Slow release agent containing hormone kind anti cancer medicine
A technology of anticancer drugs and hormones, applied in the field of medicine, can solve problems such as treatment failure and increased tolerance
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Embodiment 1
[0094] Put 70 mg of polyglycolic acid and glycolic acid copolymer (PLGA, 65:35) with a peak molecular weight of 20,000-40,000 into a container, add 100 ml of dichloromethane, dissolve and mix well, then add 10 mg of colchicine and 20 mg of other Moxifen, shake again and dry in vacuo to remove organic solvents. The dried solid composition is shaped immediately, subpackaged and sterilized by radiation to prepare an anticancer implant containing 10% colchicine and 20% tamoxifen. The drug release time of the anticancer implant in physiological saline in vitro is 15-20 days, and the drug release time of subcutaneous implantation in mice is 25-40 days.
Embodiment 2
[0096] The method steps of being processed into anticancer implants are the same as in Example 1, but the difference is that the anticancer active ingredients contained in the anticancer implants are:
[0097] 5-30% triptorelin, goserelin, leuprolide, anastrozole, edoxifene, milprexifen, tamoxifen, comoxifen, raloxifene, steroid Antiestrogens, anticancer stenols, 4-hydroxytamoxifen, flutamide, aminoglutethimide, piglutamide, megestrol, medroxyprogesterone, clomiphene, toremifene , letrozole or exemestane with 5-30% of cytochalasin, mitocloramine, mitoladone, mitoguanidine hydrazone, mitonaphthylamine, mitoxazine, mitokine, Tosper, Mitotane, Mitonamamine, Mitozolomide, Mitoransone, Colchicine Salicylate, Colchicine, Colcemid, Cytochalasin, Naphthol, Alpha-Naphthalene Combinations of phenol, beta-naphthol, alpha-naphthol phosphate, alcodazole, procodazole, arsenic, giraladazole, or nocodazole.
Embodiment 3
[0099] Put 70 mg of polylactic acid (PLGA, 50:50) with a peak molecular weight of 15,000-25,000 into a container, add 100 ml of dichloromethane, dissolve and mix well, add 20 mg of anastrozole and 10 mg of Xylomustine, and re-shake Dry in vacuo to remove the organic solvent. The dried solid composition is shaped immediately, subpackaged and then sterilized by radiation to obtain an anticancer implant containing 20% anastrozole and 10% sapromustine. The drug release time of the anticancer implant in physiological saline in vitro is 15-25 days, and the drug release time of the implant subcutaneously placed in mice is 25-45 days.
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