P-aminobenzoate chitosan ester and preparation method thereof
A technology of chitosan aminobenzoate and p-aminobenzoic acid, which is applied in the field of polymer compounds, can solve the problem of chitosan being insoluble in water, etc., achieve good antibacterial activity and expand the effect of antibacterial range
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Embodiment 1
[0038] Take 1 g of dried p-aminobenzoic acid and put it into a three-neck flask, add 30 mL of anhydrous ether, then add 2 mL of thionyl chloride, put it into an ultrasonic scrubber with a water temperature of 30 ° C, react for 10 minutes, cool, pump P-aminobenzoyl chloride was obtained by filtration.
[0039] Add 1g chitosan to 20mL mass fraction 3% glacial acetic acid to swell for 30min, transfer to a 250ml three-neck flask, add 10mL absolute ethanol, stir, and add 1.5mL dissolved in 30ml absolute ethanol to the constant pressure dropping funnel The benzaldehyde in the solution was reacted at 40°C for 5 hours, flocculent solids appeared, added 200mL of ethanol and stood overnight, filtered with suction, washed with a mixture of 20mL of ethanol and 20mL of ether, and dried at constant temperature to obtain a light yellow solid, namely Schiff's base.
[0040] Add 0.5g of the prepared chitosan Schiff base into a 250ml three-neck flask, and add 15mL of isopropanol and pyridine mi...
Embodiment 2
[0043] The bacteriostasis efficiency (%) of resulting product p-aminobenzoic acid chitosan ester of the present invention and chitosan to staphylococcus aureus
[0044]
Embodiment 3
[0046] The bacteriostasis efficiency (%) of resulting product p-aminobenzoic acid chitosan ester of the present invention and chitosan to Aspergillus niger
[0047]
[0048] The method for measuring the above antibacterial efficiency: prepare chitosan solutions and derivative solutions with different mass fractions (using 0.5% acetic acid solution as solvent). 0.1 mL of bacterial suspension and 0.1 mL of sample solutions of different concentrations were evenly spread on the medium plate, and the blank was the bacterial suspension without sample solution. All the plates were cultured in a constant temperature incubator at 37 °C for 24 h, and the growth of bacteria on each plate was observed, and the inhibition rate was calculated:
[0049] I = (n 1 -n 2 ) / n 1 ×100%
[0050] Among them, n 1 and n 2 are the number of colonies on blank and sample-coated plates, respectively.
[0051] For Aspergillus niger, the antibacterial efficiency of chitosan and its derivatives was ...
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