A kind of preparation method of environmentally sensitive polymer/gold hybrid dressing
An environmentally sensitive, polymer technology, applied in the directions of non-active ingredients medical preparations, active ingredients-containing medical preparations, drug combinations, etc., can solve the problems of poor water solubility, low bioavailability, and difficult adsorption of curcumin, etc. To achieve the effect of increasing the drug load, prolonging the action time, and improving the utilization rate
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Embodiment 1 3
[0049] The synthesis of embodiment 1 trityl mercaptoglycerol monomer
[0050] Add thioglycerol: triphenylchloromethane: triethylamine into a two-neck flask at a molar ratio of 1.05:1:1.1, and react overnight at room temperature with tetrahydrofuran as a solvent. After TLC showed that the reaction was complete, wash 3 times with deionized water, 3 times with saturated sodium bicarbonate solution, 3 times with saturated sodium chloride solution, collect the organic phase, add anhydrous sodium sulfate to dry for 3 hours, and remove anhydrous sodium sulfate by suction filtration , the solvent was removed by rotary evaporation, purified by silica gel column (eluent: petroleum ether: ethyl acetate = 1:1), the product was collected, the solvent was removed, and vacuum-dried. To obtain product I, the structural formula is:
[0051]
Embodiment 2
[0052] Embodiment 2 polycurcumin prodrug (polymer Ⅱ) is synthesized
[0053] Add curcumin: polyethylene glycol: product Ⅰ into a two-necked bottle at a molar ratio of 1:1:1, dissolve in anhydrous tetrahydrofuran, and then place the anhydrous tetrahydrofuran solution dissolved in oxalyl chloride in a constant pressure dropping funnel , sealed, N-filled 2 Protected and placed in an ice bath, add 3.5 parts of anhydrous triethylamine to the two-necked bottle with a syringe, stir for 5 minutes, then open the constant pressure dropping funnel and slowly add the oxalyl chloride tetrahydrofuran solution into the reaction system, and magnetically stir at room temperature React overnight. After the reaction, filter, concentrate, redissolve with dichloromethane, and wash twice with deionized water, twice with saturated sodium bicarbonate solution, twice with saturated sodium chloride solution, collect the organic phase, and dry with anhydrous sodium sulfate 3h. Anhydrous sodium sulfat...
Embodiment 3
[0055] Example 3 polycurcumin prodrug protecting group removal (polymer III)
[0056] Polymer II and triethylsilane were added to the reaction flask, sealed and filled with N 2 Protect and place in an ice bath. Trifluoroacetic acid (TFA:DCM=1:10, volume ratio) dissolved in anhydrous dichloromethane was added with a disposable syringe, and the reaction was performed under magnetic stirring for 0.5 hours at room temperature. After the reaction, the polymer solution was directly precipitated in cold methanol bubbled with nitrogen in advance to remove the removed protecting group triphenylmethane, and dried in vacuum to obtain polymer III. The structural formula is:
[0057]
[0058] Example 4 Gold Nanoparticle Synthesis
[0059] Weigh 30 mg of hypochlorous acid and dissolve it in 200 ml of deionized water, stir and heat. When it is about to boil, quickly add 102 mg of sodium citrate aqueous solution, continue stirring for 20 minutes, then stop heating, naturally cool to ro...
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