Method for inactivating non-enveloped viruses using a viricide-potentiating agent with a photoactivatible virucide
AssigneeHemasure, Inc.
InventorsCharles M. Zepp, Donald L. Heefner
Life of this patent
Estimating the term…
Loading patent…
AssigneeHemasure, Inc.
InventorsCharles M. Zepp, Donald L. Heefner
Estimating the term…
Method for inactivating non-enveloped viruses using a viricide-potentiating agent. In a preferred embodiment, the method may be used to inactivate non-enveloped viruses present within a sample of whole blood or a blood product and comprises (a) adding to the blood sample a photoactivatable viricide, such as a psoralen, hypericin, methylene blue, toluidine blue or the like, which, when activated, is effective in inactivating enveloped viruses; (b) adding to the blood sample a viricide-potentiating chemical agent that increases the sensitivity of non-enveloped viruses to the activated viricide; and (c) activating the photoactivatable viricide. Preferably, the viricide-potentiating chemical agent includes a first moiety which possesses an affinity for a component of the non-enveloped virus and a second moiety which includes a lipid tail, the first and second moieties being structurally interrelated so that, when the first moiety becomes associated with a component of the non-enveloped virus, the second moiety penetrates or at least partially surrounds the viral capsid of the non-enveloped virus. Examples of the chemical agent include cationic lipopolyamines, such as dioctadecylamidoglycylspermine.
A method for inactivating a non-enveloped virus, the non-enveloped virus having a viral capsid, said method comprising the steps of:
A method of increasing the susceptibility of a non-enveloped virus to a photoactivatable viricide, the non-enveloped virus having a viral capsid, said method comprising the step of administering to the non-enveloped virus a viricide-potentiating chemical agent in a concentration that increases the efficacy of the photoactivatable viricide against the non-enveloped virus, said viricide-potentiating chemical agent being selected from the group consisting of cationic lipopolyamines, 2-methoxy-6-chloro-9-octadecylaminoacridine and the following compound;
A method for inactivating a non-enveloped virus in a sample, the non-enveloped virus having a viral capsid, the sample consisting essentially of at least one of blood plasma, red blood cells and platelets, said method comprising the steps of:
A method for inactivating a non-enveloped virus, the non-enveloped virus having a viral capsid, said method comprising the steps of:
Dependencies are inferred from the claim text.