A kind of responsive medical gel and its preparation method and application
A gel and gelatin technology, applied in the field of medical devices, can solve problems such as wound infection, delayed healing, even complications, and new tissue damage
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Embodiment 1
[0035]The hyperbranched polymer monomer HB-PBAE (such as figure 1 shown). In the reaction, the molar ratio of the active hydrogen of the amino group to the carbon-carbon double bond is 1.2:1, in which PETA and PEGDA700 each provide half of the carbon-carbon double bond.
[0036] The specific operation steps are: Weigh 6.6 grams of dopamine hydrochloride (DOPA•HCl), 6 grams of PETA, 21 grams of PEGDA700 and 80 grams of DMSO solvent, mix thoroughly; add triethylamine (TEA) dropwise to adjust the pH value of the mixture About 8; the mixture was heated in an oil bath, the reaction time was 2.5 h, and the temperature was set at 80°C. Since dopamine is easily oxidized under light, the oil bath device needs to be protected from light; Methyl tert-butyl ether for purification. After the purification once, use a cotton-stuffed funnel to filter out the precipitated unreacted DOPA·HCl, and then purify the filtrate twice with methyl tert-butyl ether; Steam to remove the residual purifyi...
Embodiment 2
[0038] Using 1-vinylimidazole (VI) as raw material, tetraethylthiuram disulfide (DS) as chain transfer agent and azobisisobutyronitrile (AIBN) as initiator, polyvinylimidazole was synthesized by RAFT method. The molar ratio of DS, AIBN and 1-vinylimidazole in the reaction is 1:2:50.
[0039] The specific operation steps are as follows: fully mix 23.53 g of VI, 1.48 g of DS, 1.64 g of AIBN and 100 ml of DMF solvent; pass nitrogen gas into the mixture for at least 30 min, and exhaust the air; heat in an oil bath, and the reaction time is 6 h. The temperature was set at 70°C; after the reaction, the reaction solution was naturally cooled to room temperature; the reaction solution was purified twice with 1000 ml of glacial ether, and then placed in a vacuum drying oven to volatilize the remaining purifying agent, anhydrous ether, to obtain a yellow-brown solid The product, namely PVI.
Embodiment 3
[0041] Dissolve 30 mg of gelatin in 100 μL of PBS (pH 7.4), the temperature of the dissolving water bath is 40°C, and the final concentration of gelatin aqueous solution is 2% (w / v); add HP-PBAE and PVI solutions to the above gelatin aqueous solution sequentially Mix well at room temperature to obtain an aqueous solution of the HP-PBAE / Geln / PVI mixture, and HP-PBAE / Geln / PVI in the aqueous solution of the mixture. Among them, the final concentration of HP-PBAE polymer monomer is 5% (w / v), and the final concentration of PVI is 2.5% (w / v); add ferric chloride solution to the aqueous solution of HP-PBAE / Geln / PVI mixture, quickly Vortex to obtain the gel precursor solution, the added ferric chloride solution concentration is 100mM, the volume of the added ferric chloride solution is 20% of the aqueous solution volume of the HP-PBAE / Geln / PVI mixture; the gel precursor solution Inhale the syringe with the needle removed and expel it quickly and evenly as a gel.
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