Abstract
Quantitative haemadsorption proved to be a fast and reliable method in antiviral screening, using the haemagglutinating viruses of influenza A2 Japan, influenza A Swine (var), and parainfluenza Sendai. In the case of influenza B Johannesburg the method proved less reproducible. Evaluation of this method for these viruses, using monolayers of chick embryo fibroblasts and calf testicle cells is presented. The haemadsorption development paralleled the formation of haemagglutinin. The relation between dose and effect of 1-adamantanamine hydrochloride when used against the multiplication of influenza virus A Swine (var) is revealed by this method.
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