A kind of cross-linked chitosan hemostatic powder and preparation method thereof
A technology of cross-linking chitosan and hemostatic powder, which is applied in pharmaceutical formulation, surgery, drug delivery and other directions, can solve the problems of large cross-linking degree, poor hemostatic effect, inability to separate out, etc., and achieves mild reaction conditions, improved hemostatic effect, The effect of improving the suction volume
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Embodiment 1
[0038] Weigh 20g of chitosan with a particle size of 24-80 mesh and a degree of deacetylation of 72.12%, add it to 200mL of ethanol, stir and swell at 40°C for 1.0h, then add 5.2mL of lactic acid dropwise under stirring, 40 Stir and react at ℃ for 1.0h, then raise the temperature to 50℃, add 0.02mL ethylene glycol diglycidyl ether dropwise, stir and react for 5h, after the reaction is completed, filter, wash and dry to obtain the cross-linked chitosan hemostatic powder. Product form see figure 1 .
Embodiment 2
[0040] Weigh 20g of chitosan with a particle size of 24-80 mesh and a degree of deacetylation of 72.12%, add it to 200mL of ethanol, stir and swell at 40°C for 1.0h, then add 6.0mL of lactic acid dropwise under stirring, 40 Stir and react at ℃ for 3.0h, then adjust the temperature to 30°C, add 0.05mL ethylene glycol diglycidyl ether dropwise, stir and react for 6h, after the reaction is completed, filter, wash and dry to obtain the cross-linked chitosan hemostatic powder.
Embodiment 3
[0042] Weigh 20g of chitosan with a particle size of 24-80 mesh and a deacetylation degree of 72.12%, add it to 200mL of isopropanol, stir and swell at 40°C for 3.0h, then add 4.0mL of acetic acid dropwise under stirring , stirred and reacted at 40°C for 0.5h, then added dropwise 0.2mL 1,4-butanediol diglycidyl ether at 40°C, stirred and reacted for 4h, after the reaction was completed, filtered, washed, and dried to obtain cross-linked chitosan Sugar hemostatic powder.
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