M. Wronski, SEPARATION OF URINARY THIOLS AS TRIBUTYLTINMERCAPTIDES AND DETERMINATION USING CAPILLARY ISOTACHOPHORESIS, Journal of chromatography B. Biomedical applications, 676(1), 1996, pp. 29-34
Citations number
20
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
Journal title
Journal of chromatography B. Biomedical applications
The essential steps in the assay included electrolytic reduction of di
sulphides, neutralization, extraction of thiols with 0.1 M tributyltin
hydroxide in octane, stripping of the extract with 2% acetic acid, fi
xing the washed-out amino thiols to a cation exchanger, elution with 2
M hydrochloric acid, oxidation with bromine and evaporation. The rema
ining octane extract was decomposed by dodecanethiol, the mercapto aci
ds were washed out, oxidized with bromine and evaporated. Both residue
s were dissolved in water and analysed using capillary isotachophoresi
s at pH 3.0. Cysteamine was extracted from reduced urine at ca. pH 10,
decomposed by dodecanethiol and re-extracted to boric acid followed b
y determination as a cation. The presence of the following thiols in u
rine has been confirmed: mercaptoacetic acid, 3-mercaptolactic acid, 2
-mercaptopropionic acid, acetylcysteine, mercaptoethanol, cysteine, ho
mocysteine and an un-identified amino thiol. Cysteamine and 3-mercapto
propionic acid could not be detected. Captopril, homocysteine and cyst
eine were determined quantitatively.