Anticancer compound including taxanes and alkylate agent
A technology of a composition and an alkylating agent, which can be used in drug combinations, medical preparations containing active ingredients, antitumor drugs, etc., and can solve problems such as enhanced tolerance and treatment failure.
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Embodiment 1
[0102] 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 paclitaxel, 20mg carmustine, 10mg paclitaxel and 10mg carmustine respectively, shake up again and use spray drying method to prepare 20% paclitaxel, 20% carmustine, and 10% carmustine Paclitaxel 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 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
[0104] 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:
[0105] (1) 5-40% paclitaxel or docetaxel;
[0106] (2) 1-30% carmustine, nimustine or lomustine; or
[0107] (3) Combination of 5-40% paclitaxel and 1-30% carmustine, nimustine or lomustine.
Embodiment 3
[0109] 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 docetaxel, 30mg of carmustine, 20mg of docetaxel and 10mg of carmustine, re-shake and use spray drying method to prepare 30% docetaxel, 30% carmustine, 20% polyene Paclitaxel and 10% carmustine 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 55-65 days, and the release time in mice subcutaneously is about 60 days.
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