Preparation method of anti-tumor microbubbles carrying chemotherapeutic drugs, medicament and application
A chemotherapy drug, anti-tumor technology, applied in the field of anti-tumor
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[0035] The invention relates to a preparation method, medicament and application of anti-tumor microbubbles carrying chemotherapeutic drugs. The anti-tumor microbubbles are produced by treating tumor cells with radiation; the chemotherapeutic drugs are common clinical chemotherapeutic drugs. The anti-tumor microvesicles carrying chemotherapeutic drugs have broad-spectrum anti-tumor activity and can effectively kill tumor cells of autologous origin and non-autologous origin. It can effectively treat tumors that are not sensitive to chemotherapy or tumors that cannot be directly treated by radiotherapy, either locally or intravenously. Its anti-tumor principle mainly involves the combined tumor killing effect of a large amount of reactive oxygen species carried by microvesicles and chemotherapy drugs, as well as the regulation of the tumor immune microenvironment, such as promoting the reprogramming of macrophages. The anti-tumor microvesicles carrying chemotherapy drugs are com...
Embodiment 1
[0056] Embodiment 1, constructing and quantifying the microvesicle protein concentration after radiotherapy, and quantifying the dose of chemotherapeutic drugs carried by high performance liquid chromatography, and the preservation method of microbubbles carrying chemotherapeutic drugs after radiotherapy.
[0057] Cultivate tumor cells in a 10mm×10mm culture dish with 10% FBS (fetal bovine serum) medium. When the number of cells in the culture dish reaches about 5×106, perform radiotherapy at a dose of 20GY. On the first day after radiotherapy Change the medium, add 20ml medium containing 10% FBS and a certain concentration of chemotherapeutic drugs, collect all the liquid in the culture dish on the third day, and use gradient centrifugation to extract microvesicles after radiotherapy. Take the cell culture medium after radiotherapy at 1000g and centrifuge for 10min, then take the supernatant, then centrifuge the supernatant at 14000g for 2min to remove debris, discard the prec...
Embodiment 2
[0058] Example 2, the killing effect of microbubbles carrying chemotherapeutic drugs on tumor cells after radiotherapy.
[0059] Prepare 100 μl of cell suspension in a 96-well plate with a cell density of 5×104 cells / ml. The 96-well plate was pre-incubated for 24 hours in an incubator (37° C., 5% CO 2 ). Add different amounts of microbubbles (0.04, 0.08, 0.12, 0.16mg / ml) carrying chemotherapeutic drugs produced by radiotherapy to the culture plate. The plates were incubated in the incubator for 48 hours. 10 μl of CCK8 (Cell Counting Kit-8) solution was added to each well, and the culture plate was incubated in an incubator for 2 hours, and the absorbance at 450 nm was measured with a microplate reader. The absorbance value reflects the activity of the cells. Such as image 3 As shown, as the number of anti-tumor microbubbles carrying chemotherapy drugs increases after radiotherapy, the killing ability of the microbubbles on tumor cells is gradually enhanced, and the killin...
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