Chloramphenicol molecular imprinting polymer microballoon with uniformity in size as well as preparation method and application thereof
A technology of molecular imprinting and polymers, applied in alkali metal compounds, chemical instruments and methods, alkali metal oxides/hydroxides, etc., can solve problems such as tailing, low resolution, and broadening of chromatographic peaks
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[0035] Regarding the preparation of molecularly imprinted polymer microspheres, there are many factors that affect the performance of molecularly imprinted polymers, including: template molecule dosage, functional monomer, crosslinking agent, type and dosage of porogen, polymerization temperature, time, and initiator dosage Wait. Therefore, molecularly imprinted polymer microspheres need to investigate multiple conditions.
[0036] The preparation method of the blank polymer used for the control, except that the template molecule chloramphenicol is not added, other conditions are the same as the preparation conditions of the molecularly imprinted polymer microspheres.
Embodiment 1
[0038] First, prepare the dispersed phase solution. Dissolve 1mmol of template molecule CDHB ultrasonically in 5mL of porogen chloroform and ethyl acetate (weight ratio 1:1), add 4mmol of functional monomer 4-vinylpyridine, crosslinker EDMA 19mmol, Initiator azobisisobutyronitrile AIBN 0.20g, the solution is degassed by ultrasonic for 5min, nitrogen is deaerated for 10min, and then the solution is transferred to the syringe of the syringe pump (try to avoid air entering the syringe); prepare a continuous phase solution and disperse Add 0.72 g of PVA to 60 mL of water, stir to dissolve, ultrasonically degas for 5 min, bubbling in nitrogen for 20 min, and place it in a continuous phase container.
[0039] The continuous phase was stirred at 210 rpm and nitrogen gas was introduced. Driven by the syringe pump, the dispersed phase solution enters the square chamber of the microfluidic device through the connecting tube, and then enters the continuous phase through the microchannel, an...
Embodiment 2
[0044] First, prepare the dispersed phase solution. Dissolve 1mmol template molecule CDHB ultrasonically in 6mL of porogen chloroform and ethyl acetate (weight ratio 4:6), add 3mmol functional monomer allylpiperazine, crosslinker EDMA 18mmol, Initiator azobisisobutyronitrile AIBN 0.22g, the solution is degassed by ultrasonic for 5min, nitrogen is deaerated for 10min, and then the solution is transferred to the syringe of the syringe pump (try to avoid air entering the syringe); prepare a continuous phase solution and disperse Add 0.78 g of PVA to 66 mL of water, stir to dissolve, ultrasonically degas for 5 min, bubbling in nitrogen for deoxygenation for 20 min, and place in a continuous phase container.
[0045] The continuous phase was stirred at 230 rpm and nitrogen gas was introduced. Driven by the syringe pump, the dispersed phase solution enters the square chamber of the microfluidic device through the connecting tube, and then enters the continuous phase through the microch...
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