http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2253980-C
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4fa4c37b4aacb317ee027a1a729de4ff |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-7007 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-0063 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-52 |
| filingDate | 1997-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2004-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_941f00712f427fe45eaa2401f6da7f78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a52ee6ffb6042fa28ec4260e0324175a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b82c61d8e2480b7ea595f43603b38d9b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0160cc4f161b1f74917c9e87b0b372e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_690b4bb5226f50c53ecd448aa8fe8934 |
| publicationDate | 2004-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-2253980-C |
| titleOfInvention | Locally administrable, biodegradable and sustained-release pharmaceutical composition for periodontitis and process for preparation thereof |
| abstract | This invention relates to locally administrable, biodegradable and sustained-release pharmaceutical composition for periodontitis and process for preparation thereof, which can show continuous drug effect for a long time by controlling the release time and by making the drug remain in the periodontal pocket for a prolonged time. The composition is prepared by i) making a microsphere containing the physiologically active substance, ii) making the mixture of the microspheres and water-soluble polymer such as polysaccharides, iii) making the mixture into the form of film or strip or/and iv) coating the film or strip with a ration aqueous solution such as calcium and barium. The present pharmaceutical composition can be easily administered using forceps, has minimized side effects and maximizes the effect by releasing the active substance at the minimum dose, and makes the patients feel comfortable. |
| priorityDate | 1996-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 93.