Tsiklomitsin molecular engram integral column preparation method
A molecular imprinting and monolithic column technology, applied in the field of bioengineering, can solve the problems of high false positive and long time consumption, and achieve the effect of fast mass transfer rate, low back pressure and good molecular recognition performance.
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example 1
[0027] First, 0.1 mmol of template molecule tetracycline TC was dissolved in 20 mmol of methanol by ultrasonic, and 0.8 mmol of porogen (cyclohexanol 1.10 g) functional monomer MAA was added to interact for 6 h to form a complex, and then 4 mmol of cross-linking agent EDMA was added. (TC:MAA:EDMA=1:8:40), initiator AIBN 20mg, the solution was ultrasonically degassed for 5-10min, passed nitrogen for deoxygenation for 20min, then the mixture was injected into a 10cm stainless steel column, thermally induced at 60°C Water bath reaction for 12h. The prepared molecularly imprinted monolithic column was connected to a high-pressure infusion pump and washed with methanol and acetonitrile / acetic acid (94:6, v / v) solution to remove porogen and template molecules to obtain polymer 1 (MIP1).
example 2
[0029] A porogen (1.10 g of dodecanol) was added, and others were the same as in Example 1 to obtain MIP2.
example 3
[0031] The porogen (0.20 g of cyclohexanol and 0.90 g of dodecanol) was added, and others were the same as in Example 1 to obtain MIP3.
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