Determination of antioxidant capacity of thiol-containing compounds by electron spin resonance spectroscopy based on Cu 2+ ion reduction
Talanta, ISSN: 0039-9140, Vol: 184, Page: 23-28
2018
- 12Citations
- 19Captures
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Metrics Details
- Citations12
- Citation Indexes12
- 12
- CrossRef11
- Captures19
- Readers19
- 19
Article Description
Electron spin resonance spectroscopy was applied to determining the antioxidant capacity of eight thiol-containing compounds, including reduced glutathione, N-acetyl-L-cycsteine, methimazole, captopril, and tiopronin with one thiol group, 1,4-dithioerythritol and 2,3-dimercapto-1-propanol with two thiol groups, as well as L-cystine with no free thiol group. Cu 2+ ion gives an electron spin resonance signal and is reduced to Cu + ion with no electron spin resonance signal by the free thiol group in the compounds. Trolox equivalent antioxidant capacity (TEAC) was used to evaluate the reducing ability of the thiol-containing compounds and the TEAC values were found to be relevant to the number of thiol groups contained in the compounds. For the purpose of comparison, the UV-vis spectrophotometry, cupric reducing antioxidant capacity (CUPRAC) method, and Ellman assay were applied to the determination of the antioxidant capacity of the thiol-containing compounds. The TEAC values obtained by the present method were very close to those obtained by UV-vis method. However, compared with CUPRAC method, for methimazole the present method gave a more reasonable TEAC value. The present method was also applied to the quantification of N-acetyl-L-cycsteine, methimazole, captopril, and tiopronin in their pharmaceutical formulations.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0039914018302169; http://dx.doi.org/10.1016/j.talanta.2018.02.098; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85042685146&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/29674037; https://linkinghub.elsevier.com/retrieve/pii/S0039914018302169; https://dx.doi.org/10.1016/j.talanta.2018.02.098
Elsevier BV
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