thiol as thiol donor. In additio n to enabling the direct chromatographic analysis of crude material, the am ino function introduced facilitates prior discrimination between terminal a nd extension flavanoid moieties by means of cation-exchange chromatography.