Combined Action of Phthalocyanine Photosensitization and Gamma-radiation on Mammalian Cells

References

• Bellnier D.A., Dougherty T.J. Haematoporphyrin derivative photosensitization and γ-radiation damage interaction in Chinese hamster ovary fibroblasts. International Journal of Radiation Biology 1986; 50: 659–664
   Google Scholar
• Ben-Hur E. Photochemistry and photobiology of phthalocyanines: new photosensitizers for photodynamic therapy of cancer. Photobiochemistry and Photobiophysics 1987; 407–420, Suppl.
   Google Scholar
• Ben-Hur E., Rosenthal I. The phthalocyanines; a new class of mammalian cells photosensitizers with a potential for cancer phototherapy. International Journal of Radiation Biology 1985a; 47: 145–147
   Google Scholar
• Ben-Hur E., Rosenthal I. Factors affecting the photokilling of cultured Chinese hamster cells by phthalocyanines. Radiation Research 1985b; 103: 403–409
   PubMedGoogle Scholar
• Ben-Hur E., Rosenthal I. Photosensitization of Chinese hamster cells by water soluble phthalocyanines. Photochemistry and Photobiology 1986; 43: 615–619
   PubMed Web of Science ®Google Scholar
• Ben-Hur E., Rosenthal I., Bown S.G., Phillips D. The phthalocyanines: sensitizers with potential for photodynamic therapy of cancer. Photomedicine, E. Ben-Hur, I. Rosenthal. CRC Press, Boca Raton, FL 1987a; 3: 1–17
   Google Scholar
• Ben-Hur E., Fujihara T., Suzuki F., Elkind M.M. Genetic toxicology of the photosensitization of Chinese hamster cells by phthalocyanines. Photochemistry and Photobiology 1987b; 45: 227–230
   PubMedGoogle Scholar
• Ben-Hur E., Elkind M.M., Bronk B.V. Thermally enhanced radioresponse of cultured Chinese hamster cells: inhibition of repair of sublethal damage and enhancement of lethal damage. Radiation Research 1974; 58: 38–51
   PubMed Web of Science ®Google Scholar
• Brasseur N., Ali H., Autenrieth D., Langlois R., van Lier J.E. Biological activities of phthalocyanines—III. Photoinactivation of V79 Chinese hamster cells by tetrasulfophthalocyanines. Photochemistry and Photobiology 1985; 42: 515–512
   PubMedGoogle Scholar
• Chan W.S., Svensen R., Phillips D., Hart I.R. Cell uptake, distribution and response to aluminium chloro sulphonated phthalocyanines, a potential antitumor photosensitizer. British Journal of Cancer 1986; 53: 255–263
   PubMed Web of Science ®Google Scholar
• Countryman P.I., Heddle J.A. The production of micronuclei from chromosome aberration in irradiated cultures of human lymphocytes. Mutation Research 1976; 41: 321–332
   PubMed Web of Science ®Google Scholar
• Dewey W.C., Furman S.C., Miller H.H. Comparison of lethality and chromosomal damage induced by γ-ray in synchronized Chinese hamster cells in vitro. Radiation Research 1970; 43: 561–581
   PubMed Web of Science ®Google Scholar
• Dougherty T.J. Photodynamic therapy (PDT) of malignant tumors. CRC Critical Reviews in Oncology/Hematology 1984; 2: 83–116
   PubMed Web of Science ®Google Scholar
• Elkind M.M., Whitmore G.F. The Radiobiology of Cultured Mammalian Cells. Gordon and Breach, New York 1967; 40–45
   Google Scholar
• Fenech M., Morley A.A. Cytokinesis-block micronucleus method in human lymphocytes: effect of in vivo ageing and low dose x-irradiation. Mutation Research 1986; 161: 193–198
   PubMed Web of Science ®Google Scholar
• Gumrich K., Virssik-Peuckert R.P., Harder D. Temperature and the formation of radiation induced chromosome aberrations. I. The effect of irradiation temperature. International Journal of Radiation Biology 1986; 49: 655–672
   Google Scholar
• Hogstedt B. Micronuclei in lymphocytes with preserved cytoplasm. A method for assessment of cytogenetic damage in man. Mutation Research 1984; 130: 63–72
   PubMedGoogle Scholar
• Kol R., Ben-Hur E., Riklis E., Marko R., Rosenthal I. Photosensitized inhibition of mitogenic stimulation of human lymphocytes by aluminium phthalocyanine tetrasulfonate. Lasers in Medical Sciences, 1: 187–192
   Google Scholar
• Kostron H., Swartz M.R., Miller D.C., Mortuza R.L. The interaction of hematoporphyrin derivative, light and ionizing radiation in a rat glioma model. Cancer 1986; 57: 964–970
   PubMed Web of Science ®Google Scholar
• Moser F.H., Thomas A.C. The Phthalocyanines. CRC Press, Boca Raton, FL 1983; 1: 40–41
   Google Scholar
• Rosenthal I., Kirshna C.M., Riesz P., Ben-Hur E. The role of molecular oxygen in photodynamic effects of phthalocyanines. Radiation Research 1986; 107: 136–142
   PubMed Web of Science ®Google Scholar
• Scott D., Fox M., Fox B.W. The relationship between chromosomal aberrations, survival and DNA repair in tumor cell lines of differential sensitivity to γ-rays and sulphur mustard. Mutation Research 1974; 22: 207–221
   PubMed Web of Science ®Google Scholar
• Selman S.H., Kreimer-Birnbaum M., Chaudhuri K., Garbo G.M., Seaman D.A., Keck R.W., Ben-Hur E., Rosenthal I. Photodynamic treatment of transplantable bladder tumors in rodents after pretreatment with chloroaluminum tetrasulfophthalocyanine. Journal of Urology 1986; 136: 141–145
   PubMedGoogle Scholar
• Spikes J.D. Phthalocyanines as photosensitizers in biological systems and for the photodynamic therapy of tumors. Photochemistry and Photobiology 1986; 43: 691–699
   PubMed Web of Science ®Google Scholar
• Waldow S.M., Hendrson B.W., Dougherty T.J. Enhanced tumor control following sequential treatments of photodynamic therapy (PDT) and localized microwave hyperthermia in vivo. Lasers in Surgery and Medicine 1984; 4: 49–85
   Google Scholar
• Wilson B.C., Jeeves W.P. Photodynamic therapy of cancer. Photomedicine, E. Ben-Hur, I. Rosenthal. CRC Press, Boca Raton, FL 1987; 2: 127–177
   Google Scholar
• Zuk M.M., Tyczkowska K., Ben-Hur E., Newman H.C., Crane S.W., Rosenthal I. Reversed phase liquid chromatographic determination of chloroaluminium phthalocyanine tetrasulfonate in canine serum, tissues and urine. 1988, To be published
   Google Scholar