Nanosecond pulsed electric fields cause melanomas to self-destruct
Methods for a new, drug-free therapy for treating solid skin tumors through the application of nanosecond pulsed electric fields (“nsPEFs”) are provided. In one embodiment of the invention, the cells are melanoma cells, and the applied nsPEFs penetrate into the interior of tumor cells and cause tumor cell nuclei to rapidly shrink and tumor blood flow to stop. This new technique provides a highly localized targeting of tumor cells with only minor effects on overlying skin.
1. A method for selectively initiating apoptosis in skin cells in a tissue comprising coating a skin tissue with a composition that reduces flashover during pulse field application; and applying at least 100 nsPEFs to said tissue, wherein each nsPEF has a pulse duration of at least about 10 nanoseconds and no more than about 1 microsecond and an electric field pulse strength of at least about 10 kV/cm and no more than about 350 kV/cm.
2. The method of claim 1 , whereby said method is carried out in situ.
3. The method of claim 1 , wherein each nsPEF has a pulse duration of at least about 300 nanoseconds and an electric field pulse strength of at least about 20 kV/cm and no more than about 125 kV/cm.
4. The method of claim 1 , wherein said method is repeated one or more times.
5. A method for inhibiting blood flow in a tissue comprising skin cells the method comprising:
coating a skin tissue with a composition that reduces flashover during pulse field application; and
applying at least 100 nsPEFs to said skin tissue, wherein each nsPEF has a pulse duration of at least about 10 nanoseconds and no more than about 1 microsecond and an electric field pulse strength of at least about 10 kV/cm and no more than about 350 kV/cm.
6. The method of claim 5 , whereby said method is carried out in situ.
7. The method of claim 5 , wherein each nsPEF has a pulse duration of at least about 300 nanoseconds and an electric field pulse strength of at least about 20 kV/cm and no more than about 40 kV/cm.
8. The method of claim 5 , wherein said method is repeated one or more times.
9. A method for inducing tumor regression in a tumor located in skin tissue comprising:
coating a skin tissue overlying the tumor with a composition that reduces flashover during pulse field application; and
applying at least 100 nsPEFs to said tumor, wherein each nsPEF has a pulse duration of at least about 10 nanoseconds and no more than about 1 microsecond and an electric field pulse strength of at least about 10 kV/cm and no more than about 350 kV/cm.
10. The method of claim 9 , whereby said method is carried out in situ.
11. The method of claim 9 , wherein each nsPEF has a pulse duration of at least about 300 nanoseconds and an electric field pulse strength of at least about 20 kV/cm and no more than about 40 kV/cm.
12. The method of claim 9 , wherein said method is repeated one or more times.
13. The method of claim 9 , wherein the method is repeated two to three weeks after initially applying the at least 100 nsPEFs.
14. A method for inducing tumor regression in a tumor, the method comprising:
coating a tissue overlying the tumor with a composition that reduces flashover during pulse field application; and
applying at least 100 nsPEFs to said tumor, wherein each nsPEF has a pulse duration of at least about 10 nanoseconds and no more than about 1 microsecond and an electric field pulse strength of at least about 10 kV/cm and no more than about 350 kV/cm.
15. The method of claim 14 , wherein the tissue is one or a combination of any of the following: fat, bone, skin, muscle, cartilage.
16. The method of claim 14 , wherein the at least 100 nsPEFs are applied through a catheter electrode.
17. The method of claim 14 , wherein the electric field pulse strength is between about 20 kV/cm and about 45 kV/cm.
18. The method of claim 14 , wherein each nsPEF has a pulse duration of at least about 300 nanoseconds.
19. The method of claim 14 , wherein the tumor comprises cancer cells.