Method for expanding tumor ablation range
A kind of technology with a wide range of tumors, which is applied in the direction of anti-tumor drugs, pharmaceutical formulas, parts of surgical instruments, etc., can solve the problems of cell failure and apoptosis, and achieve the effect of expanding the ablation area and improving the anti-tumor effect
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Embodiment 1
[0037] (1) Human breast cancer cells EFM-192A were cultured in cell culture medium (Dulbecco modified Egle medium, DMEM) containing 10% fetal bovine serum and 1% penicillin / streptomycin (PS), and the incubator environment was CO 2 The concentration is 5% and the temperature is 37°C. Cells were passed through 0.25% GIBCO before use ® trypsin-EDTA solution was harvested and passed through a cell counter (Countstar ® BioTech, Shanghai Ruiyu Biotech Co., Ltd., Shanghai, China) ensure that the cell concentration in the cell suspension is 2×10 6 cells / ml (overall survival rate >97%);
[0038] (2) Add human breast cancer cells EFM-192A to DMEM and place them in a cell culture dish with a cell volume of 2×10 7 , adding the conductive nanoparticles / drug-targeting composite material so that the concentration of the conductive nanoparticles / drug-targeting composite material in DMEM is 0.5 mg / mL;
[0039] (3) Implant two IRE needle-shaped electrodes in the cell culture dish, the needl...
Embodiment 2
[0041] (1) Human breast cancer cell MCF-7 was cultured in cell culture medium (Dulbecco modified Egle medium, DMEM) containing 10% fetal bovine serum and 1% penicillin / streptomycin (PS), and the incubator environment was CO 2 The concentration is 5% and the temperature is 37°C. Cells were passed through 0.25% GIBCO before use ® trypsin-EDTA solution was harvested and passed through a cell counter (Countstar ®BioTech, Shanghai Ruiyu Biotech Co., Ltd., Shanghai, China) ensure that the cell concentration in the cell suspension is 2×10 6 cells / ml (overall survival rate >97%).
[0042] (2) Take human breast cancer cell MCF-7 and add it to DMEM and place it in a cell culture dish, the cell volume is 3×10 7 , adding conductive nanoparticles / drug-targeting composite material, so that the concentration of conductive nanoparticles / drug-targeting composite material in DMEM is 0.8 mg / mL;
[0043] (3) Six IRE needle electrodes are implanted in the target area of the tumor tissue in t...
Embodiment 3
[0045] (1) Human breast cancer cells MD-MB-231 were cultured in cell culture medium (Dulbecco modified Egle medium, DMEM) containing 10% fetal bovine serum and 1% penicillin / streptomycin (PS), and the incubator environment was CO 2 The concentration is 5% and the temperature is 37°C. Cells were passed through 0.25% GIBCO before use ® trypsin-EDTA solution was harvested and passed through a cell counter (Countstar ® BioTech, Shanghai Ruiyu Biotech Co., Ltd., Shanghai, China) ensure that the cell concentration in the cell suspension is 2×10 6 cells / ml (overall survival rate >97%).
[0046] (2) Human breast cancer cells MD-MB-231 were added to DMEM and placed in a cell culture dish with a cell volume of 5×10 5 , adding the conductive nanoparticles / drug-targeting composite material so that the concentration of the conductive nanoparticles / drug-targeting composite material in DMEM is 1 mg / mL;
[0047] (3) Implant 3 IRE needle electrodes in the tumor tissue target area in the c...
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