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filingDate 1980-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90e002af93d40263cccbc5ad2bd19354
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publicationDate 1983-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1156145-A
titleOfInvention Pharmaceutical composition comprising modified polyriboinosinic-polyribocytidylic acid, for induction of interferon in primates
abstract 16336IA TITLE OF THE INVENTION Pharmaceutical Composition Comprising Modified Polyriboinosinic-Polyribocytidylic Acid, for Induction of Interferon in Primates. ABSTRACT OF THE INVENTION A complex of polyriboinosinic-polyribocytidylic acid (poly I:C) with poly-L-lysine hydrobromide ([lysine.HBr]n) having a defined molecular weight is prepared which is about 5-15 times as resistant to hydrolysis by pancreatic ribonuclease as the parent poly I:C. A pharmaceutical solution, con-taining a relatively high concentration of the complex, prepared as described, induces significant antiviral levels of serum interferon in monkeys under conditions in which poly I:C itself induces little or no interferon. An important feature of this invention is that the product is a soluble material requiring no special solubilizing agent, thereby facilitating the preparation of solutions having the desired concentration. The product will hereinafter be designated as poly I:C/poly-L-lysine.
priorityDate 1979-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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