Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2006-02-28
2006-02-28
Raymond, Richard (Department: 1623)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
C540S123000, C540S125000, C540S128000, C534S015000, C536S029110, C424S009362, C424S009610
Reexamination Certificate
active
07005518
ABSTRACT:
Fluorescent dyes are disclosed which are useful as reporter groups for labeling biomolecules. The silicon phthalocyanine dyes disclosed are preferably water soluble, isomericly pure, possess high quantum yield, and are useful in bioassays.
REFERENCES:
patent: 3094536 (1963-06-01), Kenney
patent: 4997928 (1991-03-01), Hobbs, Jr.
patent: 5135717 (1992-08-01), Renzoni et al.
patent: 5166197 (1992-11-01), Kenney et al.
patent: 5171534 (1992-12-01), Smith et al.
patent: 5332666 (1994-07-01), Prober et al.
patent: 5346670 (1994-09-01), Renzoni et al.
patent: 5403928 (1995-04-01), Arrhenuis
patent: 5484778 (1996-01-01), Kenney et al.
patent: 5846703 (1998-12-01), Devlin et al.
patent: 5872248 (1999-02-01), Cheng et al.
patent: 6027709 (2000-02-01), Little et al.
patent: 6060598 (2000-05-01), Devlin et al.
patent: 6323186 (2001-11-01), Klaubert et al.
patent: 2002/0077487 (2002-06-01), Leung et al.
patent: 1 038 938 (2000-09-01), None
patent: WO 89/09282 (1989-10-01), None
patent: WO 91/11533 (1991-08-01), None
patent: WO 91/18007 (1991-11-01), None
patent: WO 92/03575 (1992-03-01), None
patent: WO 94/05688 (1994-03-01), None
patent: WO 02/24815 (2002-03-01), None
patent: WO 02/096913 (2002-12-01), None
patent: WO 03/082988 (2003-10-01), None
Rywkin, S. et al., “Selective protection against IgG binding to red cells treated with phthalocyanines and red light for viur inactivation”, Transfusion (Malden, MA U.S.) (1995), 35(5), 414-20.
Rywkin, S. et al., “New phthalocyanines for photodynamic virus inactivation in red blood cell concentrates”, Photochemistry & Photobiology (1994), 60(2), 165-70.
Barrel, B., “DNA sequencing: present limitations and prospects for the future” FASEB Journal 5(1):40-45 (1991).
Bruschi, P. et al., “Sensing properties of polypyrrole-polytetrafluoroethylene composite thin films from granular metal-polymer precursors” Sensors and Actuators A 32:313-317 (1992).
Chen, Z. et al., “Monomerization of cationic phthalocyanine in AOT reversed micelles” Langmuir 17:7957-7959 (2001).
De Filippis, M. et al., “Synthesis of a new water-soluble octa-cationic phthalocyanine derivative for PDT” Tetrahedron Lett 41:91 43-9147 (2000).
Esposito, J. et al., “The synthesis and physical properties of some organo- and organosilicon phthalocyanines” Inorganic Chemistry 5(11): 1979-1984 (1979) (Reprinted from 1966).
Hermanson, G.,Bioconjugate Technicues, Pierce Chemical Company, Rockford Illnois, Academic Press, pp. 487-492 (1995).
Hu, M. et al., “Hydroxyphthalocyanines as potential photodynamic agents for cancer therapy” J. Med. Chem. 41:1789-1802 (1998).
Innis M. et al., “DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-simplified DNA” Proc Natl Acad Sci U S A. 85(24):9436-40 (1988).
Jouve, C. et al., “Conductive polyethylene as sensitive layer for gas detection” Sensors and Actuators 6 28:75-80 (1995).
Joyner, R. et al., “Diphenoxysilicon phthalocyanine” J. Inorg. Nucl. Chem. 15:387-388 (1980).
Kasuga, K. et al., “Preparation of unsymmetrical phthalocyanine by means of a ring expansion of subphthalocyanine” Inorganica Chimica Acta 196: 127-128 (1992).
Kimura, M. et al., “Catalytic oxidation of 2-mercaptoethanol by cationic water-soluble phthalocyaninetocobalt(II) complexes” J. Porhyrins and Phthalocyanines 1:309-313 (1997).
Kobayashi, N. et al., “New route to unsymmetrical phthalocyanine analogues by the use of structurally distorted subphthalocyanines” J. Am. Chem. Soc. 112:9640-9641 (1990).
Licha, K. “Contrast agents for optical Imaging”Topics in Current Chemistryvol. 222, Springer-Verlag Berlin Heidelberg, pp. 1-29 (2002).
Lundberg, B. et al., “Resistivity of a composite conducting polymer as a function of temperature, pressure, and environment: Applications as a pressure and gas concentration transducer” J. Appl. Phys. 80(3):1074-1079 (1988).
Maxam, A. et al., “Sequencing end-labeled DNA with base-specific chemical cleavages” Meth. in Enzym. 85:499-560 (1980).
Middendorf, L. et al., “Sequencing Technology” Chapter inBiotechnology, vol. 5b, Genomics and BioinformaticsRehm and Reed (Eds.), Wiley-VCH Publishers, Germany, (2001) ISBN: 3-527-28328-5.
Minnock, A. et al., “Mechanism of uptake of a cationic water-soluble pyridinium zinc phthalocyanine across the outer membrane ofEscherichia coli” Antimicrobial Agents and Chemotherapy 44(3):522-527 (2000).
Minnock, A. et al., “Photoinactivation of bacteria. Use of a cationic water-soluble zinc phthalocyanine to photoinactivate both gram-negative and gram positive bacteria” J. Photochem. Photobiol. B: Biol. 32 (3):159-164 (1996) Abstract Only.
Neuburger, G. et al., “Chemically actuated electronic switch” Sensors and Actuators, 81 326-332 (1990).
Ngai, T. et al., “Disstacking of phthalocyanine in water by poly(ethylene oxide)” Langmuir 17:1381-1383 (2001).
Ruschau, G. et al., “0-3 ceramic/polymer composite chemical sensors” Sensors and Actuators 20:269-275 (1989).
Sanger et al., “DNA sequencing with chain-terminating inhibitors” Proc. Natl. Acad. Sci. USA 74(12):5463-7 (1977).
Sastre, A. et al., “Synthesis of novel unsymmetrically substituted push-pull phthalocyanines” J. Org. Chem. 61(24):8591-8597 (1996).
Sastre, A. et al., “Synthesis of novel unsymmetrical monoaminated phthalocyanines” Tetrahedron Letters 36(48):8501-8504 (1995).
Sharman, W. et al., “Novel water-soluble phthalocyanines substituted with phosphonate moieties on the benzo rings” Tetrahedron Lett. 37(33):5831-5834 (1996).
Stahl, S. et al., “Solid phase DNA sequencing using the biotin-avidin system” Nucleic Acids Res. 16(7):3025-38 (1988).
Tabor, S. et al., “DNA sequence analysis with a modified bacteriophage T7 DNA polymerase” Proc. Natl. Acad. Sci. USA 84:4767-71 (1987).
Trainor, G., “DNA sequencing, automation, and the human genome” Anal. Chem. 62(5):418-428 (1990).
Wang, X. et al., “Synthesis, spectral and aggregation properties of a novel water-soluble tetracarboxynaphthalocyaninatozinc” Dyes and Pigments 41(3):193-198 (1999).
Weber, J. et al., “Complexes derived from strong field ligands. XIX. Magnetic properties of transition metal derivatives of 4,4′,4″,4′″-tetrasulfophthalocyanine” Inorg. Chem. 4(4):469-471 (1965).
Weitemeyer, A. et al., “Unsymmetrically substituted phthalocyanine derivatives via a modified ring enlargement reaction of unsubstituted subphthalocyanine” J. Org. Chem. 60:4900-4904 (1995).
Yang, Y. et al., “Dimerization of cobalt(II) tetrasulfonated phthalocyanine in water and aqueous alcoholic solutions” Inorg. Chem. 24:1765-1769 (1985).
Zaheer, A. et al., “In vivo near-infrared fluorescence Imaging of osteoblastic activity” Nature Biotech. 19:1148-1154 (2001).
Chen Jiyan
Draney Daniel R.
Peng Xinzhan
Li-Cor Inc.
Raymond Richard
Townsend & Townsend & Crew LLP
Ward Paul V.
LandOfFree
Phthalocyanine dyes does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Phthalocyanine dyes, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Phthalocyanine dyes will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3698222