Multifunctional temperature-sensitive gel composite dressing for wound healing and preparation and usage thereof
A temperature-sensitive gel and wound healing technology, applied in medical science, bandages, etc., can solve the problems that hydrogel dressings do not have antibacterial function, hydrogel dressings are difficult to apply evenly, and the wound application effect is not ideal, etc., and achieve excellent mechanical properties. Effects of stability, promotion of wound healing, excellent antibacterial properties
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Embodiment 1
[0040] (1) Dissolve chitosan with a viscosity-average molecular weight of 100,000 in 1-3% acetic acid solution, stir to dissolve, drop in lye to adjust pH=8-10, white precipitate precipitates, soak for 6-12 hours, and filter with suction , washed with deionized water until neutral, drained, added 30-100mL of isopropanol to the white precipitate, stirred evenly, raised the temperature to 50-90°C, and added 1g / mL of 2,3-cyclo Oxypropyltrimethylammonium chloride (Glycidyltrimethylammoniumchloride, GTA) solution, divided into 2 to 4 times, 3 to 8mL each time, and each time is not less than 0.5h, after the addition is completed, continue to react for 8 to 24h, after the reaction , add 200~500mL acetone to precipitate, and vacuum dry to obtain the product 2-hydroxypropyltrimethylammonium chloride chitosan (HTCC).
[0041] (2) Add 10 times molar amount of acetic anhydride to Pluronic F127, dissolve with 50-200mL DMSO, slowly drop it under magnetic stirring, and react at 20°C for 12h....
Embodiment 2
[0051] (1) Weigh 3g of chitosan with a viscosity-average molecular weight of 120,000 (deacetylation degree greater than 95%) and dissolve it in 100mL of 2% acetic acid aqueous solution, stir and dissolve at room temperature, and slowly add 10mL of GTA aqueous solution (1g / mL), continue to react for 1 h, after cooling, slowly drop into ice acetone to precipitate, after the precipitation is completed, let stand at 4 degrees Celsius for 10 h, filter to remove acetone, after drying, react in a Soxhlet extractor with hot ethanol for 24 h, and vacuum dry to obtain quaternary Ammonized chitosan derivatives;
[0052] (2) Take by weighing 60 mg of quaternized chitosan derivatives prepared in step (1), place in a serum bottle, add 1 milliliter of acetic acid-sodium acetate buffer (pH=6.8), heat and stir at 30°C (rotating speed 100~1000 revs / min) dissolving to obtain a quaternized chitosan derivative solution;
[0053] (3) Weigh 1.2 grams of F127-CHO, put it in a beaker and dissolve it...
Embodiment 3
[0060] (1) Weigh 5g of chitosan with a degree of deacetylation greater than 95% and dissolve it in 150mL of 2% acetic acid aqueous solution, stir and dissolve at 80 degrees Celsius, slowly add 17mL of GTA aqueous solution (1g / mL) dropwise with a dropping funnel, and continue the reaction for 2h, After cooling, slowly drop into ice acetone to precipitate, after the precipitation is completed, let it stand at 4 degrees Celsius for 5 hours, filter to remove acetone, and after drying, use hot ethanol to react in a Soxhlet extractor for 48 hours, and vacuum dry to obtain a quaternized chitosan derivative ;
[0061] (2) Take by weighing 50 mg of the quaternized chitosan derivative prepared in step (1), place it in a serum bottle, add citric acid-sodium hydroxide-hydrochloric acid buffer solution (pH=7.0) and stir at room temperature (rotating speed 100 ~1000 rev / min) dissolving to obtain a quaternized chitosan derivative solution;
[0062] (3) Take by weighing 0.9 gram of commercia...
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