The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Mar. 07, 2017

Filed:

Dec. 10, 2012
Applicant:

Adhesives Research, Inc., Glen Rock, PA (US);

Inventors:

Scott D. Barnhart, Glen Rock, PA (US);

Andrew P. Full, Glen Rock, PA (US);

Cathy M. Moritz, Glen Rock, PA (US);

Assignee:

Adhesives Research, Inc., Glen Rock, PA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 47/38 (2006.01); A61K 8/73 (2006.01); A61K 9/00 (2006.01); A61K 47/36 (2006.01); G01N 33/543 (2006.01); G01N 33/76 (2006.01);
U.S. Cl.
CPC ...
A61K 47/38 (2013.01); A61K 8/731 (2013.01); A61K 9/006 (2013.01); A61K 47/36 (2013.01); G01N 33/543 (2013.01); G01N 33/76 (2013.01);
Abstract

The invention provides disintegratable films containing a mixture of high molecular weight and low molecular weight water soluble components; and a pharmaceutically or cosmetically active ingredient. Optionally, the films contain a starch component, a glucose component, a filler, a plasticizer and/or humectant. The films are preferably in the form of a mucoadhesive monolayer having a thickness sufficient to rapidly disintegrate in the oral environment and release the active ingredient without undue discomfort to the oral mucosa. The monolayer can be cut to any desired size or shape to provide conveniently useable unit dosage forms for administration to oral or other mucosal surfaces for human pharmaceutical, cosmetic, or veterinary applications. The invention further provides methods of administering the film compositions by placing the composition into, for example, the oral cavity for a sufficient period of time to permit the film to disintegrate and release the active ingredient.


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