Platinum nanoparticles inhibit antioxidant effects of vitamin C via ascorbate oxidase-mimetic activity12. Issue 48 (22nd November 2016)

• Record Type: Journal Article
• Authors: Chen, Chao; Fan, Sanhong; Li, Chen; Chong, Yu; Tian, Xin; Zheng, Jiwen; Fu, Peter P.; Jiang, Xiumei; Wamer, Wayne G.; Yin, Jun-jie
• Is Part Of: Journal of materials chemistry. Volume 4:Issue 48(2016)
• Page Start: 7895
• Page End: 7901
• Publication Date: 2016-11-22
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Biomedical materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c6tb02382g
• Languages: English
• ISSNs: 2050-750X

Abstract

Abstract : Pt nanoparticles with ascorbate oxidase-mimetic activity inhibit the cytoprotective effect of vitamin C on cells challenged by H2 O2 . Abstract : The development and application of nanomaterials as consumer products including food, drugs, and cosmetics are rapidly expanding. However, interactions between these novel materials and other chemical components of consumer products have not been thoroughly studied. Here, by using electron spin resonance techniques, we compared the effects of Au, Ag, and Pt nanoparticles (NPs) on the antioxidant activity of vitamin C (sodiuml -ascorbate, NaA). Chemical studies showed that Pt NPs exhibit ascorbate oxidase-mimetic activity, thereby oxidizing NaA but Au and Ag NPs do not. This ascorbate oxidase-mimetic activity of Pt NPs results in a dramatic loss of antioxidant activity of NaA for scavenging hydroxyl radicals and superoxide radicals. A further study suggested that the ascorbate oxidase-mimetic activity of Pt NPs is critically dependent on the particle size. Finally, in vitro cell studies demonstrated that Pt NPs with ascorbate oxidase-mimetic activity inhibit the cytoprotective effect of NaA on cells challenged by oxidative stress. Our findings provide a better understanding of enzyme-mimicking NP interactions with naturally-occurring antioxidants and should guide future applications.