The scavenging of reactive oxygen species and the potential for cell protection by fullerenols with different isoelectric points

Fullerenols were known as the major water-soluble derivatives of fullerene that possess particular significance biological effects such as anticancer active and free radical scavengers. We have reported a novel method for purifying nanoparticles of fullerenols, which based on different isoelectric points (pIs). Consistent with their cytoprotective abilities, these samples can scavenge the stable 2,2diphenyl-1-picryhydrazyl (DPPH) radical in vitro with the following relative potencies: pI 7.0 > pI 5.29> pI 4.40> pI 2.81. The observed differences in free radical-scavenging capabilities support the hypothesis that physicochemical properties, such as surface chemistry induced differences in electron affinity, and degree of aggregation, influence the biological and biomedical activities of fullerenols with different pIs. These purified fullerenols with pI 2.81, pI 4.40, pI 5.29 and pI 7.0 were performed to determine the effect of purified fullerenols on cytotoxicity and DNA stability in Raw 264.7 cells. There no significantly different by statistical product and service solutions (SPSS) analysis. But only the sample of fullerenols with pI 2.81 caused obvious DNA damage to RAW264.7 cells in the continuous buffer system.

[1]  Shadi F Othman,et al.  Curcumin-loaded magnetic nanoparticles for breast cancer therapeutics and imaging applications , 2012, International journal of nanomedicine.

[2]  Juan Li,et al.  Separation and purification of fullerenols for improved biocompatibility , 2012 .

[3]  Markus Schulz,et al.  Genotoxicity investigations on nanomaterials: methods, preparation and characterization of test material, potential artifacts and limitations--many questions, some answers. , 2009, Mutation research.

[4]  Paul C. Wang,et al.  The scavenging of reactive oxygen species and the potential for cell protection by functionalized fullerene materials. , 2009, Biomaterials.

[5]  J. West,et al.  The Differential Cytotoxicity of Water-Soluble Fullerenes , 2004 .

[6]  Z. Chai,et al.  Influences of Structural Properties on Stability of Fullerenols. , 2004, The journal of physical chemistry. B.

[7]  E. Oberdörster Manufactured Nanomaterials (Fullerenes, C60) Induce Oxidative Stress in the Brain of Juvenile Largemouth Bass , 2004, Environmental health perspectives.

[8]  M. Prato,et al.  Fullerene derivatives: an attractive tool for biological applications. , 2003, European journal of medicinal chemistry.

[9]  K. O’Malley,et al.  Fullerene-based antioxidants and neurodegenerative disorders. , 2001, Parkinsonism & related disorders.

[10]  J. Wu,et al.  Polyhydroxylated C60, fullerenols, as glutamate receptor antagonists and neuroprotective agents , 2000, Journal of neuroscience research.

[11]  T. Tsuchiya,et al.  Effects of intracerebral microinjection of hydroxylated-[60]fullerene on brain monoamine concentrations and locomotor behavior in rats. , 2010, Journal of nanoscience and nanotechnology.

[12]  S. Doak,et al.  NanoGenotoxicology: the DNA damaging potential of engineered nanomaterials. , 2009, Biomaterials.

[13]  F. Lu,et al.  Free radical scavenging activity of water-soluble fullerenols , 1995 .