Inorganic nanoparticles enhance the production of reactive oxygen species (ROS) during the autoxidation of l-3,4-dihydroxyphenylalanine (l-dopa)

Chemosphere

Volumn 85, Issue 1, 2011, Pages 19-25

  Luna Velasco, Antonia ^a   Field, Jim A ^a   Cobo Curiel, Angel ^a   Sierra Alvarez, Reyes ^a  

^a University of Arizona   (United States)

Author keywords

Engineered nanomaterials; Metal oxides; Nanotoxicity; Oxygen radicals; Phenols

Indexed keywords

CERIUM OXIDE; ELECTRON SPIN RESONANCE SPECTROSCOPY; HEMATITE; MAMMALS; MANGANESE OXIDE; OXIDATION; OXYGEN; PARAMAGNETIC RESONANCE; PHENOLS; REDOX REACTIONS; SUSPENSIONS (FLUIDS);

ELECTRON PARAMAGNETIC RESONANCES (EPR); ENGINEERED NANOMATERIALS; INORGANIC NANOPARTICLE; L-3 ,4-DIHYDROXYPHENYLALANINE; METAL OXIDES; NANOTOXICITY; OXYGEN RADICAL; REACTIVE OXYGEN SPECIES;

NANOPARTICLES;

HYDROXYL RADICAL; IRON OXIDE; LEVODOPA; NANOPARTICLE; PHENOL DERIVATIVE; REACTIVE OXYGEN METABOLITE;

AQUEOUS SOLUTION; DYE; ELECTRON SPIN RESONANCE; HYDROXYL RADICAL; INORGANIC COMPOUND; MAMMAL; NANOTECHNOLOGY; PHENOLIC COMPOUND; REDOX CONDITIONS; TOXICITY;

ARTICLE; AUTOOXIDATION; CHEMICAL REACTION; ELECTRON SPIN RESONANCE; OXIDATION; OXIDATION REDUCTION REACTION;

MAMMALIA;

EID: 84860419249     PISSN: 00456535     EISSN: 18791298     Source Type: Journal    
DOI: 10.1016/j.chemosphere.2011.06.053     Document Type: Article

References (46)

1. Baun A., Hartmann N.B., Grieger K., Kusk K.O. Ecotoxicity of engineered nanoparticles to aquatic invertebrates: a brief review and recommendations for future toxicity testing. Ecotoxicology 2008, 17:387-395.
2. Borraccino R., Kharoune M., Giot R., Agathos S.N., Nyns E.J., Naveau H.P., Pauss A. Abiotic transformation of catechol and 1-naphthol in aqueous solution - influence of environmental factors. Water Res. 2001, 35:3729-3737.
3. Brunner T.J., Wick P., Manser P., Spohn P., Grass R.N., Limbach L.K., Bruinink A., Stark W.J. In vitro cytotoxicity of oxide nanoparticles: comparison to asbestos, silica, and the effect of particle solubility. Environ. Sci. Technol. 2006, 40:4374-4381.
4. Cathcart R., Schwiers E., Ames B.N. Detection of picomole levels of hydroperoxides using a fluorescent dichlorofluorescein assay. Anal. Biochem. 1983, 134:111-116.
5. Cervini-Silva J., Gilbert B., Fakra S., Friedrich S., Banfield J. Coupled redox transformations of catechol and cerium at the surface of a cerium(III) phosphate mineral. Geochim. Cosmochim. Acta 2008, 72:2454-2464.
6. Chen X.P., Zhong Z.F., Xu Z.T., Chen L.D., Wang Y.T. 2',7'-Dichlorodihydrofluorescein as a fluorescent probe for reactive oxygen species measurement: forty years of application and controversy. Free Radical Res. 2010, 44:587-604.
7. Choi O., Hu Z. Size dependent and reactive oxygen species related nanosilver toxicity to nitrifying bacteria. Environ. Sci. Technol. 2008, 42:4583-4588.
8. Di J.W., Bi S.P. UV-Vis spectroscopic study of aluminum-manganese cooperative effect on the melanin formation from DOPA oxidation. Spectrosc. Spect. Anal. 2005, 25:83-85.
9. Ema M., Kobayashi N., Naya M., Hanai S., Nakanishi J. Reproductive and developmental toxicity studies of manufactured nanomaterials. Reprod. Toxicol. 2010, 30:343-352.
10. Gomez-Toribio V., Garcia-Martin A.B., Martinez M.J., Martinez A.T., Guillen F. Enhancing the production of hydroxyl radicals by Pleurotus eryngii via quinone redox cycling for pollutant removal. Appl. Environ. Microbiol. 2009, 75:3954-3962.
11. Halliwell B., Whiteman M. Measuring reactive species and oxidative damage in vivo and in cell culture: how should you do it and what do the results mean?. Brit. J. Pharmacol. 2004, 142:231-255.
12. HaMai D., Bondy S.C. Oxidative basis of manganese neurotoxicity. Ann. NY Acad. Sci. 2004, 1012:129.
13. Heckert E.G., Seal S., Self W.T. Fenton-like reaction catalyzed by the rare earth inner transition metal cerium. Environ. Sci. Technol. 2008, 42:5014-5019.
14. 2 to bacteria Vibrio fischeri and crustaceans Daphnia magna and Thamnocephalus platyurus. Chemosphere 2008, 71:1308-1316.
15. Hosaka S., Obuki M., Nakajima J., Suzuki M. Comparative study of antioxidants as quenchers or scavengers of reactive oxygen species based on quenching of MCLA-dependent chemiluminescence. Luminescence 2005, 20:419-427.
16. Hu B.X., Chen C.H., Frueh S.J., Jin L., Joesten R., Suib S.L. Removal of aqueous phenol by adsorption and oxidation with doped hydrophobic cryptomelane-type manganese oxide (K-OMS-2) nanofibers. J. Pys. Chem. C 2010, 114:9835-9844.
17. Hussain S.M., Javorina A.K., Schrand A.M., Duhart H.M., Ali S.F., Schlager J.J. The interaction of manganese nanoparticles with PC-12 cells induces dopamine depletion. Toxicol. Sci. 2006, 92:456-463.
18. Izumi Y., Sawada H., Yamamoto N., Kume T., Katsuki H., Shimohama S., Akaike A. Iron accelerates the conversion of dopamine-oxidized intermediates into melanin and provides protection in SH-SY5Y cells. J. Neurosci. Res. 2005, 82:126-137.
19. Ju-Nam Y., Lead J.R. Manufactured nanoparticles: an overview of their chemistry, interactions and potential environmental implications. Sci. Total Environ. 2008, 400:396-414.
20. Keenan C.R., Goth-Goldstein R., Lucas D., Sedlak D.L. Oxidative stress induced by zero-valent iron nanoparticles and Fe(II) in human bronchial epithelial cells. Environ. Sci. Technol. 2009, 43:4555-4560.
21. 2 nanoparticles according to size fraction. Sci. Total Environ. 2010, 408:2268-2272.
22. Kovacic P., Somanathan R. Biomechanisms of nanoparticles (toxicants, antioxidants and therapeutics): electron transfer and reactive oxygen species. J. Nanosci. Nanotechnol. 2010, 10:7919-7930.
23. 2 nanowire-induced cytotoxicity in Hela cells. J. Nanosci. Nanotechnol. 2010, 10:397-404.
24. Limbach L.K., Wick P., Manser P., Grass R.N., Bruinink A., Stark W.J. Exposure of engineered nanoparticles to human lung epithelial cells: influence of chemical composition and catalytic activity on oxidative stress. Environ. Sci. Technol. 2007, 41:4158-4163.
25. Lin W.S., Huang Y.W., Zhou X.D., Ma Y.F. Toxicity of cerium oxide nanoparticles in human lung cancer cells. Int. J. Toxicol. 2006, 25:451-457.
26. Lipovsky A., Tzitrinovich Z., Friedmann H., Applerot G., Gedanken A., Lubart R. EPR study of visible light-induced ROS generation by nanoparticles of ZnO. J. Phys. Chem. C 2009, 113:15997-16001.
27. McBride M.B. Adsortion and oxidation of phenolic-compounds by iron and manganese oxides. Soil Sci. Soc. Am. J. 1987, 51:1466-1472.
28. Meng H., Xia T., George S., Nel A.E. A predictive toxicological paradigm for the safety assessment of nanomaterials. ACS Nano 2009, 3:1620-1627.
29. Misu Y., Kitahama K., Goshima Y. 3, 4-Dihydroxyphenylalanine as a neurotransmitter candidate in the central nervous system. Pharmacol. Ther. 2003, 97:117-137.
30. Munoz-Munoz J.L., Garcia-Molina F., Varon R., Tudela J., Garcia-Canovas F., Rodriguez-Lopez J.N. Generation of hydrogen peroxide in the melanin biosynthesis pathway. BBA Proteins Proteom. 2009, 1794:1017-1029.
31. Nel A., Xia T., Madler L., Li N. Toxic potential of materials at the nanolevel. Science 2006, 311:622-627.
32. Nowack B., Bucheli T.D. Occurrence, behavior and effects of nanoparticles in the environment. Environ. Pollut. 2007, 150:5-22.
33. Park E.J., Choi J., Park Y.K., Park K. Oxidative stress induced by cerium oxide nanoparticles in cultured BEAS-2B cells. Toxicology 2008, 245:90-100.
34. Phenrat T., Long T.C., Lowry G.V., Veronesi B. Partial oxidation (" aging" ) and surface modification decrease the toxicity of nanosized zerovalent iron. Environ. Sci. Technol. 2009, 43:195-200.
35. Rogers E.J., Hsieh S.F., Organti N., Schmidt D., Bello D. A high throughput in vitro analytical approach to screen for oxidative stress potential exerted by nanomaterials using a biologically relevant matrix: human blood serum. Toxicol. in Vitro 2008, 22:1639-1647.
36. Sauvain J.J., Deslarzes S., Riediker M. Nanoparticle reactivity toward dithiothreitol. Nanotoxicology 2008, 2:121-129.
37. Schrand A.M., Rahman M.F., Hussain S.M., Schlager J.J., Smith D.A., Syed A.F. Metal-based nanoparticles and their toxicity assessment. Wiley Interdisciplinary Rev. Nanomed. Nanobiotechnol. 2010, 2:544-568.
38. Serra P.A., Esposito G., Enrico P., Mura M.A., Migheli R., Delogu M.R., Miele M., Desole M.S., Grella G., Miele E. Manganese increases l-DOPA auto-oxidation in the striatum of the freely moving rat: potential implications to l-DOPA long-term therapy of Parkinson's disease. Brit. J. Pharmacol. 2000, 130:937-945.
39. Shin E.J., Miser D.E., Chan W.G., Hajaligol M.R. Catalytic cracking of catechols and hydroquinones in the presence of nano-particle iron oxide. Appl. Catal. B-Environ. 2005, 61:79-89.
40. Stefanescu D., Khoshnan A., Patterson P., Hering J. Neurotoxicity of manganese oxide nanomaterials. J. Nanopart. Res. 2009, 11:1957-1969.
41. Stone A.T. Reductive dissolution of manganese (III/IV) oxides by substituted phenols. Environ. Sci. Technol. 1987, 21:979-988.
42. Wilson M.R., Lightbody J.H., Donaldson K., Sales J., Stone V. Interactions between ultrafine particles and transition metals in vivo and in vitro. Toxicol. Appl. Pharmacol. 2002, 184:172-179.
43. Xia T., Kovochich M., Brant J., Hotze M., Sempf J., Oberley T., Sioutas C., Yeh J.I., Wiesner M.R., Nel A.E. Comparison of the abilities of ambient and manufactured nanoparticles to induce cellular toxicity according to an oxidative stress paradigm. Nano Lett. 2006, 6:1794-1807.
44. Zelmanov G., Semiat R. Phenol oxidation kinetics in water solution using iron(3)-oxide-based nano-catalysts. Water Res. 2008, 42:3848-3856.
45. Zhang H.C., Huang C.H. Oxidative transformation of triclosan and chlorophene by manganese oxides. Environ. Sci. Technol. 2003, 37:2421-2430.
46. 4 nanoparticles as catalysts for the catalytic oxidation of phenolic and aniline compounds. J. Hazard. Mater. 2009, 167:560-566.