U.S. patents available from 1976 to present.
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Pharmaceutical oral patch for controlled release of pharmaceutical agents in the oral cavity

Patent 6197331 Issued on March 6, 2001. Estimated Expiration Date: Icon_subject July 24, 2017. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3255018

3679792

Dosage form
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Issued on: 08/03/1976
Inventor: Tsuk ,   et al.

Pharmaceutical preparation for oral cavity administration
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Process for preparing a time delayed release flavorant and an improved flavored chewing gum composition
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Composition for periodontal administration
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Inventor: Loesche

Sustained release breath freshener, mouth and palate coolant wafer composition and method of use
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Compositions applied in the mouth
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Issued on: 12/30/1986
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Oral bandage and oral preparations
Patent #: 4772470
Issued on: 09/20/1988
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Inventors

Assignee

Application

No. 899775 filed on 07/24/1997

US Classes:

424/448, Pressure sensitive adhesive means424/443, Web, sheet or filament bases; compositions of bandages; or dressings with incorporated medicaments424/447, Bandages with incorporated medicaments424/449, Transdermal or percutaneous602/3, Protective covering means for a bandage or cast602/41, BANDAGE STRUCTURE604/890.1CONTROLLED RELEASE THERAPEUTIC DEVICE OR SYSTEM

Examiners

Primary: Clardy, S. Mark
Assistant: Williamson, Michael A.

Attorney, Agent or Firm

Foreign Patent References

  • 0 223 245 EP. 05/12/1987
  • 4-38726 JP. 06/12/1992
  • WO 91/19486 WO. 12/12/1991
  • WO 97/02020 WO. 01/12/1997

International Class

A61F 013/02

Abstract

The invention is directed to a controlled-release solid composition for the oral cavity or "pharmaceutical oral patch" that adheres to hard dental surfaces, such as teeth and dentures, and releases an active pharmaceutical agent into the oral cavity. Release of the agent is for a predetermined period of time and at a predetermined sustained concentration. The site of action of the agent is local or systemic.

Other References

  • Alvarez-Fuentes, J. et al., "Morphine Polymeric Coprecipitates for Controlled Release: Elaboration and Characterization," Drug Dev. and Indust. Pharm. 20(15):2409-2424 (1994)
  • Bircher, A.J. et al., "Adverse skin reactions to nicotine in a transdermal therapeutic system," Contact Dermatitis 25(4):230-236 (1991)
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  • Friend, D.R., "Polyacrylate resin microcapsules for taste masking of antibiotics," J. Microencap. 9(4):469-480 (1992)
  • Govender, T. et al., "Microencapsulated Eudragit.RTM. RS30D-coated controlled-release pellets: the influence of dissolution variables and topographical evaluation," J. Microencap. 14(1):1-13 (Jan.-Feb. 1997)
  • Kaura, S. et al., "A Study of the Effects of Sucrose Concentration, Lacquer Concentration and Coating Time on the Formulation of Stable and Effective Carbenicillin Indanyl Sodium Microcapsules," Drug Dev. and Indust. Pharm. 14(7):925-937 (1988)
  • Kim, N.-S. et al., "Preparation and Evaluation of Eudragit Gels. III: Rectal Gel Preparations for Sustained Release of Pentoxifylline," J. Pharm. Sci. 81(6):537-540 (1992)
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  • Morishita, I. et al., "Controlled Release Microspheres Based on Eudragit L100 for the Oral Administration of Erythromycin," Drug Design and Delivery 7(4):309-319 (1991)
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  • Nagai, T., "Buccal/Gingival Drug Delivery Systems," J. Controlled Release 6:353-360 (1987)
  • Narisawa, S. et al., "An Organic Acid-Induced Sigmoidal Release System for Oral Controlled-Release Preparations. 2. Permeability Enhancement of Eudragit RS Coating Led by the Physicochemical Interactions with Organic Acid," J. Pharm. Sci. 85(2):184-188 (Feb. 1996)
  • Ndesendo, V.M.K. et al., "Microencapsulation of chloroquine diphosphate by Eudragit RS100," J. Microencap. 13(1):1-8 (Jan.-Feb. 1996)
  • Prantera, C. et al., "Oral 5-Aminosalicyclic Acid (Asacol) in the Maintenance Treatment of Crohn's Disease," Gastroenterology 103(2):363-368 (1992)
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