Modifier, preparation method and use method thereof, and medical material
A technology of modifiers and substrates, applied in the field of medical materials and modifiers, can solve the problems of weak binding between polymers and substrates, limited application range of substrates, unfavorable long-term use, etc., and achieve good cell compatibility, Good for grooming and avoiding pollution effects
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preparation example Construction
[0066] The embodiment of the present invention also provides a method for preparing a modifier, comprising:
[0067] The dopamine derivative modified with an active alkenyl group and the zwitterionic compound with an active alkenyl group or the zwitterionic derivative compound modified with an active alkenyl group undergo a free radical-initiated carbon-carbon addition reaction under the action of an initiator.
[0068] The modifying agent in the embodiment of the present invention is formed by polymerizing the dopamine derivative modified with an active alkenyl group and the zwitterionic compound through a carbon-carbon double bond free radical polymerization reaction. The zwitterionic compound itself may carry a reactive alkenyl group, or the alkenyl group may be modified by additional steps. The synthesis route of the modifier is short, the conditions are mild, and the functional groups of dopamine and zwitterionic compounds are not destroyed, the production of by-products ...
Embodiment 1
[0106] (1) Add 18g of sodium pyroborate and 8g of sodium bicarbonate into 200ml of deionized water and stir to dissolve, then filter out the insoluble matter, pass nitrogen into the aqueous solution to remove dissolved oxygen, then put 10g of dopamine hydrochloride into the aqueous solution and stir to dissolve it , appropriately add 0.2mol / L NaOH solution to adjust the pH to above 8, and then pass nitrogen gas for treatment for ten minutes.
[0107] (2) Add 9.4ml of methacrylic anhydride into 50ml of THF and stir evenly, then add dropwise into the solution obtained in step (1), then maintain nitrogen atmosphere, and stir overnight at room temperature.
[0108] (3) Adjust the pH of the solution obtained in step (2) to below 2 with 0.2 mol / L hydrochloric acid solution, and wash off the oily drop-like substance in the upper layer with a small amount of ethyl acetate. The solution was extracted and separated three times with 200 ml of ethyl acetate, and the ethyl acetate phase (t...
experiment example 1
[0113] Experimental example 1 antibacterial test
[0114] The unirritated saliva of healthy blood donors was collected, the supernatant was collected after centrifugation, and pasteurized at 60°C for 30 minutes. Add sterilized PBS to the sterilized saliva at a ratio of 1:1 to obtain a nutrient solution. Soak the medical material with the nutrient solution overnight at 37°C.
[0115] Streptococcus mutans UA-159 was used for antibacterial test. The strain was first incubated at 37 °C in CO 2 After culturing in the incubator for 48 hours, take a single strain and inoculate it in BHI (brain heart infusion) culture solution, and then incubate at 37°C, CO 2 conditions overnight. Place the medical materials treated with nutrient solution in a 12-well plate, inoculate 2mL of BHI culture solution and 40μL of Streptococcus mutans suspension in each well, and inoculate at 37°C in CO 2 cultured in an incubator. After culturing for 15 hours, the morphology and distribution of bacteri...
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