Anticancer composition loaded with bortezomib and alkyl agent
A technology of bortezomib and alkylating agent, applied in boron compound active ingredient, drug combination, anti-tumor drug and other directions, can solve the problems of ineffective killing of tumor cells, slow drug release, toxic reaction, etc.
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Embodiment 1
[0109] 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 bortezomib, 10mg melphalan, 10mg bortezomib and 10mg melphalan respectively, shake up again and use spray drying method to prepare 10% bortezomib, 10% melphalan, and microspheres for injection with 10% bortezomib and 10% melphalan. Then suspend the microspheres in physiological saline containing 15% mannitol to prepare the corresponding suspension-type sustained-release injection. The release time of the sustained-release injection in physiological saline in vitro is 60-70 days, and the release time in mouse subcutaneous colon cancer is more than 60 days.
Embodiment 2
[0111] 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:
[0112] 5-30% bortezomib with 5-30% melphalan, cyclophosphamide, ifosfamide, 4H-peroxycyclophosphamide, norcantharidin, desphosphamide, mafosfamide, or pefosfamide combination of amides.
Embodiment 3
[0114] 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 bortezomib, 30mg cyclophosphamide, 15mg bortezomib and 15mg cyclophosphamide, shake up again and use spray drying method to prepare 30% bortezomib, 30% cyclophosphamide, 15% bortezomib and 15 % cyclophosphamide injection microspheres. 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 sustained-release injection in physiological saline in vitro is 65-75 days, and the release time in mouse subcutaneous lung cancer is about 65 days.
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