Molecularly imprinted polymers (MIPs) are typically synthesized in organic solvents, leading to poor compatibility with water, weak affinity and selectivity for target molecules in aqueous media. To address these challenges, a green and sustainable synthesis of sandwich bread-like ATP@MIP was conducted using polyethylenimide (PEI) and deep eutectic solvent (DES) as hydrophilic bi-functional monomers via layer-by-layer self-assembly on the attapulgite (ATP) carrier. The new ATP@MIP can provide a higher density of imprinting sites with more orderly and uniform distribution due to inhibiting the competitive polymerization between PEI and DES, thereby significantly enhancing recognition ability. Moreover, the ATP@MIP was synthesized in water, aligning with green chemistry principles and establishing a sustainable preparation method for MIP materials. Equipped with the remarkable merits of good water compatibility, excellent selectivity (IF=3.6), high adsorption capacity (77.6 mg g-1) and desirable repeatability (8 times), the as-prepared materials were used as a solid phase extraction adsorbent for efficient separation and enrichment of baicalin from Scutellariae Radix. More importantly, the recognizing performance of ATP@MIP for baicalin increased 1.40-1.69 times than other MIP materials, and its excellent specificity was demonstrated in comparison with several common commercial adsorbents (C18, HLB, MCX and SAX). Therefore, this work introduces a feasible and green strategy to synthesize water-compatible MIP materials for highly selective enrichment and separation of active components from natural products.
Keywords: Green synthesis; Molecularly imprinted polymer; Template immobilization; Water-compatible.
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