Scaffold with copper carboxymethyl chitosan-sodium alginate and preparation method thereof and applications
A technology of carboxymethyl chitosan and sodium alginate, applied in medical science, tissue regeneration, prosthesis, etc., can solve problems such as uneven distribution of copper ions, immediate cross-linking of solutions, and limitations in practical applications, and achieve good antibacterial properties Effect, good biocompatibility, simple preparation process
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Embodiment 1
[0037] Prepare 10 mL of nano-copper solution with a concentration of 10 mM in ultrapure water, and stir with a magnetic stirrer at room temperature until uniform. Gradually add 150 mg of carboxymethyl chitosan and 150 mg of sodium alginate, and stir with a magnetic stirrer at room temperature until completely dissolved. The above mixed solution was added to a 48-well culture plate, and placed in a -80°C refrigerator overnight. The 48-well plate was transferred to a lyophilizer for 48 h. Add 2% CaCl 2 The solution was cross-linked for 30 minutes, and washed three times with ultrapure water. Put it into a -80°C refrigerator and freeze it overnight, and use a freeze dryer to freeze-dry for 24 hours to obtain a scaffold, which is a copper-containing carboxymethyl chitosan-sodium alginate scaffold.
[0038] Combine the resulting bracket with 10 5 Fibroblasts L929 were co-cultured, the medium was discarded at 1, 3, and 5 days, and 10% MTT solution was added. After 4 hours, DMSO ...
Embodiment 2
[0044] Prepare 10mL nano-copper solution with a concentration of 1mM in ultrapure water, and stir with a magnetic stirrer at room temperature until uniform. Gradually add 150 mg of carboxymethyl chitosan and 150 mg of sodium alginate, and stir with a magnetic stirrer at room temperature until completely dissolved. The above mixed solution was added to a 48-well culture plate, and placed in a -80°C refrigerator overnight. The 48-well plate was transferred to a lyophilizer for 48 h. Add 2% CaCl 2 The solution was cross-linked for 30 minutes, and washed three times with ultrapure water. Put it into a -80°C refrigerator and freeze it overnight, and use a freeze dryer to freeze-dry for 24 hours to obtain a scaffold, which is a copper-containing carboxymethyl chitosan-sodium alginate scaffold.
[0045] Compared with the blank culture plate, the copper-containing carboxymethyl chitosan-sodium alginate scaffold prepared in this example had relative cell viability of 85.81%, 132.19%...
Embodiment 3
[0049] Prepare 10mL nano-copper solution with a concentration of 0.1mM in ultrapure water, and stir with a magnetic stirrer at room temperature until uniform. Gradually add 150 mg of carboxymethyl chitosan and 150 mg of sodium alginate, and stir with a magnetic stirrer at room temperature until completely dissolved. The above mixed solution was added to a 48-well culture plate, and placed in a -80°C refrigerator overnight. The 48-well plate was transferred to a lyophilizer for 48 h. Add 2% CaCl 2 The solution was cross-linked for 30 minutes, and washed three times with ultrapure water. Put it into a -80°C refrigerator and freeze it overnight, and use a freeze dryer to freeze-dry for 24 hours to obtain a scaffold, which is a copper-containing carboxymethyl chitosan-sodium alginate scaffold.
[0050] Compared with the blank culture plate, the copper-containing carboxymethyl chitosan-sodium alginate scaffold prepared in this example had relative cell viability of 94.97%, 133.8...
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