ANTI-AIDS COCKTAIL CONSISTING OF AN ANTI-TUMORAL COMPOUND, A P-GLYCOPROTEIN INHIBITOR, AND AN ANTI-VIRAL AGENT

Abstract

The invention relates to a cocktail against Aids, consisting of a commercially available anti-tumoral drug (1), such as doxorubicin, idarubicin, etoposide, chlorambucil, cisplatin, melphalan or bortezomib, a P-glycoprotein inhibitor (2), such as tariquidar, cetoconazol, verapamil, amiodarone or quinidine, and a commercially available antiviral agent of the viricidal type (3) which acts directly on the virus, such as N,N-dichloro-2,2-dimethyltaurine (NVC-422) or the HIVcide nanoviricide, and designed to combat and completely eliminate the Aids virus from the organism.

Claims

1. An anti-Aids cocktail comprising an anti-tumoral compound, a p-glycoprotein inhibitor and an anti-viral agent, characterized in that it is a cocktail comprising the combination of an anti-tumoral medicament, an inhibitor of glycoprotein P, and an antiviral agent of the type viricide, all known commercially and administered M their recommended doses.

2. Cocktail according to claim 1, characterized in that it eliminates completely the HIV virus in the organism by the destroying action of the lymphocytes TCD4+ (the hiding-place of the HIV virus) by the anti-tumoral compound and by the inhibitor of glycoprotein P, exposing the virus later to the direct action of the viricide agent, thereby eliminating completely all the vira in the organism.

3. Cocktail according to claim 1, characterized in that it is a cocktail capable of eliminating completely the HIV virus in the organism by the synergistic effect of an anti-tumoral pharmaceutical of commercial use (1), such as doxorubicin or idarubicin, etoposide, chlorambucil, cisplatin, melflam, or bortezomib, or cyclosporine, and an inhibitor of P-glycoprotein (2), such as tariquidar, or cetoconazol, verapamil, miodaron, or quinidine, and an antiviral agent of the viricide type (3), which acts directly on the virus, such as N,N-dichloro-2,2-dimethyltaurin (NVC-422) or Nanoviricide (HIVCide), whereby the anti-tumoral and the inhibitor of glycoprotein P will destroy the hiding-place of the HIV virus in the TCD4+ lymphocytes, exposing the virus to the direct action by one of the antiviral compounds of the viricide type as mentioned above.

4. Cocktail according to claim 2, characterized in that it is a cocktail capable of eliminating completely the HIV virus in the organism by the synergistic effect of an anti-tumoral pharmaceutical of commercial use (1), such as doxorubicin, or idarubicin, etoptside, chlorambucil, cisplatin, metflam, or bortezomib, or cyclosporine and a inhibitor of P-glycoprotein (2), such as tariquidar, or cetoconazol, verapamil, miodaron, or quinidine, and an antiviral agent of the viricide type (3), which acts directly on the virus, such as N,N-dichloro-2,2-dimethyltaurin (NVC-422) or Nanoviricide (HIVCide), whereby the anti-tumoral and the inhibitor of glycoprotein P will destroy the hiding-place of the HIV virus in the TCD4+ lymphocytes, exposing the virus to the direct action by one of the antiviral compounds the viricide type as mentioned above.

Description

[0005] Referring now to the attached FIG. 1, this shows merely one composition possibility according to the inventive anti-Aids cocktail, formed by the combination of the antiviral agent N,N-dichloro-2,2-dimethyltaurin, with the anti-tumoral agent doxorubicin and with the inhibitor of the P-glycoprotein in this case tariquidar.

[0006] In accordance with the attached figure, the cocktail according to the present invention is an association of a commercial anti-tumoral medicament, such as doxorubicin (1), whose function is to destroy the hiding-place of the vira (i.e., the lymphocytes) by lowering the count of lymphocytes to zero in the blood by acting as an immunosuppressor, an inhibitor of P-glycoprotein, such as tariquidar (2), whose purpose is to maximize the preceding anti-tumoral compound in the lymphocytes, and an anti-virus of the viricide type, such as N,N-dichloro-2,2-dimethyltaurin (NVC-422) (3), which acts directly on the virus, whose purpose is to eliminate completely the Aids virus in the organism. The viricide agent NVC-422 oxidizes several amino-acids of the virus containing sulphur. The oxidation of these amino-acids results in alterations in the conformation of proteins and the morphology of the virus particle, resulting in a rapid loss of viral stability, deactivating them forever. In this way, the present anti-Aids cocktail will primarily lower to zero the number of lymphocytes in the blood of the infected individual, in view of the fact that the anti-tumoral agents above have a recognized immunosuppressive activity. In this way, the HIV virus is exposed in the blood plasma so that the anti-viral agent can act on them, deactivating them forever.

[0007] The concentration of the active agents (together) may vary considerably, but preferably is within the range 20 to 200 μg/ml of the commercial product, already including the other components, such as a vehicle.

[0008] Referring to said vehicles, these may be present in the form of diluents, as is well known in the state of the art. If diluents, carriers and/or other conventional additives are used, such as stabilizers, humidifying agents, emulsifiers, flavouring agents, buffers and similar, at least 1 to 80% by weight, preferably 1 to 25% by weight, and still more preferred, 2 to 15% by weight of the cocktail according to the invention should be composed of the three ingredients.