Flavin N-oxides: new anti-cancer agents and pathogen eradication agents
View Patent ↗Compounds comprising flavin N-oxides for treatments of solid tumors, non-solid tumor masses, leukemias, and non-small cell lung cancers and for eradicating contaminants in blood products. Methods of treating patients having solid type cancers comprising administering a therapeutically effective amount of a flavin N-oxide to a subject in need of treatment and exposing the flavin N-oxide to an activator such that activation of the flavin N-oxide results in damage to the DNA in the cancer cells without substantial damage to the DNA of normal cells are also provided. Methods of using a flavin N-oxide as part of a combination therapy with chemotherapy, radiation therapy, or both are also provided. Methods of reducing pathogenic bacterial or viral contamination in a composition comprising a) mixing the composition with an efficacious amount of a flavin N-oxide and b) exposing the mixture of the composition and the flavin N-oxide to an activator for a period of time sufficient to activate the flavin N-oxide such that the flavin N-oxide reduces the contamination in the composition are also provided. Preferably, the composition is a blood product selected from plasma, platelets, and red blood cells and the activator is an enzyme.
1. A method of treating a subject having a solid tumor, a non-solid tumor mass, leukemia, or non-small cell lung cancer comprising:
a. administering a therapeutically effective amount of a flavin N-oxide to the subject; and
b. exposing the flavin N-oxide to an activator, such that activation of the flavin N-oxide results in damage to the DNA in the cancer cells without substantial damage to the DNA in normal cells.
2. The method of claim 1 wherein the flavin N-oxide is of formula I:
wherein
X 1 is selected from H, monosaccharides, substitited monosaccharides, mono, di, and tri-ethylene glycol, alcohol, and alkyl ammonium ion; and
X 2 , X 3 , and X 4 can be the same or different and are selected from H, monosaccharides, substitited monosaccharides, glycol, alcohol, lower alkyl, and alkylene groups;
wherein X 2 , X 3 , and X 4 can be substituted with monosaccharides, substitited monosaccharides, mono, di, and tri- ethylene glycol, alcohol, alkyl ammoniuni ion, and combinations thereof.
3. The method of claim 2 wherein the flavin N-oxide is riboflavin N-oxide.
4. The method of claim 1 wherein the activator comprises a reducing enzyme.
5. The method of claim 4 wherein the reducing enzyme is present in the cancer cells.
6. The method of claim 1 wherein the activator is electromagnetic radiation of sufficient wavelength and intensity to activate the flavin N-oxide.
7. The method of claim 6 wherein the electromagnetic radiation is X-ray radiation.
8. The method of claim 1 wherein the flavin N-oxide preferentially kills cancer cells rather than normal cells in a ratio of at least 5:1.
9. The method of claim 1 wherein the flavin N-oxide preferentially kills cancer cells rather than normal cells in a ratio of at least 10:1.
10. The method of claim 1 wherein the flavin N-oxide is used as part of a combination therapy.
11. The method of claim 10 wherein the combination therapy comprises radiation therapy.
12. The method of claim 10 wherein the combination therapy comprises chemotherapy.
13. The method of claim 10 wherein the combination therapy comprises chemotherapy and radiation therapy.