A surface imprinted preparation method for highly selective recognition of ciprofloxacin
A ciprofloxacin, surface imprinting technology, applied in chemical instruments and methods, other chemical processes, etc., can solve the problem of poor adsorption-desorption kinetic performance, deep embedding of active sites, mass transfer and charge transfer The problem of slow kinetic rate, etc., achieves the effect of significant separation effect, reduction of non-specific adsorption, and low price.
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Embodiment 1
[0031] (1) Preparation of ciprofloxacin surface imprinted polymers (MIPs)
[0032] Put 0.2g of active dry yeast into a 100ml round bottom flask, add 10ml of water, mix until the yeast dissolves, then add 40ml of acetonitrile, sonicate for 10min, then add 0.0625mmol of ciprofloxacin, 0.25mmol of acrylamide, and Alcohol di(methacrylate) ester 1mmol, mix and stir, pass nitrogen for 15min, then carefully add 0.0043g of 2,2'-azobisisobutyronitrile, seal the bottle mouth, put it in a water bath shaker, set the temperature 50°C, rotating speed 180rpm, react for 2h, then increase the temperature to 60°C, continue to react for 22h. Then centrifuge and dry under vacuum at 60°C for 12h. The synthesized product was Soxhlet-extracted for 48 hours with a mixture of 90 mL methanol and 10 mL acetic acid to remove the template molecule ciprofloxacin. Finally, the ciprofloxacin surface imprinted polymer was prepared by vacuum drying at 50°C for 6 hours.
[0033] The corresponding non-imprint...
Embodiment 2
[0042] (1) Preparation of ciprofloxacin surface imprinted polymers (MIPs)
[0043] Put 0.15g of active dry yeast into a 100ml round bottom flask, add 10.5ml of water, mix until the yeast dissolves, then add 42ml of acetonitrile, ultrasonication for 10min, then add ciprofloxacin 0.05mmol, acrylamide 0.3mmol, ethyl 1.5 mmol of diol di(methacrylate) ester, mixed and stirred, passed nitrogen for 15 minutes, then carefully added 0.0096 g of 2,2'-azobisisobutyronitrile, sealed the bottle mouth, and put it in a water bath shaker, Set the temperature at 50°C, rotate at 180rpm, react for 2 hours, and increase the temperature to 60 oC , Continue to react for 22h. Then centrifuge and dry under vacuum at 60°C for 12h. The synthesized product was Soxhlet-extracted for 48 hours with a mixture of 90 mL methanol and 10 mL acetic acid to remove the template molecule ciprofloxacin. Finally, the ciprofloxacin surface imprinted polymer was prepared by vacuum drying at 50°C for 6 hours.
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