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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61M1-3687
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-107
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61M1-36
filingDate 1978-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ceb4a87dfabfc28598813c98c99fb2e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c36dfd267b8015f27c7a95b79a67340a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_884e3b5a09a1fcfcd8635cf0cca4fb63
publicationDate 1980-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4183918-A
titleOfInvention Detoxifying-medicinal emulsions
abstract This invention relates to the use of liquid membrane technology in preparing medicinals. The medicinals prepared by this invention may be ingested and may be utilized as traps for toxins present in the GI (gastrointestinal) tract, or as slow-release compositions of drugs, or as reactors. In the trap embodiment, the liquid membrane encapsulated medicinal is an emulsion comprising an exterior phase which is immiscible with the liquids present in the GI tract and permeable to the toxins therein, and an interior phase which is immiscible with the exterior phase and comprises a reagent capable of converting said toxin into a nonpermeable form. In addition, hydrophilic adsorbents, such as a hydrophilic carbon or a silica gel, may be encapsulated in the emulsions of the instant invention. When the compositions of the instant invention are utilized as slow-release drugs, the interior phase of the emulsion will comprise a drug which is slightly soluble in the exterior phase of the emulsion whereby said drug permeates through said exterior phase of the emulsion over a period of time into the GI tract. The third method for utilizing the compositions of the instant invention comprises encapsulating a catalyst for a reaction which is desired to be carried out in the GI tract. In this embodiment the reactants present in the GI tract permeate through the exterior phase of the emulsion into an interior phase wherein said catalyst, for example, an enzyme, converts the permeated reactants to reaction products. The reaction products then may permeate through the exterior phase back into the GI tract. In all cases, the liquid membrane encapsulated medicinals may be administered by either oral ingestion or injection anywhere else into the GI tract.
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