Photodynamic activity of platinum(IV) chloride surface-modified TiO2 irradiated with visible light

Free Radical Biology and Medicine

Volumn 44, Issue 6, 2008, Pages 1120-1130

  Jańczyk, Agnieszka ^a   Wolnicka Głubisz, Agnieszka ^a   Urbanska, Krystyna ^a   Kisch, Horst ^b   Stochel, Grazyna ^a   Macyk, Wojciech ^a  

^a JAGIELLONIAN UNIVERSITY   (Poland)

^b UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

Mouse melanoma; Photocatalysis; Photodynamic therapy; Phototoxicity; Reactive oxygen species; Titanium dioxide

Indexed keywords

PLATINUM; REACTIVE OXYGEN METABOLITE; SODIUM AZIDE; TITANIUM DIOXIDE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; ARTICLE; CELL MEMBRANE; CELL VIABILITY; CONTROLLED STUDY; DNA ADDUCT; MELANOMA CELL; MOUSE; NONHUMAN; OXYGEN CONSUMPTION; PEROXIDATION; PHOTOCATALYSIS; PHOTODYNAMICS; PHOTOSENSITIZATION; PHOTOTOXICITY; PRIORITY JOURNAL;

ANIMALS; CELL LINE, TUMOR; LIGHT; MICE; NECROSIS; PHOTOCHEMOTHERAPY; PHOTOSENSITIZING AGENTS; PLATINUM COMPOUNDS; REACTIVE OXYGEN SPECIES; SPIN TRAPPING; TITANIUM;

EID: 39949084687     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2007.12.019     Document Type: Article

References (65)

1. Szacilowski K., Macyk W., Drzewiecka-Matuszek A., Brindell M., and Stochel G. Bioinorganic photochemistry: frontiers and mechanism. Chem. Rev. 105 (2005) 2647-2694
2. Bonnett R. Chemical Aspects of Photodynamic Therapy (2000), Gordon and Breach, Amsterdam
3. 2 Photocatalysis: fundamentals and applications (1999), BKC Inc., Tokyo
4. Hoffmann M.R., Martin S.T., Choi W., and Bahnemann D.W. Environmental applications of semiconductor photocatalysis. Chem. Rev. 95 (1995) 69-96
5. 2 surfaces: principles, mechanisms, and selected results. Chem. Rev. 95 (1995) 735-758
6. Fujishima A., Rao T.N., and Tryk D.A. Titanium dioxide photocatalysis. J. Photochem. Photobiol., C Photochem. Rev. 1 (2000) 1-21
7. Konaka R., Kasahara E., Dunlap W.C., Yamamoto Y., Chien K.C., and Inoue M. Irradiation of titanium dioxide generates both singlet oxygen and superoxide anion. Free Radic. Biol. Med. 27 (1999) 294-300
8. 2 photocatalyst. J. Photochem. Photobiol., A Chem. 134 (2000) 139-142
9. Macyk W., Franke A., and Stochel G. Metal compounds and small molecules activation - case studies. Coord. Chem. Rev. 249 (2005) 2437-2457
10. Kisch H., and Macyk W. Visible-light photocatalysis by modified titania. ChemPhysChem 3 (2002) 399-400
11. Nakagawa Y., Wakuri S., Sakamoto K., and Tanaka N. The photogenotoxity of titanium dioxide particles. Mutat. Res. 394 (1997) 125-132
12. 2-UVA treatment. Toxicol. In Vitro 16 (2002) 629-635
13. 2 particles on U937 cells. J. Photochem. Photobiol., A Chem. 108 (1997) 229-233
14. Wamer W.G., Yin J.-J., and Wei R.R. Oxidative damage to nucleic acids photosensitizer by titanium dioxide. Free Radic. Biol. Med. 23 (1997) 851-858
15. Lu P.-J., Ho I.-C., and Lee T.-C. Induction of sister chromatid exchanges and micronuclei by titanium dioxide in Chinese hamster ovary-K1 cells. Mutat. Res. 414 (1998) 15-20
16. 2 nanoparticles through OH-radicals induced malignant cells to necrosis. Supramol. Sci. 5 (1998) 449-451
17. Mills A., and Le Hunte S. An overview of semiconductor photocatalysis. J. Photochem. Photobiol., A Chem. 108 (1997) 1-35
18. Blake D.M., Maness P.-C., Huang Z., Wolfrum E.J., Huang J., and Jacoby W.A. Application of the photocatalytic chemistry of titanium dioxide to disinfection and the killing of cancer cells. Sep. Purif. Methods 28 (1999) 1-50
19. DeRosa M.C., and Crutchley J. Photosensitized singlet oxygen and its applications. Coord. Chem. Rev. 233-234 (2002) 351-371
20. 2 particles on UV induced pyrimidine dimer formation. J. Photochem. Photobiol., A Chem. 141 (2001) 225-230
21. Hirakawa K., Mori M., Yoshida M., Oikawa S., and Kawanishi S. Photo-irradiated titanium dioxide catalyzes site specific DNA damage via generation of hydrogen peroxide. Free Radic. Res. 38 (2004) 439-447
22. 2 ultrafine particles. Biochim. Biophys. Acta 1200 (1994) 259-265
23. Matsunaga T., Tomoda T., Nakajima T., and Wake H. Photochemical sterilization of microbial cells by semiconductor powder. FEMS Microbiol. Lett. 29 (1985) 211-214
24. 2 thin film: dynamic view of the active oxygen species responsible for the effect. J. Photochem. Photobiol., A Chem. 106 (1997) 51-56
25. 2 thin film. J. Photochem. Photobiol., A Chem. 156 (2003) 227-233
26. Huang Z., Maness P.-C., Blade D.M., Wolfram E.J., Smolinski A.L., and Jacoby W.J. Bactericidal mode of titanium dioxide photocatalysis. J. Photochem. Photobiol., A Chem. 130 (2000) 163-170
27. Mitoraj D., Jańczyk A., Strus M., Kisch H., Stochel G., Heczko P.B., and Macyk W. Visible light inactivation of bacteria and fungi by modified titanium dioxide. Photochem. Photobiol. Sci. 6 (2007) 642-648
28. Yu J.C., Xie Y., Tang H.Y., Zhang L., Chan H.C., and Zhao J. Visible light-assisted bactericidal effect of metalphalocyanine-sensitized titanium dioxide films. J. Photochem. Photobiol., A Chem. 156 (2003) 235-241
29. Shieh K.-J., Li M., Lee Y.-H., Sheu S.-D., Liu Y.-T., and Wang Y.-C. Antibacterial performance of photocatalyst thin film fabricated by defection effect in visible light. Nanomed. Nanotechnol. Biol. Med. 2 (2006) 121-126
30. Kisch H., Burgeth G., and Macyk W. Visible light photocatalysis by a titania transition metal complex. Adv. Inorg. Chem. 56 (2004) 241-259
31. Macyk W., and Kisch H. Photosensitization of crystalline and amorphous titanium dioxide by platinum(IV) chloride surface complexes. Chem. Eur. J. 7 (2001) 1862-1867
32. 2. Photochem. Photobiol. Sci. 2 (2003) 322-328
33. Barr D. A step-by-step procedure for spin-trapping the hydroxyl radical. EPR experimental techniques (2003). http://www.bruker-biospin.com www.bruker-biospin.com
34. Burgeth G., and Kisch H. Photocatalytic and photoelectrochemical properties of titania-chloroplatinate(IV). Coord. Chem. Rev. 230 (2002) 40-47
35. Chakraborty A.K., Funasaka Y., Slominski A., Ermak G., Hwang J., Pawelek J.M., and Ichihaski M. Production and release of proopiomelanocortin (POMC) derived peptides by human melanocytes and keratinocytes in culture: regulation by ultraviolet B. Biochem. Biophys. Acta 1313 (1996) 130-138
36. Jańczyk A., Wolnicka-Głubisz A., Chmura A., Elas M., Matuszak Z., Stochel G., and Urbańska K. NO-dependent phototoxicity of Roussin's black salt against cancer cells. Nitric Oxide: Biol. Chem. 10 (2004) 42-50
37. Apoptosis, cell death and cell proliferation. https://www.roche-applied-science.com/PROD_INF/MANUALS/CELL_MAN/cell_toc.html. Roche Applied Science, Roche Diagnostics Corporation (2005)
38. Denizot F., and Lang R. Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability. J. Immunol. Methods 89 (1986) 271-277
39. Allen S., Sotos J., Sylte M.J., and Czuprynski C.J. Use of Hoechst 33342 staining to detect apoptotic changes in bovine mononuclear phagocytes infected with Mycobacterium avium sbsp. paratuberculosis. Clin. Diagn. Lab. Immunol. (2001) 460-464
40. ATP Determination Kit (A-22066). Molecular probes, product information (2003)
41. Spałek T., Pietrzyk P., and Sojka Z. Program EPRsim32. J. Chem. Inf. Model. 45 (2005) 18-29
42. Buettner G.R. Spin trapping: ESR parameters of spin adducts. Free Radic. Biol. Med. 3 (1987) 259-303
43. 2) radical in aqueous solutions: first ESR evidence of formation of new nitroxide radicals. Free Radic. Med. 20 (1996) 837-841
44. Hyde J.S., and Subczyński W.K. Spin-label oximetry (1989), Plenum, New York
45. Halpern H.J., Peric M., Nguyen T.D., Spencer D.P., Teichner B.A., Lin Y.J., and Bowman M.K. Selective isotopic labeling of a nitroxide spin label to enhance sensitivity for T2 oxymetry. J. Magn. Reson. 90 (1990) 40-51
46. Desoize B., and Madoulet C. Particular aspects of platinum compounds used at present in cancer treatment. Crit. Rev. Oncol./Hematol. 42 (2002) 317-325
47. Hall M.D., and Hambley T.W. Platinum(IV) antitumour compounds: their bioinorganic chemistry. Coord. Chem. Rev. 232 (2002) 49-67
48. Gebel T., Lantzsch H., Plessow K., and Dunkelberg H. Genotoxicity of platinum and palladium compounds in human and bacterial cells. Mutat. Res. 389 (1997) 183-190
49. Lebwohl D., and Canetta R. Clinical development of platinum complexes in cancer therapy: an historical perspective and an update. Eur. J. Cancer 34 (1998) 1522-1534
50. Kiesslich T., Oberdanner C.B., Krammer B., and Plaetzer K. Fast and reliable determination of intracellular ATP from cells cultured in 96-well microplates. J. Biochem. Biophys. Methods 57 (2003) 247-251
51. Leist M., Single B., Castoldi A.F., Kuhnle S., and Nicotera P. Intracellular adenosine triphosphate (ATP) concentration: a switch in the decision between apoptosis and necrosis. J. Exp. Med. 185 (1997) 1481-1486
52. Halliwell B., and Gutteridge J.M.C. Free Radicals in Biology and Medicine (1999), Oxford University Press, Oxford
53. Monroe B.M. Singlet oxygen in solution: lifetime and reaction rate constants (1985), CRC Press, Boca Raton, FL
54. Dorfman L.M., and Adams G.E. Reactivity of the hydroxyl radical in aqueous solutions (1973), National Bureau of Standards, Washington No. C13
55. Jańczyk A., Krakowska E., Stochel G., and Macyk W. Singlet oxygen photogeneration at surface modified titanium dioxide. J. Am. Chem. Soc. 128 (2006) 15574-15575
56. Finkelstein E., Rosen G.M., and Rauckamnn E.J. Spin trapping of superoxide and hydroxyl radical: practical aspects. Arch. Biochem. Biophys. 200 (1980) 1-16
57. 2-reactive species in oxygen toxicity in biology. J. Biol. Chem. 265 (1990) 13589-13594
58. Leonard S., Gannett P.M., Rojanasakul Y., Schwegler-Berry D., Castranova V., Vallyathan V., and Shi X. Cobalt-mediated generation of reactive oxygen species and its possible mechanism. J. Inorg. Biochem. 70 (1998) 239-244
59. Ohnishi S., Murata M., and Kawanishi S. DNA damage induced by hypochlorite and hypobromite with reference to inflammation-associated carcimogenesis. Cancer Lett. 178 (2002) 37-42
60. Ben-Hur E., Carmichael A., Riesz P., and Rosenthal I. Photochemical generation of superoxide radical and the cytotoxicity of phthalocyanines. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 48 (1985) 837-846
61. Sakthivel S., and Kisch H. Daylight photocatalysis by carbon-modified titanium dioxide. Angew. Chem., Int. Ed. Engl. 42 (2003) 4908-4911
62. Ollis D.F., Pelizzetti E., and Serpone N. Destruction of water contaminats. Environ. Sci. Technol. 25 (1991) 1523-1529
63. Zavodnik I.B., Lapshina E.A., Zavodnik L.B., Łabieniec M., Bryszewska M., and Reiter R.J. Hypochlorous acid-induced oxidative stress in Chinese hamcster B14 cells: viability, DNA and protein damage and the protective action of melatonin. Genet. Toxicol. Environ. Mutagen. 559 (2004) 39-48
64. Winterbourn C.C. Biological reactivity and biomarkers of neutrophil oxidants, hypochlorous acid. Toxicology 181-182 (2002) 223-227
65. Marcinkiewicz J., Chain B., Nowak B., Grabowska A., Bryniarski K., and Baran J. Antimicrobial and cytotoxic activity of hypochlorous acid interactions with taurine and nitrite. Inflamm. Res. 49 (2000)