Pharmaceutical composition for solid tumour
A technology of tumor drugs and compositions, which is applied in the field of medicine, can solve the problems of local formation of effective drug concentrations and limitations in difficult tumors, and achieve the effects of prolonging local drug concentrations, reducing systemic toxic reactions, and enhancing anticancer effects
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Embodiment 1
[0053] Put 90 mg of polylactic acid (PLGA) with a molecular weight of 10,000 into a container, add 100 ml of dichloromethane, dissolve and mix, add 10 mg of oxaliplatin, re-shake, and then vacuum-dry 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% by weight of oxaliplatin. 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
[0054] Embodiment 2. As described in embodiment 1, the difference is that the contained anticancer active ingredients are:
[0055] 0.1-30% Heptaplatin, Denaplatin, Enloplatin, Cycloplatin, Cispiroplatin, Dexomaplatin, Isoproplatin, Lobaplatin, Miplatin, Nedaplatin, Omaplatin, Siplatin, Spiroplatin or zeniplatin. All are percentages by weight.
Embodiment 3
[0057] Put 80mg of polyphenylpropane (p-CPP: 20:80 of sebacic acid (SA)) copolymer into a container, add 100ml of dichloromethane, dissolve and mix well, then add 20mg Oxaliplatin, shake again and dry in vacuo to remove organic solvent. The dried solid composition is shaped immediately, subpackaged and sterilized by radiation to obtain an anti-solid tumor pharmaceutical composition containing 20% oxaliplatin. 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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