Pharmaceutical composition and uses thereof
A composition and drug technology, applied in the field of preparing exosomes tumor vaccines, pharmaceutical compositions containing procaine and MS-275, can solve the problems of unsatisfactory, negative, rare, etc., and prevent the occurrence of tumors , Wide antigen spectrum, less toxic and side effects
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Embodiment 1
[0038] Example 1 Cell Culture
[0039] Experimental materials: H22 cell line, 10% fetal bovine serum, penicillin and streptomycin mixture (Beijing Tigemei Company).
[0040] Experimental method: culture H22 cell line in the culture medium containing 10% fetal bovine serum, penicillin 100IU / mL, streptomycin 100×μg / mL, at 37°C and 5% CO 2 Culture in the incubator, when the cells grow to the logarithmic phase, press 3×10 6 / 100ml inoculation.
Embodiment 2
[0041] Embodiment 2 drug treatment
[0042] Experimental materials: procaine, MS-275 (both purchased from sigma company).
[0043] Experimental grouping: the volume of cell culture medium is strictly consistent in each group, blank control group, exosomes control group (no drug addition group), exosomes experimental group 1 (adding procaine), exosomes experimental group 2 (adding drug MS-275) , exosomes experimental group 3 (combined administration of procaine and MS-275).
[0044] Experimental method: in the control group, no drug was added after inoculation, and 150ml of the supernatant was collected as a control after 24 hours; -6 mol / L of procaine, respectively collected 150ml of culture supernatant 24h after dosing; dosing group 2, 24h after inoculation with a concentration of 1 × 10 -6 mol / L MS-275 treatment, respectively collected 150ml of culture supernatant 24h after dosing; dosing group 3, 24h after inoculation with 1 × 10 -6 mol / L procaine and 1×10 -6 mol / L MS-2...
Embodiment 3
[0045] The separation and purification of embodiment 3 exosomes
[0046] Experimental equipment: HMAC-CP70G low temperature ultra-high speed centrifuge, 100KU MW CO Millipore Amicon high recovery rate high flow rate tangential flow ultrafiltration centrifuge tube (Millipore Company).
[0047] Experimental method: Centrifuge the collected cell culture supernatants of the experimental group and the control group at 300g for 10min to remove the cells, and take the supernatant; centrifuge at 1500g for 30min to remove the cell debris, collect the supernatant, and concentrate it through a 100kUMWCO Centriplus centrifugal ultrafiltration tube Ultrafiltration, centrifugation at 1500g for 30min to obtain 6ml of concentrated solution, transfer the separated and purified concentrated solution to a 1.5ml centrifuge tube, and ultracentrifuge at 100kg for 60min at 4°C with a horizontal rotation angle to obtain exosomes.
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