Medicine for treating carbon ion radiotherapy-chemotherapy syndromes of esophageal cancer and preparation method thereof
A technology of carbon ions and syndromes, applied in biochemical equipment and methods, drug combinations, pharmaceutical formulations, etc., can solve problems such as difficulty in finding effective single-drug effective monomers, inability to treat esophageal cancer, and high incidence of complications, and achieve Improve the inhibition rate and lethality, good physical strength, and the effect of definite curative effect
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[0039]like figure 1 As shown, the preparation method of the medicine for the treatment of esophageal cancer carbon ion radiotherapy and chemotherapy syndrome provided by the embodiments of the present invention comprises the following steps:
[0040] S101. Weigh the recombinant human superoxide dismutase, Cistanche tuberosa, Myrobalan, Pulsatilla, Fritillaria, Licorice, Coptis Rhizoma, mannitol, trehalose and antioxidants in sequence according to the parts by mass.
[0041] S102, adding a small molecule water solvent into a glass reactor, sequentially adding recombinant human superoxide dismutase, mannitol, trehalose and antioxidants and stirring at a speed of 10-50r / mim to obtain a mixed solution A.
[0042] S103, using 75% ethanol to soak Cistanche tuberosa, repeat extraction twice at a solid-to-liquid ratio of 1:10, each time for 1 hour, and obtain and purify the Cistanche tuberose extract.
[0043] S104, using Pulsatilla Radix and Coptidis Rhizome to prepare the alcohol e...
Embodiment 1
[0064] Esophageal cancer cells Eca-109 and EC9706 were inoculated into 96-orifice plate with the quantity of 4000-6000 cells per well, after the cells adhered to the wall (24h), the medicine of the present invention was diluted into a certain gradient concentration, and each concentration was set at 5 Repeat hole. After 48 hours, use the MTT method to detect cell viability. Add 10 μl of MTT solution to each well and continue to incubate for 4 hours. Carefully suck out the liquid in the wells to avoid contact with crystals in the wells. Add 100 μl of DMSO to each well and shake on a constant speed shaker in the dark. . After the crystals are fully dissolved, read the OD value (wavelength 570nm, reference wavelength 630nm) on a microplate reader, and measure the absorbance A value.
[0065] The calculation formula of growth inhibition rate is: growth inhibition rate (%)=(1-OD)×100%. According to the inhibition rate of each concentration, the dose-response curve can be obtained...
Embodiment 2
[0067] Embodiment 2: Esophageal cancer cell invasion test ( image 3 )
[0068] Before the experiment, Matrigel was taken out from the -20°C refrigerator and placed in a 4°C refrigerator overnight. First, dilute Matrigel to 200ng / ml, add 1640 culture solution at 4°C, spread the diluted liquefied Matrigel on a Transwell polycarbonate membrane, and dry it in a 37°C thermostat for 6 hours to solidify to form a matrix Barrier glue. The prepared Transwell polycarbonate membrane was irradiated with light for 2 hours, and a small amount of sterilized serum-free 1640 medium was added to hydrate the Transwell polycarbonate membrane before use. The Eca-109 and EC9706 cells in the logarithmic phase were washed twice with PBS, digested routinely, centrifuged and the cell culture medium was discarded, the cells were gently rinsed with PBS buffer for 3 times, and the cells were resuspended in BSA-containing medium. in serum-free medium. Adjust the concentration of the cell suspension to...
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