Modifier, its preparation method, use method and medical material
A technology for modifiers and metal 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 , Conducive to modification, to avoid the effect of pollution
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preparation example Construction
[0066] The embodiment of the present invention also provides a preparation method of the modifier, including:
[0067] The dopamine derivative modified with an active alkenyl group and a zwitterionic compound having an active alkenyl group or a zwitterionic derivative compound modified with an active alkenyl group undergo a free radical-induced carbon-carbon addition reaction under the action of an initiator.
[0068] The modifier of the embodiment of the present invention is formed by polymerizing the dopamine derivative and the zwitterionic compound modified with a reactive alkenyl group through a carbon-carbon double bond radical polymerization reaction. The zwitterionic compound itself may have an active alkenyl group, or the alkenyl group may be modified through additional steps. The synthetic route of the modifier is short, the conditions are mild, and the functional groups of dopamine and zwitterionic compounds are not destroyed, the generation of by-products is reduced, and...
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, pour nitrogen into the aqueous solution to remove the dissolved oxygen, then add 10g of dopamine hydrochloride into the aqueous solution and stir to dissolve , Appropriately add 0.2mol / L NaOH solution to adjust the pH to above 8, and then let in nitrogen for ten minutes.
[0107] (2) Add 9.4 ml of methacrylic anhydride to 50 ml of THF and stir uniformly, and then add dropwise to the solution obtained in step (1), and then maintain a 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 upper layer of oil droplets with a small amount of ethyl acetate. The solution was extracted and separated three times with 200 ml ethyl acetate, and the ethyl acetate phase (the first organic solvent phas...
experiment example 1
[0113] Experimental example 1 Bacteriostatic test
[0114] Collect all non-irritating saliva from healthy blood donors, collect the supernatant after centrifugation, and pasteurize at 60°C for 30 min. Sterilized PBS was added to the sterilized saliva at a ratio of 1:1 to obtain a nutrient solution. The medical material was soaked in the nutrient solution overnight at 37°C.
[0115] Streptococcus mutans UA-159 was used for antibacterial test. The strain was first in 37°C CO 2 After culturing in the incubator for 48 hours, a single strain was inoculated into BHI (brain heart infusion) medium, and then at 37℃, CO 2 Cultivate overnight under the conditions. Place the medical materials treated with nutrient solution in a 12-well plate, and inoculate each well with 2mL BHI culture medium and 40μL Streptococcus mutans suspension, at 37℃ CO 2 Cultivate in an incubator. After culturing for 15 hours, the morphology and distribution of bacteria on the surface of the medical material were c...
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