Generation of nitrogen oxide and oxygen radicals by quantum dots

Journal of Biomedical Nanotechnology

Volumn 4, Issue 4, 2008, Pages 450-456

  Juzenas, Petras ^a   Generalov, Roman ^a   Juzeniene, Asta ^a   Moan, Johan ^a,b  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF OSLO   (Norway)

Author keywords

Lysosomal breakage; Nanosensitizer; Oxidation; Peroxynitrite; Photochemical internalization (PCI); Photodynamic therapy (PDT); Photosensitization; Radical assay; Reactive oxygen and nitrogen species (RONS); Singlet oxygen

Indexed keywords

CADMIUM COMPOUNDS; COMPUTER PERIPHERAL EQUIPMENT; FLUORESCENCE; HEAVY METALS; INTERFACES (COMPUTER); NITRIC OXIDE; NITROGEN; NITROGEN OXIDES; NONMETALS; OPTICAL MATERIALS; OPTICAL WAVEGUIDES; OXIDATION; OXIDES; OXYGEN; PHOTODYNAMIC THERAPY; PHOTOOXIDATION; PHOTOSENSITIZERS; PLASMONS; QUANTUM ELECTRONICS; ZINC SULFIDE;

LYSOSOMAL BREAKAGE; NANOSENSITIZER; PEROXYNITRITE; PHOTOCHEMICAL INTERNALIZATION (PCI); PHOTOSENSITIZATION; RADICAL ASSAY; REACTIVE OXYGEN AND NITROGEN SPECIES (RONS); SINGLET OXYGEN;

SEMICONDUCTOR QUANTUM DOTS;

ANION; ANTHRACENE DERIVATIVE; DIHYDRORHODAMINE 123; NITRIC OXIDE; NITROGEN OXIDE; OXYGEN RADICAL; PEROXYNITRITE; QUANTUM DOT; SINGLET OXYGEN; SUPEROXIDE;

ANIMAL EXPERIMENT; ANIMAL TISSUE; AQUEOUS SOLUTION; ARTICLE; BLUE LIGHT; CANCER CELL; CONTROLLED STUDY; FLUORESCENCE; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; IN VITRO STUDY; INTERNALIZATION; LYSOSOME; MALE; MOUSE; NONHUMAN; PHOTOACTIVATION; PHOTODYNAMIC THERAPY; PHOTOOXIDATION; PROSTATE CARCINOMA; RED LIGHT; SKIN;

EID: 58149316190     PISSN: 15507033     EISSN: 15507041     Source Type: Journal    
DOI: 10.1166/jbn.2008.008     Document Type: Article

References (71)

1. M. Ferrari, Cancer nanotechnology: Opportunities and challenges. Nat. Rev. Cancer 5, 161 (2005).
2. J. K. Jaiswal, H. Mattoussi, J. M. Mauro, and S. M. Simon, Longterm multiple color imaging of live cells using quantum dot bioconjugates. Nat. Biotechnol. 21, 47 (2003).
3. X. Wu, H. Liu, J. Liu, K. N. Haley, J. A. Treadway, J. P. Larson, N. Ge, F. Peale, and M. P. Bruchez, Immunofluorescent labeling of cancer marker Her2 and other cellular targets with semiconductor quantum dots. Nat. Biotechnol. 21, 41 (2003).
4. T. M. Jovin, Quantum dots finally come of age. Nat. Biotechnol. 21, 32 (2003).
5. A. M. Smith, X. Gao, and S. Nie, Quantum dot nanocrystals for in vivo molecular and cellular imaging. Photochem. Photobiol. 80, 377 (2004).
6. W. Jiang, E. Papa, H. Fischer, S. Mardyani, and W. C. Chan, Semi-conductor quantum dots as contrast agents for whole animal imaging. Trends Biotechnol. 22, 607 (2004).
7. J. Moan and Q. Peng, An outline of the hundred-year history of PDT. Anticancer Res. 23, 3591 (2003).
8. T. J. Dougherty, C. J. Gomer, B. W. Henderson, G. Jori, D. Kessel, M. Korbelik, J. Moan, and Q. Peng, Photodynamic therapy. J. Natl. Cancer Inst. 90, 889 (1998).
9. D. E. Dolmans, D. Fukumura, and R. K. Jain, Photodynamic therapy for cancer. Nat. Rev. Cancer 3, 380 (2003).
10. J. Fuchs and J. Thiele, The role of oxygen in cutaneous photodynamic therapy. Free Radic. Biol. Med. 24, 835 (1998).
11. M. Niedre, M. S. Patterson, and B. C. Wilson, Direct near-infrared luminescence detection of singlet oxygen generated by photodynamic therapy in cells in vitro and tissues in vivo. Photochem. Photobiol. 75, 382 (2002).
12. A. W. Girotti, Photosensitized oxidation of membrane lipids: Reaction pathways, cytotoxic effects, and cytoprotective mechanisms. J. Photochem. Photobiol. B 63, 103 (2001).
13. P. Juzenas and J. Moan, Singlet oxygen in photosensitization. J. Environ. Pathol. Toxicol. Oncol. 25, 29 (2006).
14. M. Kasha and D. E. Brabham, Singlet oxygen electronic structure and photosensitization. Singlet Oxygen, edited by H. H. Wasserman and R. W. Murray, Academic Press, New York, San Francisco, London (1979), pp. 1-33.
15. D. Weldon, T. D. Poulsen, K. V. Mikkelsen, and P. R. Ogilby, Singlet sigma: The "Other" singlet oxygen in solution. Photochem. Photobiol. 70, 369 (1999).
16. M. C. DeRosa and R. J. Crutchley, Photosensitized singlet oxygen and its applications. Coord. Chem. Rev. 233-234, 351 (2002).
17. R. Schmidt, Photosensitized generation of singlet oxygen. Photochem. Photobiol. 82, 1161 (2006).
18. J. Moan, On the diffusion length of singlet oxygen in cells and tissues. J. Photochem. Photobiol. B 6, 343 (1990).
19. I. E. Kochevar, Singlet oxygen signaling: From intimate to global. Sci. STKE 2004, e7 (2004).
20. W. Chen, Nanoparticle fluorescence based technology for biological applications. J. Nanosci. Nanotechnol. 8, 1019 (2008).
21. R. Bakalova, H. Ohba, Z. Zhelev, M. Ishikawa, and Y. Baba, Quantum dots as photosensitizers? Nat. Biotechnol. 22, 1360 (2004).
22. M. E. Akerman, W. C. Chan, P. Laakkonen, S. N. Bhatia, and E. Ruoslahti, Nanocrystal targeting in vivo. Proc. Natl. Acad. Sci. USA 99, 12617 (2002).
23. J. R. Lakowicz, Introduction to fluorescence. Principles of Fluorescence Spectroscopy, Springer Science + Business Media, LLC, New York (2006), pp. 1-26.
24. A. Juzeniene, K. P. Nielsen, and J. Moan, Biophysical aspects of photodynamic therapy. J. Environ. Pathol. Toxicol. Oncol.25, 7 (2006).
25. M. G. Bawendi, P. J. Carroll, W. L. Wilson, and L. E. Brus, Luminescence properties of CdSe quantum crystallites: Resonance between interior and surface localized states. J. Chem. Phys. 96, 946 (1992).
26. A. C. Samia, S. Dayal, and C. Burda, Quantum dot-based energy transfer: Perspectives and potential for applications in photodynamic therapy. Photochem. Photobiol. 82, 617 (2006).
27. C. Schweitzer and R. Schmidt, Physical mechanisms of generation and deactivation of singlet oxygen. Chem. Rev. 103, 1685 (2003).
28. A. A. Krasnovsky, Jr., Primary mechanisms of photoactivation of molecular oxygen. History of development and the modern status of research. Biochemistry (Mosc) 72, 1065 (2007).
29. Z.-Q. You, C.-P. Hsu, and G. R. Fleming, Triplet-triplet energy-transfer: Theory and calculation. J. Chem. Phys. 124, 1 (2006).
30. A. C. Samia, X. Chen, and C. Burda, Semiconductor quantum dots for photodynamic therapy. J. Am. Chem. Soc. 125, 15736 (2003).
31. Q. Chen, Q. Ma, Y. Wan, X. Su, Z. Lin, and Q. Jin, Studies on fluorescence resonance energy transfer between dyes and water-soluble quantum dots. Luminescence 20, 251 (2005).
32. Y. Liu, Y. Zhang, S. Wang, C. Pope, and W. Chen, Optical behaviors of ZnO-porphyrin conjugates and their potential applications for cancer treatment. Appl. Phys. Lett. 92, 143901 (2008).
33. Y. Liu, W. Chen, Y. Wang, and A. G. Joly, Investigation of water-soluble X-ray luminescence nanoparticles for photodynamic activation. Appl. Phys. Lett. 92, 043901 (2008).
34. W. Chen and J. Zhang, Using nanoparticles to enable simultaneous radiation and photodynamic therapies for cancer treatment. J. Nanosci. Nanotechnol. 6, 1159 (2006).
35. L. Shi, B. Hernandez, and M. Selke, Singlet oxygen generation from water-soluble quantum dot-organic dye nanocomposites. J. Am. Chem. Soc. 128, 6278 (2006).
36. J. M. Tsay, M. Trzoss, L. Shi, X. Kong, M. Selke, M. E. Jung, and S. Weiss, Singlet oxygen production by peptide-coated quantum dot-photosensitizer conjugates. J. Am. Chem. Soc. 129, 6865 (2007).
37. Y. Zhang, K. Aslan, M. J. Previte, and C. D. Geddes, Plasmonic engineering of singlet oxygen generation. Proc. Natl. Acad. Sci. USA 105, 1798 (2008).
38. P. Wardman, Fluorescent and luminescent probes for measurement of oxidative and nitrosative species in cells and tissues: Progress, pitfalls, and prospects. Free Radic. Biol. Med. 43, 995 (2007).
39. J. P. Crow, Dichlorodihydrofluorescein and dihydrorhodamine 123 are sensitive indicators of peroxynitrite in vitro: Implications for intracellular measurement of reactive nitrogen and oxygen species. Nitric Oxide 1, 145 (1997).
40. M. Wrona, K. Patel, and P. Wardman, Reactivity of 2′,7′-dichlorodihydrofluorescein and dihydrorhodamine 123 and their oxidized forms toward carbonate, nitrogen dioxide, and hydroxyl radicals. Free Radic. Biol. Med. 38, 262 (2005).
41. A. Bizyukin, L. Korkina, and B. Velichkovskii, Comparative use of 2,7-dichlorofluorescin diacetate, dihydrorhodamine 123, and hydroethidine to study oxidative metabolism in phagocytic cells. Bull. Exp. Biol. Med. 119, 347 (1995).
42. 2 in cultured endothelial cells. Arch. Biochem. Biophys. 302, 348 (1993).
43. H. Sakurada, H. Koizumi, A. Ohkawara, T. Ueda, and N. Kamo, Use of dihydrorhodamine 123 for detecting intracellular generation of peroxides upon UV irradiation in epidermal keratinocytes. Arch. Dermatol. Res. 284, 114 (1992).
44. L. M. Henderson and J. B. Chappell, Dihydrorhodamine 123: A fluorescent probe for superoxide generation? Eur. J. Biochem. 217, 973 (1993).
45. D. Neuman, A. D. Ostrowski, A. A. Mikhailovsky, R. O. Absalonson, G. F. Strouse, and P. C. Ford, Quantum dot fluorescence quenching pathways with Cr(III) complexes. Photosensitized NO production from trans-Cr(cyclam)(ONO)2+. J. Am. Chem. Soc. 130, 168 (2008).
46. R. E. Huie and S. Padmaja, The reaction of no with superoxide. Free Radic. Res. Commun. 18, 195 (1993).
47. H. Maeda and T. Akaike, Nitric oxide and oxygen radicals in infection, inflammation, and cancer. Biochemistry (Mosc.) 63, 854 (1998).
48. C. D. Borsarelli, E. N. Durantini, and N. A. Garcia, Singlet molecular oxygen-mediated photooxidation of nitrophenolic compounds in water-in-oil microemulsions. A kinetic study. J. Chem. Soc. Perkin Trans. 2, 2009 (1996).
49. M. Okamoto, F. Tanaka, and S. Hirayama, High-pressure study on the quenching mechanism by oxygen of the lowest triplet state in solution. J. Phys. Chem. A 102, 10703 (1998).
50. T. Christensen, G. Volden, J. Moan, and T. Sandquist, Release of lysosomal enzymes and lactate dehydrogenase due to hematoporphyrin derivative and light irradiation of NHIK 3025 cells in vitro. Ann. Clin. Res. 14, 46 (1982).
51. K. Berg, P. K. Selbo, L. Prasmickaite, T. E. Tjelle, K. Sandvig, J. Moan, G. Gaudernack, O. Fodstad, S. Kjolsrud, H. Anholt, G. H. Rodal, S. K. Rodal, and A. Hogset, Photochemical internalization: A novel technology for delivery of macromolecules into cytosol. Cancer Res. 59, 1180 (1999).
52. J. Moan, V. Iani, and L. W. Ma, In vivo fluorescence of phthalocyanines during light exposure. J. Photochem. Photobiol. B 42, 100 (1998).
53. J. Silver and W. Ou, Photoactivation of quantum dot fluorescence following endocytosis. Nano Lett. 5, 1445 (2005).
54. A. C. Allison, I. A. Magnus, and M. R. Young, Role of lysosomes and of cell membranes in photosensitization. Nature 209, 874 (1966).
55. A. C. Allison, Role of lysosomes in oxygen toxicity. Nature 205, 141 (1965).
56. Z. Zhelev, R. Jose, T. Nagase, H. Ohba, R. Bakalova, M. Ishikawa, and Y. Baba, Enhancement of the photoluminescence of CdSe quantum dots during long-term UV-irradiation: Privilege or fault in life science research? J. Photochem. Photobiol. B 75, 99 (2004).
57. X. Michalet, F. F. Pinaud, L. A. Bentolila, J. M. Tsay, S. Doose, J. J. Li, G. Sundaresan, A. M. Wu, S. S. Gambhir, and S. Weiss, Quantum dots for live cells, in vivo imaging, and diagnostics. Science 307, 538 (2005).
58. A. M. Derfus, W. C. W. Chan, and S. N. Bhatia, Probing the cytotoxicity of semiconductor quantum dots. Nano Lett. 4, 11 (2004).
59. J. M. Tsay and X. Michalet, New light on quantum dot cytotoxicity. Chem. Biol. 12, 1159 (2005).
60. B. I. Ipe and C. M. Niemeyer, Nanohybrids composed of quantum dots and cytochrome P450 as photocatalysts. Angew. Chem. Int. Ed Engl. 45, 504 (2006).
61. 2 films. J. Am. Chem. Soc. 128, 2385 (2006).
62. V. I. Klimov (ed.), Semiconductor and Metal Nanocrystals: Synthesis and Electronic and Optical Properties, Marcel Dekker, New York, Basel (2003).
63. P. Maestro, M. Chagny, P.-P. Jobert, H. Van Damme, and S. Berthier, Optics. Nanomaterials and Nanochemistry, edited by C. Brechignac, P. Houdy, and M. Lahmani, Springer-Verlag, Belin, Berlin, Heidelberg (2006), pp. 633-659.
64. 2 powder. The Photo-Kolbe decarboxylative route to the breakdown of the benzene ring and to the production to butane. J. Phys. Chem. 85, 218 (1981).
65. K. S. Wissiak, B. Sket, and M. Vrtacnik, Heterogeneous photocatalytic decomposition of halosubstituted benzyl alcohols on semiconductor particles in aqueous media. Chemosphere 41, 1451 (2000).
66. S. J. Clarke, C. A. Hollmann, Z. Zhang, D. Suffern, S. E. Bradforth, N. M. Dimitrijevic, W. G. Minarik, and J. L. Nadeau, Photophysics of dopamine-modified quantum dots and effects on biological systens. Nat. Mater. 5, 409 (2006).
67. B. I. Ipe, M. Lehnig, and C. M. Niemeyer, On the generation of free radical species from quantum dots. Small 1, 706 (2005).
68. A. Anas, H. Akita, H. Harashima, T. Itoh, M. Ishikawa, and V. Biju, Photosensitized breakage and damage of DNA by CdSe-ZnS quantum dots. J. Phys. Chem. B 112, 10005 (2008).
69. 2/DNA nanoconjugates. Chemistry 14, 1492 (2008).
70. C. S. Foote, Definition of Type I and Type II photosensitized oxidation. Photochem. Photobiol. 54, 659 (1991).
71. A. A. Krasnovsky, Jr., Photodynamic action and singlet oxygen. Biophys. (Mosc) 49, 289 (2004).