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Currently there is a crisis in the supply of antivenom for treatment of snake bite in sub-Saharan Africa. Commercial pressures have resulted in the reduction or even cessation of production of antivenom by European manufacturers while continued production of antivenom in Africa has been threatened by the privatisation of the only remaining company based in Africa. As a consequence, there has been...
Separation of previously uncharacterised Echis ocellatus venom by phenyl-Superose FPLC (Fast Liquid Protein Chromatography) yielded eight protein fractions. Three of these displayed high proteolytic activity when assayed by in vivo and in vitro assays (including enzyme linked immunosorbant assay), and were further separated using Superdex 75 and Mono-Q FPLC. This resulted in the purification of a...
The preclinical evaluation of the efficacy of new antivenoms (ED50) in animals is required by international regulatory authorities. In vitro testing alone does not provide the end point of lethality of a living system which is essential for an antivenom to prevent. Large numbers of mice are injected with venom/antivenom mixtures and the number of surviving mice is statistically analysed to give an...
One of the tests used routinely for the preclinical assessment of antivenom efficacy is the WHO-approved rodent intradermal skin test for assessing neutralization of venom-induced haemorrhagic activity. This is a useful test as in many viperid venoms haemorrhage is considered to be the principal lethal (pathogenic) venom effect in envenomed humans. The main problems with such an assay are, first,...
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