Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2006-12-05
2006-12-05
Wilson, James O. (Department: 1623)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Heterocyclic carbon compounds containing a hetero ring...
C514S191000, C514S163000, C514S410000, C540S128000, C540S123000, C540S140000, C540S125000, C536S029110
Reexamination Certificate
active
07144879
ABSTRACT:
The present invention is directed to metal-phthalocyanines of general formula (I) to the corresponding conjugates, the processes for their preparation and use in the photodynamic therapy of microbial infections (viral, bacterial and mycotic), tumor, pre-cancerous and proliferative pathologies and/or in the diagnosis, as well as for blood and blood derivatives sterilization
REFERENCES:
patent: 0 906 758 (1999-04-01), None
patent: 0906758 (1999-04-01), None
Ben-Hur et al., “The Phthalocyanines: A New Class of Mammalian Cells Photosensitizers With a Potential for Cancer Phototherapy,”Int. J. Radiat. Biol., 47(2):145-147 (1985).
Gomer, “Photodynamic Therapy in the Treatment of Malignancies,”Seminars in Hematology, 26(1):27-34 (1989).
Jori, “Tumour Photosensitizers: Approaches to Enhance the Selectivity and Efficiency of Photodynamic Therapy,”J. Photochem. Photobiol. B: Biology, 36:87-93 (1996).
Brasseur et al., “Biological Activities of Phthalocyanines—V. Photodynamic Therapy of EMT-6 Mammary Tumors in Mice With Sulfonated Phthalocyanines,”Photochem. Photobiol., 45(5):581-586 (1987).
Brasseur et al., “Biological Activities of Phthalocyanines—VII. Photoinactivation of V-79 Chinese Hamster Cells by Selectively Sulfonated Gallium Phthalocyanines,”Photochem. Photobiol., 46(5):739-744 (1987).
Paquette et al., “Biological Activities of Phthalocyanines—VIII. Cellular Distribution in V-79 Chinese Hamster Cells and Phototoxicity of Selectively Sulfonated Aluminum Phthalocyanines,”Photochem. Photobiol., 47(2):215-230 (1988).
Brasseur et al., “Biological Activities of Phthalocyanines—IX. Photosensitization of V-79 Chinese Hamster Cells and EMT-6 Mouse Mammary Tumor by Selectively Sulfonated Zinc Phthalocyanines,”Photochem. Photobiol., 47(5):705-711 (1988).
Margaron et al., “Structure-Photodynamic Activity Relationships of a Series of 4-Substituted Zinc Phthalocyanines,”Photochem. Phitobiol., 63(2):217-223 (1996).
Paquette et al., “Phthalocyanines Pour la Thérapie Photocynamique du Cancer: Effet des Substituants Tertio-Butyles sur l'accumulation cellulaire et l'activité Photodynamique de Phthalocyanines Sulfonées de Gallium,”J. Chim. Phys., 88:1113-1123 (1991), abstract.
Gaspard, “A New Method for the Synthesis of Zinc Tetrakis-(3-methylpyridyloxy)-phthalocyanine and the Physical Properties of—Dimers Formed by Complexation of the Cationic Phthalocyanine with Anionic Porphyrins,”J. Chem. Soc. Perkin Trans. II, 383-389 (1989).
Siegl, “Metal-Chelating 1,3-bis(2′Pyridylimino)isoindolines,”J. Heterocyclic Chem., 18:1613-1618 (1981).
Wöhrle et al., “A Simple Synthesis of 4,5-Disubstituted 1,2-Dicyanobenzes and 2,3,9,10,16,17,23,24-Octasubstituted Phthalocyanines,”Synthesis2:194-196 (1993).
Kaninskii et al., “Substitution of the Nitro Group in 4-Nitrophthalonitrile with the Phenol-Metal Carbonate System as Nucleophile,”Journal of Organic Chemistry of the USSR, 38:964-967 (1992).
Mikhalenko et al., “Phthalocyanines and Related Compounds. XIX. Tetra- and Octaamino-Substituted Phthalocyanines,”Journal of Chemistry, 51(7):1405-1411 (1981).
Haworth et al., “Some Green Pigments of the Phthalocyanine Series,”Chemical Abstracts, 39(20), Abstract No. 4610 (1945).
Freccero et al., “Photochemical Reaction of Phthalimides and Dicyanophtalimides with Benzylic Donors,”J. Org. Chem., 58:1740-1745 (1993).
Gracheva et al., “Preparation of 1,2,3,4-tetrahydroquinoline Derivatives,” Caplus Online Chemical Abstracts Service, Abstract No. 108:204512 (1987).
De Filippis Maria Paola
Dei Donata
Fantetti Lia
Jori Giulio
Roncucci Gabrio
L. Molteni & C. Dei Fratelli
Lindeman Jeffrey A.
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