Method for combining power-frequency electromagnetic field generating device with platinum-based drugs
A generation device and platinum-based drug technology, applied in the field of biotechnology and medical treatment, can solve the problems of lack of unified and complete understanding, complex biophysical mechanism of action, etc., and achieve uniform magnetic field strength, convenient implementation, and reduced dose effects.
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Embodiment 1
[0022] Example 1, the combination method of the magnetic field generating device of the present invention and platinum-based drugs
[0023] This method is realized through the following steps: build a power frequency electromagnetic field generating device, use a power frequency 50 / 60Hz power supply, and continuously change the voltage through a DC and AC autotransformer, thereby generating superimposed static (from DC) and alternating currents inside the irradiation part. (from AC) electromagnetic field, the average strength of the loaded magnetic field is 5.5 millitesla (mT), and the total irradiation time for the irradiated object on the irradiated part is 60-120 minutes per day; For the irradiated object, platinum drugs such as cisplatin, carboplatin, oxaliplatin and other platinum drugs are selected. Administered 3 times a week, this is the lower dose selected within the effective dose range of cisplatin.
[0024] see figure 1, the power frequency electromagnetic field ...
Embodiment 2
[0030] Example 2, the present invention acts on the cultured Wilms tumor cells G401, the control group, the irradiation group, the cisplatin group, and the combination group are treated separately, and each treatment condition has 3 duplicate wells, and the cells treated the day before are collected every day , count with a living cell counter, calculate the number of cells according to the readings, and make a cell proliferation curve and an electromagnetic field inhibition curve for cells.
[0031] The specific implementation process is as follows:
[0032] Cell line and culture method: Wilms tumor cell G401, which is an adherent cell, was cultured in McCoy medium containing 10% fetal bovine serum in an incubator at 37°C, containing 5% carbon dioxide and saturated water vapor.
[0033] Main equipment: power frequency electromagnetic field generator, cell incubator, living cell counter.
[0034] Cell viability test: Wilms tumor cell G401 was seeded on a 6-well plate at a den...
Embodiment 3
[0037] Example 3, the present invention acts on the cultured neuroblastoma cell CHLA255, the control group, the irradiation group, the cisplatin group, and the combination group are treated separately, and each treatment condition has 3 duplicate wells, and the cells treated the day before are collected every day , count with a living cell counter, calculate the number of cells according to the readings, and make a cell proliferation curve and an electromagnetic field inhibition curve for cells.
[0038] The specific implementation process is as follows:
[0039] Cell line and culture method: Neuroblastoma cell CHLA255, which is an adherent cell, was cultured in McCoy medium containing 10% fetal bovine serum in an incubator at 37°C, containing 5% carbon dioxide and saturated water vapor.
[0040] Main equipment: power frequency electromagnetic field generator, cell incubator, living cell counter.
[0041] Cell viability experiment: Neuroblastoma cells CHLA255 were seeded in 6...
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