A kind of anti-tumor macromolecular prodrug complex and its preparation method and application
A technology of macromolecules and complexes, applied in antineoplastic drugs, drug combinations, pharmaceutical formulations, etc., can solve problems such as increased bone marrow toxicity, arteriolar embolism, and the inability to effectively overcome tumor multidrug resistance
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Embodiment 1
[0065] Embodiment 1: Synthesis of low molecular weight heparin-doxorubicin macromolecular prodrug
[0066] Weigh 1 mmol of low molecular weight heparin (LMWH) and add it into 10 mL of formamide, stir magnetically for 1 h until it is completely dissolved, add 1-ethyl-(3-dimethylaminopropyl) carbodiimide ( EDC) and hydroxysuccinimide (NHS), after reacting for 0.5h, slowly add the formamide solution of Boc hydrazine (the molar ratio of LWMH, EDC, NHS, Boc hydrazine is 1:5:5:20 successively), drop The speed is 3 seconds between each drop, after the addition, react at room temperature for 24 hours, precipitate with ice acetone, wash the precipitate repeatedly, and dry in vacuum for 12 hours to obtain the active intermediate of LMWH modified by Boc hydrazine; Disperse the body in 6mL of dichloromethane, add 4mL of trifluoroacetic acid, ultrasonically react for 2h, suction filter to obtain a precipitate, redissolve in water, dialyze for 2d, and freeze-dry to obtain an active intermed...
Embodiment 2
[0067] Embodiment 2: Synthesis of heparin-doxorubicin macromolecular prodrug
[0068] Weigh 1 mmol of heparin (heparin) and add it to 10 mL of formamide, stir magnetically for 1 h until it is completely dissolved, add 1-ethyl-(3-dimethylaminopropyl) carbodiimide (EDC) under the condition of nitrogen protection and ice bath ) and hydroxysuccinimide (NHS), after reacting for 2 hours, slowly drop the formamide solution of Boc hydrazine (the molar ratio of heparin, EDC, NHS, and Boc hydrazine is 1:10:15:60 in turn), and the dropping speed is The interval between each drop is 5 seconds. After the addition, react at room temperature for 24 hours, precipitate with ice acetone, wash the precipitate repeatedly, and dry it in vacuum for 12 hours to obtain the active intermediate of heparin modified by Boc hydrazine; disperse 20 mg of active intermediate of heparin modified by Boc hydrazine In 6mL of dichloromethane, add 4mL of trifluoroacetic acid, ultrasonically react for 2h, suction f...
Embodiment 3
[0069] Embodiment 3: the synthesis of hyaluronic acid-curcumin macromolecular prodrug
[0070] 1mmol hyaluronic acid (HA) and 3mmol curcumin (CUR) were respectively dissolved in a mixed solvent of formamide and N,N-dimethylformamide (v:v=1:1). Under the protection of nitrogen, 5 mmol 1-ethyl-(3-dimethylaminopropyl) carbodiimide (EDC) and 0.5 mmol 4-dimethylaminopyridine (DMAP) were added to the HA solution, and after activating for 1 h, slowly Add CUR solution drop by drop at an interval of 2 seconds. After the dropwise addition, react at room temperature for 48 hours. After the reaction is completed, precipitate with glacial ethyl acetate, wash the precipitate repeatedly, redissolve in water, ultrasonicate the probe for 30 minutes, dialyze for 1 day, and freeze After drying, the hyaluronic acid-curcumin macromolecular prodrug (HA-CUR) is obtained.
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