Slow-releasing injection contg. platinum compound and cytotoxin type anticarcinogen
A sustained-release injection and compound technology, applied in the field of medicine, can solve problems such as difficult operation, poor curative effect, and many complications
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Embodiment 1
[0113] Put 80mg of polyphenylpropane (p-CPP: 20:80 of sebacic acid (SA)) copolymer into a container, add 100ml of dichloromethane, dissolve and mix well, then add 10mg Paclitaxel and 10 mg Epplatin were re-shaken and spray-dried to prepare microspheres for injection containing 10% Paclitaxel and 10% Epplatin. Then suspend the microspheres in physiological saline containing 15% mannitol to prepare the corresponding suspension-type sustained-release injection with a viscosity of 220cp-460cp (at 20°C-30°C). The drug release time of the slow-release injection in physiological saline in vitro is 10-15 days, and the drug release time in mice subcutaneous is about 20-30 days.
Embodiment 2
[0115] The method step of being processed into sustained-release injection is the same as that of Example 1, but the difference is that the contained anti-cancer active ingredients and their weight percentages are: 2-40% camptothecin, procarbazine, paclitaxel, and tumor , Cyclophosphamide, Carmustine, Nimustine, Irinotecan, Vincristine, Leuprolide, Colchicine, Aminotriazole, Butylthionine Thioxime, O6-Benzylguanine Or O4-benzylfolate in combination with 2-40% Eriplatin, Sciplatin, Dicycloplatin, Cisliplatin or Picoplatin.
[0116] The excipients used are: racemic polylactic acid, racemic polylactic acid / glycolic acid copolymer, monomethyl polyethylene glycol / polylactic acid, monomethyl polyethylene glycol / polylactic acid copolymer, polyethylene glycol / polylactic acid, polyethylene glycol / polylactic acid copolymer, carboxyl-terminated polylactic acid or carboxyl-terminated polylactic acid / glycolic acid copolymer; the viscosity of the sustained-release injection is 10cp-650cp (...
Embodiment 3
[0118] Put 70 mg of polylactic acid (PLGA, 75:25) with a peak molecular weight of 65,000 into a container, add 100 ml of dichloromethane, dissolve and mix well, add 15 mg of sibplatin and 15 mg of nimustine, re-shake and dry in vacuum Remove organic solvents. The dried drug-containing solid composition was frozen and pulverized to make a micropowder containing 15% subplatin and 15% nimustine, and then suspended in physiological saline containing 1.5% sodium carboxymethylcellulose to prepare the corresponding mixed Suspension-type sustained-release injection with a viscosity of 300cp-400cp (at 20°C-30°C). The drug release time of the slow-release injection in physiological saline in vitro is 10-15 days, and the drug release time in mice subcutaneous is about 20-30 days.
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