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filingDate 1999-01-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2002-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002524494-A
titleOfInvention Orally administered controlled drug delivery system providing temporal and spatial control
abstract A pharmaceutical composition in the form of a tablet or capsule provides a combination of temporary and controlled delivery of a drug to a patient for effective therapeutic results. The pharmaceutical composition includes a drug, a gas generating component, a swelling agent, a viscosity-imparting agent, and a gel-forming polymer. Swelling agents belong to the class of compounds known as superdisintegrants (eg, cross-linked polyvinyl pyrrolidone or cross-linked sodium carboxymethyl cellulose). Initially, the viscosity-imparting agent, and then the gel-forming polymer, forms a hydrated gel matrix that traps the gas, thereby suspending the tablet or capsule, so that it becomes the upper surface of the stomach or small intestine ( Spatial control) is stagnated. At the same time, the hydrated gel matrix created a meandering diffusion path for the drug, thereby resulting in sustained release (temporary control) of the drug. A preferred once-daily ciprofloxacin formulation is 69.9% ciprofloxacin base, 0.34% sodium alginate, 1.03% xanthan gum, 13.7% sodium bicarbonate, 12.1% cross-linked polyvinyl. Including pyrrolidone, and optionally other pharmaceutical excipients, the formulation is in the form of coated or uncoated tablets or capsules.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017518349-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009502897-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004513975-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009501777-A
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type http://data.epo.org/linked-data/def/patent/Publication

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