abstract |
A method for producing injectable quality pharmaceutical formulations of blood products, comprising the fractionation steps of the starting material in a two-phase aqueous polymer-salt system in the presence of phenol, purification of the upper phase of the system, by precipitation with Caprylic acid and purification of the lower phase by thermocoagulation, increased purity of the products in both phases by chromatography, removal of viral particles by nanofiltration of both preparations, and the formulation, stabilization and packaging of the products thus obtained. |