Slow released anticancer combination of medication embedded the interior of the body
An anti-cancer drug and composition technology, which can be used in drug combination, drug delivery, anti-tumor drugs, etc., and can solve problems such as local formation of effective drug concentration in difficult tumors
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0042] Put 90 mg of polylactic acid (hole A) with a molecular weight of 10,000 in a container, add 100 ml of dichloromethane, dissolve and mix, add 10 mg of ifosfamide, shake again, and vacuum dry to remove the organic solvent. The dried solid composition is formed immediately, and then sterilized by radiation after being packaged to obtain an anticancer pharmaceutical composition containing 10% by weight of ifosfamide. The release time of the anticancer drug composition in physiological saline in vitro is 15-20 days, and the release time of the anticancer drug composition in subcutaneous mice is 30-40 days.
Embodiment 2
[0044] The method steps of being processed into the anticancer pharmaceutical composition are the same as those in Example 1, the difference is that the active ingredients contained are:
[0045] 5-30% by weight of three mustards, cyclophosphamide, sulfophosphamide, diphosphamide, horse phosphoramide, pephosphamide, trophosphamide, carbazole sulfamide, azomethine, amethanone, thymopentin, chlorine Mifen, Letrozole, Sodium Cantharidinium, Cantharidin, Sodium Cantharidin, Methyl Cantharidide, Hydroxycantharidin, Norcantharidin, Thiocolch, Racemic Phenylalanine Chlorine, Melasquin, Diantriazole, Mannosufan, Triosulfan, Ritrasuvan, Improsulfan, Mefenfenfoss, Spirobromopropamide, Mannitol Disulfonate, Triazinazolamide, Enprobamate, Epiperidine, butenolimine, ethidium bismorpholine, ethidoxyurea, ethidium, etoroglu, phosphoammonium, dipropoxyimine quinone, pipepobromane, piperosulfan, Pilitraxine, Bisantron, Bisantron, Rezosufang, Sodium Cyclohexyl Succinate, Rofecoxib, Aspicone, T...
Embodiment 3
[0047] Put 80 mg of polyglycolic acid and glycolic acid copolymer (PLGA) with a molecular weight of 10000 into a container, add 100 ml of dichloromethane, dissolve and mix, add 20 mg of letrozole, shake again, and then vacuum dry to remove the organic solvent . The dried solid composition is formed immediately, and then sterilized by radiation after being divided into packages to obtain an anticancer pharmaceutical composition containing 20% by weight of letrozole. The drug release time of the anticancer drug composition in vitro in physiological saline is 15-20 days, and the drug release time in mice subcutaneously is 30-40 days.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com