Compositions comprising a UV-absorbing chromophore

Drug – bio-affecting and body treating compositions – Topical sun or radiation screening – or tanning preparations

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

Reexamination Certificate

active

07727514

ABSTRACT:
A chemical composition comprising a linker agent and a compound comprising at least one UV-absorbing chromophore, wherein the linker agent is characterized by the general formula:wherein X1and X2are the same or different, and at least one of X1or X2is a functional group that bonds with the compound comprising at least one UV-absorbing chromophore, and b+f≧2, Y comprises an O, N, or S that is substituted or unsubstituted, each a, b, c, e and f is ≧0 and a+b+c+e+f≧2, d is 0 or 1, n1 and n2 represent the number of hydrogen atoms required to complete the undesignated valencies, and m ranges from 1 to about 100 and each individual m unit may be the same or different.

REFERENCES:
patent: 3153659 (1964-10-01), King
patent: 5155244 (1992-10-01), Greene et al.
patent: 5380890 (1995-01-01), Greene et al.
patent: 5614648 (1997-03-01), Greene et al.
patent: 5683683 (1997-11-01), Scafidi
patent: 5817299 (1998-10-01), Manirazman
patent: 5902591 (1999-05-01), Herstein
patent: 6013270 (2000-01-01), Hargraves et al.
patent: 6346236 (2002-02-01), Compton et al.
patent: 6372234 (2002-04-01), Deckers et al.
patent: 6565865 (2003-05-01), Bekele
patent: 6890520 (2005-05-01), Taniguchi et al.
patent: 2004/0258635 (2004-12-01), Harry-O'kuru
patent: 2004/0258743 (2004-12-01), Compton et al.
patent: 2005/0096340 (2005-05-01), Zhang et al.
patent: 2007/0077636 (2007-04-01), Laszlo et al.
patent: 2008/0050321 (2008-02-01), DeFilippi et al.
patent: WO 9533706 (1995-12-01), None
patent: WO 01/72683 (2001-10-01), None
patent: 2007041424 (2007-04-01), None
patent: 2008003090 (2008-01-01), None
patent: 2008003090 (2008-01-01), None
Hatfield, Ronald D., et al., “Synthesis of Methyl 5-O-trans-Feruloyl-α-L-arabinofuranoside and its Use as a Substrate to Assess Feruloyl Esterase Activity,” Analytical Biochemistry, vol. 194, Academic Press, Inc., 1991, pp. 25-33.
Helm, Richard F., et al., “Synthesis of feruloylated and p-coumaroylated methyl glycosides,” Carbohydrate Research, vol. 229, Elsevier Science Publishers, 1992, pp. 183-194.
Lu, Fachuang, et al., “Facile Synthesis of 4-Hydroxycinnamyl p-Coumarates,” J. Agric. Food Chem., vol. 46, No. 8, American Chemical Society, 1998, pp. 2911-2913.
Compton, David L., et al., “Lipase-Catalyzed Synthesis of Ferulate Esters,” JAOCS, vol. 77, No. 5, 2000, pp. 513-519.
Laszlo, Joseph A., et al., “Packed-bed bioreactor synthesis of feruloylated monoacyl- and diacylglycerols: clean production of a “green” sunscreen,” Green Chemistry, vol. 5, The Royal Society of Chemistry, 2003, pp. 382-386.
Office Action dated Feb. 5, 2008 (13 pages), U.S. Appl. No. 11/425,096, filed Jun. 19, 2006.
Torres, Carlos F., et al., “Lipase-catalyzed synthesis of designer acyl-glycerols rich in residues of eicosapentaenoic, docosahexaenoic, conjugated linoleic, and/or stearic acids,” Eur. J. Lipid Sci. Technol., 2003, pp. 614-623, vol. 105, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Batovska, Daniela I., et al., “Synthesis of Some Phenylpropanoid Monoglycerides via the Mitsunobu Protocol,” Molecules, vol. 10, 2005, pp. 552-558.
Cooper, Raymond, et al., “New Phenolic Diglycerides from ‘Aegilops ovata’,” Phytochemistry, vol. 17, 1978, pp. 1673-1675.
Guyot, B., et al., “Esterification of phenolic acids from green coffee with an immobilized lipase fromCandida antarcticain solvent-free medium,” Biotechnology Letters, vol. 19, No. 6, Jun. 1997, Chapman & Hall, pp. 529-532.
Jang, Dae Sik, et al., “Constituents ofAsparagus officinalisEvaluated for Inhibitory Activity against Cyclooxygenase-2,” Journal of Agricultural Food Chemistry, vol. 52, 2004, pp. 2218-2222.
Laszlo, Joseph A., et al., “Packed-bed bioreactor synthesis of feruloylated monoacyl- and diacylglycerols: clean production of a “green” sunscreen,” Green Chemistry, vol. 5, 2003, The Royal Society of Chemistry, pp. 382-386.
Laszlo, Joseph, et al., “Enzymatic glycerolysis and transesterification of vegetable oil for enhanced production of feruloylated glycerols,” Database Biosis [Online], Sep. 2006, Biosciences Information Service, Philadelphia, PA, US, XP002415387.
Mimaki, Yoshihiro, et al., “Steroidal Saponins from the Bulbs ofLilium brownii,” Phytochemistry, vol. 29, No. 7, 1990, Pergamon Press plc, pp. 2267-2271.
Safari, Mohammad, et al., “Enzymatic synthesis of structured phenolic lipids by incorporation of selected phenolic acids into triolein,” Database Biosis [Online], Jul.-Aug. 2006, Biosciences Information Service, Philadelphia, PA, US, XP002415385.
Tsuchiyama, Moriyasu, et al., “Esterification of ferulic acid with polyols using a ferulic acid esterase fromAspergillus niger,” Database Biosis [Online], Jul. 2006, Biosciences Information Service, Philadelphia, PA, US, XP002415386.
Warner, K., et al., “Addition of ferulic acid, ethyl ferulate, and feruloylated monoacyl- and diacylglycerols to salad oils and frying oils,” Abstract, Journal of American Oil Chemists' Society, vol. 82, No. 9., Sep. 2005, http://www.springerlink.com/content/g0gh57j04431p185/?p=65b97bb125a04aefa0858bf5fd8... (Jan. 16, 2007), XP002415372.
Foreign communication from a related counterpart application—International Search Report & Written Opinion, PCT/US2006/038300, Feb. 7, 2007, 17 pages.
Foreign communication from a related counterpart application—International Search Report, PCT/US07/72557, Feb. 27, 2008, 3 pages.
Lin, Fu-Hsiung, “Ferulic acid stabilizes a solution of vitamins C and E and doubles its photoprotection of skin,” The Journal of Investigative Dermatology, 2005, pp. 826-832, vol. 125, The Society for Investigative Dermatology, Inc.
Office Action dated Jul. 28, 2008 (7 pages), U.S. Appl. No. 11/425,096, filed Jun. 19, 2006.
Office Action (Final) dated Jan. 8, 2009 (11 pages), U.S. Appl. No. 11/425,096, filed Jun. 19, 2006.
Holser, R. A., et al., “Preparation and characterization of 4-methoxy cinnamoyl glycerol,” J Am Oil Chem Soc, 2008, pp. 347-351, vol. 85, AOCS.
Holser, Ronald A., “Kinetics of cinnamoyl glycerol formation,” J Am Oil Chem Soc, 2008, pp. 221-225, vol. 85, AOCS.
Sabally, Keeba, et al., “Lipase-catalyzed transesterification of dihydrocaffeic acid with flaxseed oil for the synthesis of phenolic lipids,” Journal of Biotechnology, 2006, pp. 167-176, vol. 127, Elsevier B.V.
Sun, Shangde, et al., “A novel, two consecutive enzyme synthesis of feruloylated monoacyl- and diacyl-glycerols in a solvent-free system,” Biotechnol Lett, 2007, pp. 1947-1950, Springer Science+Business Media B.V.
Sun, Shangde, et al., “Solvent-free enzymatic synthesis of feruloylated diacylglycerols and kinetic study,” Journal of Molecular Catalysis B: Enzymatic, 2007, pp. 1-20 plus 1 publication disclosure page.
Sun, Shangde, et al., “Solvent-free synthesis of glyceryl ferulate using a commercial microbial lipase,” Biotechnol Lett, 2007, pp. 945-949, Springer Science+Business Media B.V.
Tsuchiyama, Moriyasu, et al., “Esterification of ferulic acid with polyols using a ferulic acid esterase fromAspergillus niger,” Biochimica et Biophysica Acta, 2006, pp. 1071-1079, vol. 1760, Elsevier B.V.
Xin, Jia-Ying, et al., “Lipase-catalyzed synthesis of ferulyl oleins in solvent-free medium,” Food Chemistry, 2009, pp. 640-645, vol. 112, Elsevier Ltd.
Office Action dated Feb. 20, 2000 (21 pages), U.S. Appl. No. 11/771,843, filed Jun. 29, 2007.
Notice of Allowance dated May 1, 2009 (8 pages), U.S. Appl. No. 11/425,096, filed Jun. 19, 2006.
Foreign communication from a related counterpart application—International Preliminary Examination Report, PCT/US07/72557, Oct. 7, 2009, 12 pages.
Office Action (Final) dated Sep. 1, 2009 (37 pages), U.S. Appl. No. 11/771,843, filed Jun. 29, 2007.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Compositions comprising a UV-absorbing chromophore does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Compositions comprising a UV-absorbing chromophore, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Compositions comprising a UV-absorbing chromophore will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-4240249

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.