C60 and Water-Soluble Fullerene Derivatives as Antioxidants Against Radical-Initiated Lipid Peroxidation

C60, vitamin E, and three C60 derivatives (polar 1 and water-soluble C3/D3C60s) were examined for their antioxidant effects on prevention of lipid peroxidation induced by superoxide and hydroxyl radicals. The protection effect on lipid peroxidation was found to be in the sequence:  C60 ≥ vitamin E &...

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Veröffentlicht in:Journal of medicinal chemistry 1999-11, Vol.42 (22), p.4614-4620
Hauptverfasser: Wang, I Chen, Tai, Lin Ai, Lee, Don Dar, Kanakamma, P. P, Shen, Clifton K.-F, Luh, Tien-Yau, Cheng, Chien Hong, Hwang, Kuo Chu
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container_end_page 4620
container_issue 22
container_start_page 4614
container_title Journal of medicinal chemistry
container_volume 42
creator Wang, I Chen
Tai, Lin Ai
Lee, Don Dar
Kanakamma, P. P
Shen, Clifton K.-F
Luh, Tien-Yau
Cheng, Chien Hong
Hwang, Kuo Chu
description C60, vitamin E, and three C60 derivatives (polar 1 and water-soluble C3/D3C60s) were examined for their antioxidant effects on prevention of lipid peroxidation induced by superoxide and hydroxyl radicals. The protection effect on lipid peroxidation was found to be in the sequence:  C60 ≥ vitamin E > 1 > none, for liposoluble antioxidants, and C3C60 ≫ D3C60 > none, for water-soluble ones. Fluorescence quenching of PyCH2COOH (Py = pyrene) by both C3- and D3C60s shows that the Stern−Volmer constant, K SV, is about the same for both quenchers in aqueous solution. Upon addition of liposomes, the fluorescence quenching becomes 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 SVs 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 better protection effect of C3C60 on lipid peroxidation than that of D3C60 is attributed to its stronger interaction with membranes. Overall, the antioxidation 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.
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P ; Shen, Clifton K.-F ; Luh, Tien-Yau ; Cheng, Chien Hong ; Hwang, Kuo Chu</creator><creatorcontrib>Wang, I Chen ; Tai, Lin Ai ; Lee, Don Dar ; Kanakamma, P. P ; Shen, Clifton K.-F ; Luh, Tien-Yau ; Cheng, Chien Hong ; Hwang, Kuo Chu</creatorcontrib><description>C60, vitamin E, and three C60 derivatives (polar 1 and water-soluble C3/D3C60s) were examined for their antioxidant effects on prevention of lipid peroxidation induced by superoxide and hydroxyl radicals. The protection effect on lipid peroxidation was found to be in the sequence:  C60 ≥ vitamin E &gt; 1 &gt; none, for liposoluble antioxidants, and C3C60 ≫ D3C60 &gt; none, for water-soluble ones. Fluorescence quenching of PyCH2COOH (Py = pyrene) by both C3- and D3C60s shows that the Stern−Volmer constant, K SV, is about the same for both quenchers in aqueous solution. Upon addition of liposomes, the fluorescence quenching becomes more efficient:  5-fold higher in K SV for C3C60 than for D3C60. 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Upon addition of liposomes, the fluorescence quenching becomes 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 SVs all were small and nearly equal for D3C60 but were quite large and different for C3C60 with the sequence:  n = 1 &lt; 3 &lt; 5 &lt; 9 &lt; 15. The better protection effect of C3C60 on lipid peroxidation than that of D3C60 is attributed to its stronger interaction with membranes. Overall, the antioxidation 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.</description><subject>Biological and medical sciences</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Medical sciences</subject><subject>Pharmacology. 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Fluorescence quenching of PyCH2COOH (Py = pyrene) by both C3- and D3C60s shows that the Stern−Volmer constant, K SV, is about the same for both quenchers in aqueous solution. Upon addition of liposomes, the fluorescence quenching becomes 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 SVs all were small and nearly equal for D3C60 but were quite large and different for C3C60 with the sequence:  n = 1 &lt; 3 &lt; 5 &lt; 9 &lt; 15. The better protection effect of C3C60 on lipid peroxidation than that of D3C60 is attributed to its stronger interaction with membranes. 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subjects Biological and medical sciences
General and cellular metabolism. Vitamins
Medical sciences
Pharmacology. Drug treatments
title C60 and Water-Soluble Fullerene Derivatives as Antioxidants Against Radical-Initiated Lipid Peroxidation
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