METHOD FOR TARGETTING GROWTH AND DEATH OF NEOPLASTIC CELLS BY BURSTS OF ENERGIES FROM CELLULAR ENERGY EMISSIONS

摘要

The embodiments herein disclose a non-invasive method of using bursts of energies/electromagnetic field energies from cells to reduce or arrest the growth rate, proliferation of cancer cells/neoplastic cells. The energy from cells induces apoptosis in cancer cells, without harming normal cells beyond their physiologic threshold of survival are provided. The embodiments herein disclose a method for treatment of cancer/neoplastic cell in human or animals within the context of cancer therapeutics. A cell culture plate is incubated. This plate serves as the source of bursts energies/electromagnetic field energies. Further with a device the bursts of energies are targeted to another plate having cells for one week. After one week the microscopic examination is done. The rate of growth of cell is six to seven pulsatile cells per square centimetre. The energy from cells kills cancer cells, induce apoptosis, stimulate growth phase in cell culture and enables harmonics therapy.

主权项

1. A method for stimulating a cell culture for growth with bursts of energies/cellular signals of cells, the method comprises the steps of:
culturing CD34 cells in three different culture plates comprising a culture medium by following a standard culture protocol; labelling a first culture plate as a control plate, and wherein the control plate comprises the CD 34 cells in a culture medium, and wherein the first culture plate is incubated at 37° C. for one week, and wherein the first culture plate is not exposed to any bursts of energies/cellular signals of cells; subjecting a second culture plate comprising CD 34 cells in a culture medium to a red light, and wherein the CD34 cells are stimulated by the red light constantly for one week, and wherein the second culture plate is incubated at 37° C. for one week; subjecting a third culture plate comprising CD 34 cells in a culture medium to a plurality of bursts of energies/cellular signals of the CD34 cells in the second culture plate with a device, and wherein the plurality of bursts of energies/cellular signals of the CD34 cells is detected and amplified by a photo multiplier, and wherein the third culture plate is incubated at 37° C. for one week; and wherein the three culture plates comprising CD 34 cells are analyzed microscopically after one week.