C-60 and water-soluble fullerene derivatives as antioxidants against radical-initiated lipid peroxidation

Citation
Ic. Wang et al., C-60 and water-soluble fullerene derivatives as antioxidants against radical-initiated lipid peroxidation, J MED CHEM, 42(22), 1999, pp. 4614-4620
Citations number
34
Categorie Soggetti
Chemistry & Analysis
Journal title
JOURNAL OF MEDICINAL CHEMISTRY
ISSN journal
00222623 → ACNP
Volume
42
Issue
22
Year of publication
1999
Pages
4614 - 4620
Database
ISI
SICI code
0022-2623(19991104)42:22<4614:CAWFDA>2.0.ZU;2-4
Abstract
C-60, vitamin E, and three C-60 derivatives (polar 1 and water-soluble C-3/ D(3)C(60)s) were examined for their antioxidant effects on prevention of li pid peroxidation induced by superoxide and hydroxyl radicals. The protectio n effect on lipid peroxidation was found to be in the sequence: C-60 greate r than or equal to vitamin E > 1 > none, for liposoluble antioxidants, and C3C60 much greater than D3C60 > none, for water-soluble ones. Fluorescence quenching of PyCH2COOH (Py = pyrene) by both C-3-. and D(3)C(60)s shows tha t the Stern-Volmer constant, K-SV, is about the same for both quenchers in aqueous solution. Upon addition of liposomes, the fluorescence quenching be comes more efficient: 5-fold higher in K-SV for C3C60 than for D3C60. When Py(CH2)(n)COOH (n = 1, 3, 5, 9, or 15) was incorporated in lipid membranes, the K(SV)s all were small and nearly equal for D3C60 but were quite large and different for C3C60 with the sequence: n = 1 < 3 < 5 < 9 < 15. The bett er protection effect of C3C60 on lipid peroxidation than that of D3C60 is a ttributed to its stranger interaction with membranes. Overall, the antioxid ation abilities of the compounds examined were rationalized in terms of the number of reactive sites, the location of antioxidant in lipid membranes, and the strength of interactions between antioxidants and membranes.