Anti solid tumor medicine composition
A tumor drug and composition technology, applied in the field of medicine, can solve the problem of local formation of effective drug concentration in difficult tumors, and achieve the effect of strengthening the anti-cancer effect
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Embodiment 1
[0092] Put 90 mg of polylactic acid (PLA) with a molecular weight of 10000 into a container, add 100 ml of dichloromethane, dissolve and mix well, add 10 mg of methoxyamine (MX), shake again and vacuum dry to remove organic solvents. The dried solid composition is immediately shaped, and then irradiated to sterilize it after packaging to obtain an anti-cancer complex containing 10% by weight of MX. The drug release time of the anti-solid tumor drug composition in vitro in physiological saline is 15-20 days, and the drug release time under the skin of mice is about 30-40 days.
Embodiment 2
[0094] The method steps for processing into an anti-solid tumor pharmaceutical composition are the same as in Example 1, but the active ingredients contained are:
[0095] Ethylene Vinyl Acetate Copolymer (EVAc) 85 mg
[0096] Dichloromethane 100 ml
[0097] DNA repair enzyme inhibitor (MX) 15 mg
[0098] According to the above method, it was made into a compound containing 15% MX by weight.
Embodiment 3
[0100] The method steps for processing into an anti-solid tumor pharmaceutical composition are the same as in Example 1, but the active ingredients contained are:
[0101] PLGA (copolymer of lactic acid and glycolic acid) with a molecular weight of 20,000 75 mg
[0102] Dichloromethane 100 ml
[0103] Hydroxylamine (HX) 25 mg
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