Anticancer composition containing antimetabolism medicament and bortezomib
A bortezomib, anti-metabolism technology, used in drug combinations, active ingredients of boron compounds, anti-tumor drugs, etc., can solve problems such as toxic reactions, inability to effectively kill tumor cells, and sudden release.
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Embodiment 1
[0098] Put 90, 90 and 80mg p(BHET-EOP / TC), BHET-EOP: TC is 80:20) copolymer into three containers of A, B and C respectively, and then add 100 ml of dichloromethane to each , after dissolving and mixing, add 10mg fluorouracil, 10mg bortezomib, 10mg fluorouracil and 10mg bortezomib respectively, reshake and prepare 10% fluorouracil, 10% bortezomib, and 10% fluorouracil and 10 % Bortezomib Microspheres for Injection. Then suspend the microspheres in physiological saline containing 15% mannitol to prepare the corresponding suspension-type sustained-release injection. The release time of the slow-release injection in physiological saline in vitro is 40-50 days, and the release time in mice subcutaneously is more than 50 days.
Embodiment 2
[0100] The method step of being processed into slow-release injection is identical with embodiment 1, but difference is that used auxiliary material is the p(BHET-EOP / TC) of 50: 50, containing anticancer active ingredient and weight percent thereof are:
[0101] (1) 5-30% fluorouracil or cytarabine;
[0102] (2) 5-30% bortezomib; or
[0103] (3) Combination of 5-30% fluorouracil or cytarabine and 5-30% bortezomib.
Embodiment 3
[0105] 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 cytarabine, 30mg bortezomib, 15mg cytarabine and 15mg bortezomib, re-shake and use spray drying method to prepare 30% cytarabine, 30% bortezomib, 15% arabino Microspheres for injection of cytidine and 15% bortezomib. The dried microspheres are suspended in physiological saline containing 1.5% sodium carboxymethylcellulose to prepare the corresponding suspension-type sustained-release injection. The drug release time of the sustained release injection in physiological saline in vitro is 50-65 days, and the drug release time in mice subcutaneous is about 60 days.
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