Method for the use of botanical extracts in the treatment of viral infections

1. A method for inhibiting a replication of a poxvirus by exposing the poxvirus to a liquid extract from a plant material selected from Sarracenia, Nepenthes, Melissa, Lavandula, Glycyrrhiza, Eleutherococcus, Hypericum, Darlingtonia, Heliamphora, Roridula, Drosera, Dionaea, Aldrovanda, Drosophyllum, Triphyophyllum, Catopsis, Brocchinia, Paepalanthus, Uricularia, Genlisea, Pinguicula, Ibicella, Byblis, Philcoxia, Stylidium and Cephalotus wherein the plant material is prepared by steps comprising:

obtaining fresh plant material less than about ten (10) days following harvest of the plant material;

washing and air drying the plant material;

combining the plant material with a liquid comprising ethanol and glycerol at a ratio of about one (1) gram of the plant material to about fifteen (15) milliliters of the liquid;

allowing the liquid to extract the plant material at room temperature in an amber glass jar for about two (2) to about sixty (60) days or by boiling for between about thirty (30) minutes to about four (4) hours to form the liquid extract; and

separating the liquid extract from the plant material.

2. The method of claim 1 wherein the poxvirus is selected from the group consisting of orthopoxvirus, parpoxvirus, avipoxvirus, capripoxvirus, leporipoxvirus, suipoxvirus, molluscipoxvinis molluscipox virus and yatapox virus.

3. The method of claim 1 , wherein the pox virus is selected from the group consisting of vaccinia virus, monkeypox virus, variola virus, and molluscum contagiosum virus.

4. The method of claim 1 , further comprising steps standardizing a biological activity of the liquid extract comprising:

growing a cell culture to a target cell density for a viral infection;

preparing a dilution of a viral stock to a known plaque forming unit (pfu) concentration;

preparing a serial dilution of the liquid extract to produce a plurality of liquid extract treatment concentrations;

combining the dilution of the viral stock with each of the plurality of liquid extract treatment concentrations;

adding each of the plurality of liquid extract treatment concentration/viral stock combinations to an aliquot of the cell culture to produce a plurality of infected cell cultures;

adding a fresh equivalent liquid extract treatment concentration to each of the plurality of infected cell cultures;

incubating each of the plurality of the infected cell culture/liquid extract combinations;

measuring a viral plaque formation by counting the number of viral plaques and reporting the viral plaque formation as a percentage of plaque formation, wherein the percentage of plaque formation is the observed number of plaques divided by an expected number of plaques based on the viral concentration of the viral stock aliquot; and

determining the biological activity of the liquid extract from the percentage of viral plaque formation.

5. The method of claim 4 , wherein the liquid extract comprises about 50% of an extract of Sarracenia purpurea having biological activity of about fifty (50) viral inhibitory units per milliliter and about 12% of an extract of Melissa officinalis having a biological activity of about eighty (80) viral inhibitory units per milliliter.