Anticancer combination of medication
An anti-cancer drug and composition technology, applied in the directions of drug combinations, anti-tumor drugs, pharmaceutical formulations, etc., can solve the problem of difficulty in forming effective drug concentrations, and achieve the effect of strengthening the anti-cancer effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0046] Put 90mg of PLGA with a molecular weight of 10000 (copolymer of glycolic acid and glycolic acid, the weight ratio of glycolic acid to glycolic acid is 25:75) into a container, add 100ml of dichloromethane, dissolve and mix well, then add 10mg of Nocoda azoles, shake again and dry in vacuo to remove organic solvents. The dried solid composition is shaped immediately, subpackaged and sterilized by radiation to obtain an anticancer drug composition containing 10% by weight of nocodazole.
Embodiment 2
[0048] The method step of being processed into anticancer drug composition is identical with embodiment 1, and difference is that contained active ingredient is:
[0049] 0.01%-10% of cytochalasin, ellipticine chloride, ellipticine ellipticine, ellipticine methyl ellipticine, mitokloramine, mitoradone, mitokanihydrazone, mitonaphthine, Mitohydrazine, Mitoquinone, Mitospex, Mitotane, Mitonamamine, Mitozolid, Mitoransone, Colchicine, Salicylate, Colchicine, Colchicine, Norcolchicine, Thio-colchicine, Colcemid, Colchicamide, Colchicine, Norcolchicine, Thio-colchicine, Colchicine, Colchicamide, Colchicine, Cytochalasin, naphthyl carbamate, naphthol, α-naphthol, β-naphthol, α-naphthol phosphate, alcodazole, procodazole, giradazole, or malonic acid (salt ). The above are percentages by weight.
Embodiment 3
[0051] Put 80 mg of pharmaceutical excipient ethylene vinyl acetate copolymer (EVAc) into a container, add 100 ml of dichloromethane to dissolve and mix well, add 20 mg of β-naphthol, shake again, and then vacuum dry to remove the organic solvent. The dried solid composition is shaped immediately, subpackaged and sterilized by radiation to obtain an anticancer drug composition containing 20% by weight of beta-naphthol. The drug release time of the anticancer drug composition in the physiological saline in vitro is 14-24 days, and the drug release time in the mouse subcutaneous is 20-35 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