Patents by Inventor F. Donald Roberts
F. Donald Roberts has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).
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Patent number: 7033608Abstract: Novel burst-free, sustained release biocompatible and biodegrable microcapsules which can be programmed to release their active core for variable durations ranging from 1–100 days in an aqueous physiological environment. The microcapsules are comprised of a core of polypeptide or other biologically active agent encapsulated in a matrix of poly(lactide/glycolide) copolymer as a blend of uncapped (free carboxyl end group) and end-capped forms ranging in ratios from 100/0 to 1/99.Type: GrantFiled: June 22, 1999Date of Patent: April 25, 2006Assignee: The United States of America as represented by the Secretary of the ArmyInventors: Ramasubbu Jevanthi, John E. Van Hamont, Phil Friden, Robert H. Reid, F. Donald Roberts, Charles E. McQueen, Jean A. Setterstrom
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Patent number: 6902743Abstract: Novel burst-free, sustained release biocompatible and biodegrable microcapsules which can be programmed to release their active core for variable durations ranging from 1-100 days in an aqueous physiological environment. The microcapsules are comprised of a core of polypeptide or other biologically active agent encapsulated in a matrix of poly(lactide/glycolide) copolymer having a molar composition of lactide/glycolide from 90/10 to 40/60, which may contain a pharmaceutically-acceptable adjuvant, as a blend of uncapped free carboxyl end group and end-capped forms ranging to ratios from 100/0 to 1/99.Type: GrantFiled: April 6, 1998Date of Patent: June 7, 2005Assignee: The United States of America as represented by the Secretary of the ArmyInventors: Jean A. Setterstrom, Thomas R. Tice, Elliot Jacob, Robert H. Reid, John van Hamont, Edgar C. Boedecker, Ramassubbu Jeyanthi, Phil Friden, F. Donald Roberts, Charles E. McQueen, Apurba Bhattacharjee, Alan Cross, Jerald Sadoff, Wendell Zollinger
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Patent number: 6844010Abstract: Novel burst-free, sustained release biocompatible and biodegrable microcapsules which can be programmed to release their active core for variable durations ranging from 1-100 days in an aqueous physiological environment. The microcapsules are comprised of a core of polypeptide or other biologically active agent encapsulated in a matrix of poly(lactide/glycolide) copolymer, which may contain a pharmaceutically-acceptable adjuvant, as a blend of upcapped free carboxyl end group, and end-capped forms ranging in ratios from 100/0 to 1/99.Type: GrantFiled: July 18, 2000Date of Patent: January 18, 2005Assignee: The United States of America as represented by the Secretary of the ArmyInventors: Jean A. Setterstrom, John E. Van Hamont, Robert H. Reid, Elliot Jacob, Ramasubbu Jeyanthi, Edgar C. Boedeker, Charles E. McQueen, Daniel L. Jarboe, Frederick Cassels, William Brown, Curt Thies, Thomas R. Tice, F. Donald Roberts, Phil Friden
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Patent number: 6531573Abstract: Substantially pure peptides containing between 13 and 20 amino acids, inclusive, having the amino acid sequence: R1-R2-R3-R4-R5-R6-R7-R8-R9-R10-R11-R12-R13-R14-R15-R16-R17-R18-R19-R20-R21-R22-R23, where R1 is Asp or is absent; R2 is Ser or is absent; R3 is His or is absent; R4 is Ala; R5 is Lys, Gln, Arg, or another basic amino acid; R6 is Arg, Gln, Lys, or another basic amino acid; R7 is His, Phe, Tyr, Leu, or another hydrophobic amino acid; R8 is His, Phe, Tyr, Leu, or another hydrophobic amino acid; R9 is Gly, Lys, Arg, or another basic amino acid; R10 is Tyr; R11 is Lys, His, Phe, or another hydrophobic amino acid; R12 is Arg, Gln, Lys, or another basic amino acid; R13 is Lys, Gln, Arg, another basic amino acid, or is absent; R14 is Phe or is absent; R15 is His, Phe, Tyr, Leu, another hydrophobic amino acid, or is absent; R16 is Glu or is absent; R17 is Lys or is absent; R18 is His or is absent; R19 is His or is absent; R20 is Ser or is absent; R21 is His or is absent; R22 is Arg or is absent; and R23 isType: GrantFiled: December 18, 1997Date of Patent: March 11, 2003Assignees: Trustees of Boston University, Periodontix, Inc.Inventors: Frank G. Oppenheim, Tao Xu, F. Donald Roberts, Peter Spacciapoli, Phillip M. Friden
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Patent number: 6309669Abstract: Novel burst-free, sustained release biocompatible and biodegrable microcapsules which can be programmed to release their active core for variable durations ranging from 1-100 days in an aqueous physiological environment. The microcapsules are comprised of a core of polypeptide or other biologically active agent encapsulated in a matrix of poly(lactide/glycolide) copolymer, which may contain a pharmaceutically-acceptable adjuvant, as a blend of upcapped free carboxyl end group and end-capped forms ranging in ratios from 100/0 to 1/99.Type: GrantFiled: January 27, 1997Date of Patent: October 30, 2001Assignee: The United States of America as represented by the Secretary of the ArmyInventors: Jean A. Setterstrom, John E. Van Hamont, Robert H. Reid, Elliot Jacob, Ramasubbu Jeyanthi, Edgar C. Boedeker, Charles E. McQueen, Daniel L. Jarboe, Frederick Cassels, William Brown, Curt Thies, Thomas R. Tice, F. Donald Roberts, Phil Friden
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Patent number: 6153210Abstract: Periodontal disease can be treated by the administration of metal ions, preferably silver ions, to the site where the microorganisms that cause this disease reside. Administration can be to periodontal pockets or adjacent to exposed tooth roots or alveolar bone during periodontal surgical procedures. The metal ions can be administered in polymeric microparticles, deformable films or microparticles embedded within deformable films. The metal ions are particularly microbiocidal to the bacterial pathogens that are the causative agents of periodontal disease.Type: GrantFiled: August 14, 1997Date of Patent: November 28, 2000Assignee: Periodontix, Inc.Inventors: F. Donald Roberts, Phillip M. Friden, Peter Spacciapoli, Eric Nelson
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Patent number: 5912230Abstract: Histatin-based peptides representing defined portions of the amino acid sequences of naturally occurring human histatins and methods for treatment of fungal or bacterial infection are described. These histatin-based peptides represent the active anti-fungal and anti-bacterial region of naturally occurring human histatins.Type: GrantFiled: March 11, 1998Date of Patent: June 15, 1999Assignees: Periodontix, Inc., Trustees of Boston UniversityInventors: Frank G. Oppenheim, Tao Xu, F. Donald Roberts, Peter Spacciapoli, Phillip M. Friden
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Patent number: 5885965Abstract: D-amino acid histatins and histatin-based peptides and methods for treatment of fungal or bacterial infection are described. These D-amino acid histatins and histatin-based peptides are longer-acting anti-fungal or anti-bacterial agents than their L-enantiomeric analogues.Type: GrantFiled: March 12, 1998Date of Patent: March 23, 1999Assignees: Periodontix, Inc., Trustees of Boston UniversityInventors: Frank G. Oppenheim, Tao Xu, F. Donald Roberts, Peter Spacciapoli, Phillip M. Friden
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Patent number: 5631228Abstract: Histatin-based peptides representing defined portions of the amino acid sequences of naturally occurring human histatins and methods for treatment of fungal or bacterial infection are described. These histatin-based peptides represent the active anti-fungal and anti-bacterial region of naturally occurring human histatins.Type: GrantFiled: June 7, 1995Date of Patent: May 20, 1997Assignees: Periodontix, Inc., The Trustees of Boston UniversityInventors: Frank G. Oppenheim, Tao Xu, F. Donald Roberts
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Patent number: 5422382Abstract: Substituted xanthene compounds are described which are capable of functioning as absorbers in high intensity light protective compositions and in materials used to prevent the transmission of high intensity light at selected wavelengths. Also described are high intensity light protective compositions containing an effective amount of a substituted xanthene compound and a polymeric compound and a material which prevents transmission of high intensity light at wavelengths between about 482 to about 556 nanometers. The material of this invention can be used to make protective eyewear, optical filters, shields for protecting a persons body from high intensity light, or shields for protecting components of an optical instrument from high intensity light.Type: GrantFiled: June 16, 1992Date of Patent: June 6, 1995Assignee: Steadfast, IncorporatedInventors: Louis Locatell, Kenneth Norland, F. Donald Roberts, Charles Zepp
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Patent number: 5149830Abstract: Substituted xanthene compounds are described which are capable of functioning as absorbers in high intensity light protective compositions and in materials used to prevent the transmission of high intensity light at selected wavelengths. Also described are high intensity light protective compositions containing an effective amount of a substituted xanthene compound and a polymeric compound and a material which prevents transmission of high intensity light at wavelengths between about 482 to about 556 nanometers. The material of this invention can be used to make protective eyewear, optical filters, shields for protecting a persons body from high intensity light, or shields for protecting components of an optical instrument from high intensity light.Type: GrantFiled: February 23, 1990Date of Patent: September 22, 1992Assignee: Steadfast, Inc.Inventors: Louis Locatell, Kenneth Norland, F. Donald Roberts, Charles Zepp