Interaction between hydroquinone and ascorbic acid derivatives: Quenching effect of organic solvents

Citation
K. Satoh et al., Interaction between hydroquinone and ascorbic acid derivatives: Quenching effect of organic solvents, ANTICANC R, 20(3A), 2000, pp. 1577-1581
Citations number
14
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
20
Issue
3A
Year of publication
2000
Pages
1577 - 1581
Database
ISI
SICI code
0250-7005(200005/06)20:3A<1577:IBHAAA>2.0.ZU;2-7
Abstract
The interaction between hydroquinone (HQ) and ascorbic acid analogs was inv estigated Semiquinone radicals (SQ .) generated by Ne were comparably scave nged by ascorbic acid, sodium ascorbate and ascorbate 6-palmitate, but much less efficiently by ascorbate 2,6-dipalmitate. Organic solvents, such as d imethysulfoxide (DMSO) or ethanol, which are utilized for solubilization of water-insoluble analogs, ascorbate 6-palmitate and ascorbate 2,6-dipalmita te, also scavenged SQ .. DMSO scavenged the SQ . more efficiently than etha nol. This suggests the importance of considering such a quenching. effect o f organic solvent in the study of the interaction between HQ and antioxidan ts. The involvement of the ascorbate radical for cytotoxicity induction is discussed.