EVALUATION OF UV-RADIATION INDUCED SINGLET OXYGEN GENERATION POTENTIAL OF SELECTED DRUGS

REFERENCES

• Xue Y., Nicholson. The Two Major Spore DNA Repair Pathways, Nucleotide Excision Repair and Spore Photoproduct Lyase, are Sufficient for the Resistance of Bacillus subtilis Spores to Artificial UVC and UVB but not in Solar Radiation. Appl. Environ. Microbiol. 1996; 62: 2221–2227
   PubMed Web of Science ®Google Scholar
• Urbach F. Introduction. Biological Responses to UVA Radiation, F. Urbach. Veldenmar Publishing Co., Overlan Park, Kans 1992; 1–6
   Google Scholar
• The Biological Effects of UVA Radiation, F. Urbach, R.W. Gange. Praeger Publishers, New York 1986
   Google Scholar
• Waksman S.A. Microbial Antagonism and Antibiotic Substances. The Commonwealth Fund, New York 1945
   Google Scholar
• Whiteman M., Kaur H., Halliwell B. Protection Against Peroxynitrite Dependent Tyrosine Nitration and Alpha 1-Antiproteinase Inactivation by Some Anti-Inflammatory Drugs and by the Antibiotic Tetracycline. Ann. Rheum. Dis. 1996; 55: 383–387
   PubMed Web of Science ®Google Scholar
• Kochevar I.E., Dunn D.A. Photosensitized Reactions of DNA: Cleavage and Addition. Bioorganic Photochemistry, H. Morrison. John Wiley, New York 1990; Vol.(I): 273
   Google Scholar
• Harber L.C., Bickers D.R. Drug Induced Photosensitivity (Phototoxic and Photoallergic Drug Reactions). Photosensitivity Diseases. B.C. Decker Inc., Toronto 1989; 160
   Google Scholar
• Pathak M.A., Joshi P.C. Production of ROS (1O2 and ) by psoralens and UVR (320–400 nm). Biochim. et Biophys. Acta 1984; 798: 115–126
   PubMed Web of Science ®Google Scholar
• Ray R.S., Mehrotra S., Prakash S., Joshi P.C. UVR Induced Production of Superoxide Radicals by Selected Antibiotics. Drug Chem. Toxicol 1996; 19: 121
   PubMed Web of Science ®Google Scholar
• Akamatsu H., Niwa Y., Sasaki H., Matoba Y., Asada Y., Horio T. Effect of Pyridone Carboxylic Acid Antimicrobials on the Generation of Reactive Oxygen Species in vitro. J. Int. Med. Res. 1996; 24: 345–351
   PubMed Web of Science ®Google Scholar
• Harber L.C., Bickers D.R. Drug Induced Photosensitivity (Phototoxic and Photoallergic Drug Reactions). Photosensitivity Diseases. B.C. Decker Inc., Toronto 1989; 169
   Google Scholar
• Marzulli F.N., Maibach HI. Photoirritation (Phototoxicity, Phototoxic Dermatitis). Dermatotoxicology. Taylor & Francis, USA 1996; 232
   Google Scholar
• Ray R.S., Mehrotra S., Shankar U., Babu S.G., Joshi P.C., Hans R.K. Evaluation of UV-Induced Superoxide Radical Generation Potential of Some Common Antibiotics. Drug Chem. Toxicol 2001; 24(2)191–200
   PubMed Web of Science ®Google Scholar
• Kawamata T., Katayama Y., Maeda T., Mori T., Aoyama M., Kikuchi T., Uwahodo Y. Antioxidant, OPC-14117, Attenuated Edema Formation and Behavioral Deficit Following Cortical Contusion in Rats. Acta. Neurochir. Suppl. Wien. 1997; 70: 191–193
   PubMedGoogle Scholar
• Ramakrishna Rao D.N., Cederbaum A.I. Generation of ROS by the Redox Cycling of Nitropruside. Biochim. Biophys. Acta. 1996; 1289: 195–202
   PubMed Web of Science ®Google Scholar
• Nilsson R., Merkel P.B., Kearns D.R. Unambiguous Evidence for the Participation of Singlet Oxygen in Photodynamic Oxidation of Amino Acids. Photochem. Photobiol. 1972; 16: 117–124
   PubMed Web of Science ®Google Scholar
• Lion Y., Delmelle M., Vorst A.V.de. New Method of Detecting Singlet Oxygen Production. Nature 1976; 263: 442–443
   PubMed Web of Science ®Google Scholar
• Kraljic I., Mohsni E.S. A New Method for the Detection of Singlet Oxygen in Aqueous Solution. Photochem. Photobiol 1978; 28: 577–581
   Web of Science ®Google Scholar
• Lindig B.A., Rodgers M.A.J., Schaap A.P. Determination of the Lifetime of Singlet Oxygen in D2O using 9,10-Anthracenedipropionic Acid, A Water Soluble Probe. J. Am. Chem. Soc. 1980; 102: 5590–5593
   Web of Science ®Google Scholar
• Zhang S.P., Zhao J.Q., Jiang L.J. Photosensitized Formation of 1O2 by Phyco-Biliproteins in Neutral Aqueous Solution. Free Rad. Res. 2000; 33: 489–496
   PubMed Web of Science ®Google Scholar
• Augustin C., Collombel C., Damour O. Use of Dermal Equivalent and Skin Equivalent Models for Identifying Phototoxic Compounds In Vitro. 1997; 13(1–2)27
   Google Scholar
• Joshi P.C. Ultraviolet Radiation Induced Photodegradation and 1O2, O2-Production by Riboflavin, Lumichrome and Lumiflavin. Ind. J. Biochem. Biophys. 1989; 26: 186–189
   PubMed Web of Science ®Google Scholar
• Moore D.E., Hemmens V.J., Vip H. Photosensitization by Drugs: Nalidixic and Oxolinic Acids. Photochem. Photobiol. 1984; 39: 57–61
   PubMed Web of Science ®Google Scholar
• Hasan T., Kochevar I.E., McAuliffe J.D., Cooperman B.S., Abdulah D. Mechanism of Tetracycline Phototoxicity. J. Invest. Dermatol. 1984; 83: 1793
   Web of Science ®Google Scholar
• Li A.S.W., Roethling H.P., Cummings K.B., Chignell C.F. Superoxide Radical Photogenerated from Aqueous Solutions of Tetracycline Antibiotics (pH 7.3) as Evidenced by DMPO Spin Trapping and Cytochrome-C Reduction. Biochem. Biophys. Res. Commun. 1987; 146: 1191
   PubMed Web of Science ®Google Scholar
• Kehrer J.P. Free Radicals as Mediators of Tissue Injury and Disease. Crit. Rev. Toxicol. 1993; 23: 21
   PubMed Web of Science ®Google Scholar
• Gray P.J., Phillips D.R., Wedd A.G. Photosensitized Degradation of DNA by Daunomycin. Photochem. Photobiol. 1982; 36: 49
   PubMed Web of Science ®Google Scholar
• Klecak G., Urbach F., Urwyler H. Fluoroquinolene Antibacterials Enhance UVA-Induced Skin Tumors. J. Photochem. Photobiol. B. 1997; 37: 174
   PubMed Web of Science ®Google Scholar
• Traynor N.J., Barratt M.D., Lovell W.W., Ferguson J., Gibbs N.K. Comparison of an In Vivo Cellular Phototoxicity Model Against Controlled Clinical Trials of Fluoroquinolene Skin Phototoxicity. Toxicol. In Vitro 2000; 14: 275
   PubMed Web of Science ®Google Scholar
• Novelli E.L., Silva A.M., Novelli J.L., Curi P.R. Reactive Oxygen Generation by Azomethine-H: A New Antimalarial Drug. Can. J. Physiol. Pharmacol. 1995; 73: 1189
   PubMed Web of Science ®Google Scholar
• Nohi H., Gille L., Staniek K. The Exogenous NADH Dehydrogenase of Heart Mitochondria is the Key Enzyme Responsible for Selective Cardiotoxicity of Anthracyclines. z-Naturforsch-C. 1998; 53: 279
   PubMed Web of Science ®Google Scholar
• Maeda H. Recent Advances in Research on SMANCS. Can. To. Kagaku, Ryoho. 1998; 25: 1
   PubMedGoogle Scholar
• Grzelak A., Rychlik B., Bartosz G. Light Dependent Generation of ROS in Cell Culture Media. Free Radical Biology and Medicine 2001; 30(12)1418–1425
   PubMed Web of Science ®Google Scholar
• Ouannes C., Wilson T. Quenching of 1O2 by Tertiary Aliphatic Amines, Effects of DABCO. J. Am. Chem. Soc. 1968; 90: 6527–6528
   Web of Science ®Google Scholar
• Foote C.S., Fugimoto T.T., Chang Y.C. Chemistry of Singlet Oxygen. XV. Irrelevance of Azide Trapping to Mechanism of the ene Reaction. Tetrahedron Lett. 1972; 45–48
   Web of Science ®Google Scholar
• Zhai X., Muhammad A. Direct Detection and Quantification of 1O2 During Ischemia and Reperfusion in Rat Hearts. Am. J. Physiol. 1995; 269: H 1229–H 1236
   Google Scholar
• Stratton S.P., Schaefer W.H., Liebler D.C. Isolation and Identification of 1O2 Oxidation Products of β-Carotene. Chem. Res. Toxicol. 1993; 6: 542–547
   PubMed Web of Science ®Google Scholar
• Joshi P.C., Pathak M.A. The Role of Active Oxygen (1O2 and ) Induced by Crude Coal Tar and Its Ingrediant Used in Photochemotherapy of Skin Diseases. The J. of Invest. Dermatol. 1984; 82: 67–73
   PubMed Web of Science ®Google Scholar
• Srivastava L.P., Mishra R.B., Joshi P.C. Photosensitizing Potential of Benzanthrone. Food Chem. Toxicol. 1990; 28(9)653–658
   PubMed Web of Science ®Google Scholar
• Pathak M.A. Molecular Aspects of Drug Photosensitivity with Special Emphasis on Psoralen Sensitization Reactions. J. Natl. Cancer Inst. 1982; 69: 163–170
   PubMed Web of Science ®Google Scholar
• Pathak M.A., Kramer D.M. Photosensitization of Skin In Vivo by Furocoumarins (psoralens). Biochem. Biophys. Acta 1969; 195: 197–206
   PubMed Web of Science ®Google Scholar
• Tanielian C., Schweitzer C., Mechin R., Wolff C. Quantum Yield of Singlet Oxygen Production by Monomeric and Aggregated Forms of Hematoporphyrin Derivative. Free Rad. Biol. Med. 2001; 30(2)208–212
   PubMed Web of Science ®Google Scholar
• Joshi P.C. Comparison of the DNA-Damaging Property of Photosensitized Riboflavin Via Singlet Oxygen and Superoxide Mechanisms. Toxicol. Lett. 1985; 26: 211–217
   PubMed Web of Science ®Google Scholar
• Suzuki Y., Miura T., Ogiso T. Riboflavin Photosensitized Hemolysis of Rat Erythrocytes in the Presence of Serum. J. Pharmacobiodyn. 1982; 5: 568–575
   PubMedGoogle Scholar
• Goosey J.D., Zigler J.S., Kinoshita J.H. Cross-Linking of Lens Crystallins in a Photodynamic System: A Process Mediated by Singlet Oxygen. Science 1980; 208: 1278–1280
   PubMed Web of Science ®Google Scholar