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Abstract: A novel controllable hydrophilic thermo-responsive molecularly imprinted resin (T-MIR) with a switchable zipper-like architecture was synthesized in the aqueous phase and applied to the selective recognition and extraction of alkaloids by positive temperature regulation. In this synthesis process of T-MIR, 2-acrylamide-2- methylpropanesulfonic acid (AMPS) and acrylamide (AAm) were coupled as zipper-like thermo-responsive monomers, resorcinol, and melamine as hydrophilic monomers, formaldehyde as a cross-linker, and berberine chloride (BerbC) as the template. The resulting T-MIR achieved the controlled rebinding and release of BerbC from temperature stimuli (25-45 °C) and the adsorption process followed the Langmuir isotherm (R2>0.99856) and pseudo-second-order kinetic model (R2>0.98138). The highest theory adsorption ability (33.44 mg/g) and recognition ability (imprinting factor: 4.71) of T-MIR was activated between poly(AMPS) and poly(AAm) in the zipper-like architecture at 35 °C. T-MIR was then applied to the selective recognition alkaloids by dispersive solid phase extraction. The limit of detection and limit of quantitation of the method were less than 0.025 mg/L and 0.082 mg/mL, respectively. The recoveries of the proposed method at three spiked levels were 96.8-100.8%, with a relative standard deviation of less than 4.8%. In contrast to previous thermo-responsive materials, this switchable zipper-like hydrophilic T-MIR with good adsorption, specificity recognition, and excellent temperature controllable properties provides a unique alternative to the selective recognition and controlled rebind-release alkaloids by the temperature signal
Template and target information: alkaloids
Author keywords: Thermo-responsive resin, Controllable, alkaloids, Imprinted