http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2005025839-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K33-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-522
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-522
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K33-14
filingDate 2004-07-26^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_285e99c98cdfe52420ff47b8bdd7bee5
publicationDate 2005-02-03^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2005025839-A1
titleOfInvention Formulation approach to enhance transporter-mediated drug uptake
abstract Transporters are membrane proteins that translocate solutes across biological membranes. Active agents such as drugs, prodrugs, nutrients, nutraceuticals, and other bioactive substances are substrates for transporters. Some transporters require sodium to be co-transported with solute, in order to transport solute. This invention relates to a pharmaceutical formulation approach to enhance uptake of active agent by increasing the uptake of active agent by a sodium-dependent transporter, where sodium is fabricated with or co-administered with active agent. One example is the formulation of a dosage form containing the prodrug acyclovir valychenodeoxycholate, which targets the human apical sodium-dependent bile acid transporter, and sodium chloride to enhance active agent uptake from the gastrointestinal tract.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3393469-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8470543-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10857152-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10953011-B2
priorityDate 2003-07-28^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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