Slow release injection containing platinum compound and alkylating agent
A technology of sustained-release injections and compounds, applied in the field of medicine, can solve problems such as increased tolerance and treatment failure
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Embodiment 1
[0111] Put 80, 80 and 80 mg of p(BHET-EOP / TC) (BHET-EOP: TC is 80: 20) copolymers into three containers of A, B and C respectively, and then add 100 ml of dichloromethane to each , after dissolving and mixing, add 20mg cisplatin, 20mg carmustine, 10mg cisplatin and 10mg carmustine respectively, and prepare 20% cisplatin, 20% carmustine, And 10% cisplatin and 10% carmustine microspheres for injection. Then suspend the microspheres in physiological saline containing 15% mannitol to prepare the corresponding suspension-type sustained-release injection. The drug release time of the sustained release injection in the physiological saline in vitro is 60-65 days, and the drug release time in the mouse subcutaneous is more than 60 days.
Embodiment 2
[0113] The method step of being processed into slow-release injection is identical with embodiment 1, but difference is that the p(BHET-EOP / TC) that used adjuvant is 50: 50, containing anticancer active ingredient and weight percent thereof are:
[0114] (1) 2-30% carmustine or nimustine;
[0115] (2) 5-40% cisplatin, nedaplatin, or carboplatin; or
[0116] (3) Combination of 5-40% cisplatin, nedaplatin or carboplatin and 1-20% carmustine or nimustine.
Embodiment 3
[0118] Put 70 mg of p(LAEG-EOP) with a peak molecular weight of 10,000-25,000 into three containers of A, B, and C respectively, and then add 100 ml of dichloromethane to each, dissolve and mix well, and pour into the three containers respectively Add 30mg of cisplatin, 30mg of nimustine, 25mg of cisplatin and 5mg of nimustine, re-shake and use the spray drying method to prepare 30% cisplatin, 30% nimustine, 25% cisplatin and 5% Nimustine microspheres for injection. The dried microspheres are suspended in physiological saline containing 1.5% sodium carboxymethylcellulose to prepare the corresponding suspension-type sustained-release injection. The release time of the slow-release injection in physiological saline in vitro is 65-70 days, and the release time in mice subcutaneously is about 65 days.
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