Anti entity tumour medicinal composition
A technology of tumor drugs and compositions, which is applied in the field of drugs, and can solve the problems of limited and difficult local formation of effective drug concentrations in tumors, etc.
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Embodiment 1
[0087] Put 80 mg of polyglycolic acid and glycolic acid copolymer (PLGA) with a molecular weight of 10,000 into a container, add 100 ml of dichloromethane, dissolve and mix well, add 10 mg of vincristine and 10 mg of mitomycin C, and re-shake After homogenization, the organic solvent was removed by vacuum drying. The dried solid composition is shaped immediately, subpackaged and then sterilized by radiation to obtain an anti-solid tumor pharmaceutical composition containing 10% vincristine and 10% mitomycin C, both by weight percentage. The drug release time of the anti-solid tumor pharmaceutical composition in physiological saline in vitro is 15-20 days, and the drug release time in mouse subcutaneous is 30-40 days.
Embodiment 2
[0089] The method step of being processed into the anti-solid tumor pharmaceutical composition is the same as in Example 1, but the difference is that the contained anti-cancer active ingredients are:
[0090] (A) 1-50% of vinblastine, isovinblastine, vinblastine, vinblastine, vinblastine, vincristine, podiazine, vincristine sulfate, vinblastine, anhydrovinblastine tartrate , Epoxy Vinblastine Tartrate, Epoxy Vinblastine, Vinblastine Tartrate, Hainan Crude Torresine, Hainan Crude Torrellactone, Vinpocetine, Vinorelbine, Bitartrate, Vinorelbine Ditartrate, Vinorel Tartrate Bin, vinblast, vinblast, vinblastol, vinblast, vinblastine sulfate, vinblast, vinblastine, vinblast, changflunine, vinbendine, vinblastine, vinblastine, Vinblastol, vinblastine, oxymatrine, harringtonine, deoxyharringtonine, homoharringtonine, pearl cyst shellin, monocrotaline, maytansin, erythrin, camel Total Alkaloids, Cardiolide, Maidensine, Rubescensine A, Zhangzhou Narcisine, Pronarcisine Hydrochloride,...
Embodiment 3
[0094]Put 80 mg of polyglycolic acid and glycolic acid copolymer (PLGA) with a molecular weight of 20,000 into a container, add 100 ml of dichloromethane, dissolve and mix well, add 10 mg of vinblastine and 10 mg of doxorubicin, and re-shake Dry in vacuo to remove the organic solvent. The dried solid composition is shaped immediately, subpackaged and sterilized by radiation to obtain an anti-solid tumor pharmaceutical composition containing 10% vinblastine and 10% doxorubicin. All are percentages by weight. The drug release time of the anti-solid tumor pharmaceutical composition in physiological saline in vitro is 15-20 days, and the drug release time in mouse subcutaneous is 30-40 days.
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