Pharmaceutical composition comprising modified polyriboinosinic-

Drug – bio-affecting and body treating compositions – Immunoglobulin – antiserum – antibody – or antibody fragment,... – Reduced antigenicity – reduced ability to bind complement – or...

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424 85, 424180, 536 28, 536 29, A61K 3702, A61K 4502

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active

043883060

ABSTRACT:
A complex of polyriboinosinic-polyribocytidylic acid (poly I:C) with poly-L-lysine hydrobromide ([lysine.HBr].sub.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, containing 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.

REFERENCES:
patent: 3679654 (1972-07-01), Maes
patent: 3725545 (1973-04-01), Maes
patent: 3952097 (1976-04-01), Levy
patent: 4024222 (1977-05-01), Ts'o et al.
patent: 4130641 (1978-12-01), Ts'o et al.
Carrol, Biochemistry, vol. 11, pp. 426-433, (1972).
Haynes, Biochemistry, vol. 9. pp. 4410-4416, (1970).
Catalona, Pro. Soc. Exp. Bio. & Med., vol. 140, pp. 66-71, (1972).
Wacker, Archiv. fur die gesamte Virusforschung, vol. 36, pp. 71-79, (1972).

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