Anticancer compound including phosphatidylinositol 3-kinase inhibitor and alkylate
A kinase inhibitor, phosphoinositide technology, applied in the field of anticancer compositions, can solve the problems of enhanced tolerance, treatment failure and the like
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Embodiment 1
[0113] 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 UCN-01, 20mg carmustine, 10mg UCN-01 and 10mg carmustine respectively, reshake and use spray drying method to prepare 20% UCN-01, 20% carmustine , and microspheres for injection with 10% UCN-01 and 10% carmustine. 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 physiological saline in vitro is 60-70 days, and the drug release time in mouse subcutaneous is more than 60 days.
Embodiment 2
[0115] 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:
[0116] (1) 5-40% UCN-01 or UCN-02;
[0117] (2) 1-30% carmustine, nimustine or lomustine; or
[0118] (3) Combination of 5-40% UCN-01 or UCN-02 and 1-30% carmustine, nimustine or lomustine.
Embodiment 3
[0120] 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 polyene UCN-02, 30mg carmustine, 20mg polyene UCN-02 and 10mg carmustine, re-shake and use spray drying method to prepare 30% polyene UCN-02, 30% carmustine Injectable microspheres of Ting, 20% polyene UCN-02 and 10% carmustine. 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 60-65 days, and the drug release time in mice subcutaneous is about 60 days.
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