Physical and chemical dual-network hydrogel for subcutaneous filler as well as preparation method and application thereof
A hydrogel and filler technology, applied in the field of physical and chemical double network hydrogel for dermal fillers and its preparation, can solve the problems of skin inflammation and achieve good tissue adhesion and anti-degradation characteristics , Improve the effect of action time
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[0033] A preparation method of physical and chemical double network hydrogel for dermal filler, the method comprises the following steps:
[0034] (1) Dissolve hyaluronic acid in deionized water to form a clear and transparent hyaluronic acid solution, and then add 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) Add N-hydroxysuccinimide (NHS) into the hyaluronic acid solution and stir, then add furfurylamine, after the reaction, dialyze and freeze-dry the above solution to obtain furfurylamine-modified hyaluronic acid; wherein, hyaluronic acid The acid is obtained by biological fermentation or extracted from animal tissues such as cockscombs; the molecular weight of the hyaluronic acid is 5-2000kDa, and the mass concentration of the hyaluronic acid solution is 0.5-10%. The molar ratio between furfurylamine and the repeating unit of hyaluronic acid is (0.05-1):1; the sum of the mass of the catalyst EDC and NHS is 10-100% of the mass of hyaluronic acid;
[003...
Embodiment 1
[0041] Step 1: First dissolve hyaluronic acid (5g) in deionized water (500mL) to form a clear and transparent hyaluronic acid solution, then add 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride (EDC, 1.0g) and N-hydroxysuccinimide (NHS, 0.5g) were added to the above hyaluronic acid solution and stirred for a certain period of time, then furfurylamine (0.5g) was added and reacted for 24 hours, Dialysis and freeze-drying the above solution to obtain furfurylamine-modified hyaluronic acid;
[0042] Step 2: Dissolve the furfurylamine-modified hyaluronic acid obtained in step 1 in deionized water to form a furfurylamine-modified hyaluronic acid solution (1%), then adjust the pH of the solution to acidic (pH=1.5), and then Add maleimide-modified polyethylene glycol (MAL-PEG, 0.5 g) as a cross-linking agent to the above acidic mixed solution. The obtained acidic mixed solution was divided into containers and sealed and frozen for 72 hours, then the container was taken out...
Embodiment 2
[0046] Step 1: First dissolve hyaluronic acid (5g) in deionized water (500mL) to form a clear and transparent hyaluronic acid solution, then add 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride (EDC, 2.0g) and N-hydroxysuccinimide (NHS, 1.0g) were added to the above hyaluronic acid solution and stirred for a certain period of time, then furfurylamine (1.0g) was added and reacted for 24 hours, Dialysis and freeze-drying the above solution to obtain furfurylamine-modified hyaluronic acid;
[0047] Step 2: Dissolve the furfurylamine-modified hyaluronic acid obtained in step 1 in deionized water to form a furfurylamine-modified hyaluronic acid solution (1%), then adjust the pH of the solution to acidic (pH=1.5), and then Add maleimide-modified polyethylene glycol (MAL-PEG, 1.0 g) as a cross-linking agent to the above acidic mixed solution. The obtained acidic mixed solution was divided into containers and sealed and frozen for 72 hours, then the container was taken out...
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