http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2621641-C

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_114e4423ec77cbc8dab9d0a98909704e
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S977-906
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-5161
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filingDate 2005-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ebd13c4daaf47a15f3ccaa9d657c741
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_618bbca54f57794eadb6bacd61c4eaf3
publicationDate 2014-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2621641-C
titleOfInvention Ph sensitive nanoparticle formulation for oral delivery of proteins/peptides
abstract The present invention provides a pH sensitive nanoparticulate delivery system for the administration of peptide hormones and drugs. In particular it provides a pH sensitive nanoparticulate for oral insulin administration. The nanoparticles developed by this process are fatty acid nanoparticles and a polymer is used as a stabilizer and also to incorporate pH sensitivity so that these particles shrink in the gastric acidic pH thereby protecting the incorporated insulin. These particles being also hydrophobic in nature and by virtue of their small size get absorbed through the intestinal cell wall and Peyer's patches. These nanoparticles are novel and unique in the sense that polymer content is only 0.03-0.06g/g product and the polymer is hydrophilic in nature.
priorityDate 2005-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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