Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone

Abstract

This study examined the feasibility of removing dexamethasone (DEX) from aqueous solutions using molecularly imprinted polymers (MIPs). The binding energy, used to evaluate the affinity between imprinted molecule and functional monomer, was calculated for DEX using molecular simulation via the density functional theory method. From this approach, three different functional monomers were tested: methacrylic acid, N-(Hydroxymethyl) acrylamide, and 2-hydroxyethyl methacrylate designated as MIP-DEX1, MIP-DEX2, MIP-DEX3, respectively. All of them were prepared by the precipitation polymerization method, with trimethylolpropane trimethacrylate used as the crosslinker. Moreover, the kinetics of adsorption and adsorption isotherms were evaluated using different models to assess the adsorption mechanisms of DEX on polymers. The results showed that equilibrium between the polymer and DEX is reached at 180 min, with a maximum adsorption capacity of 117.27 mg g−1 for sample MIP-DEX3. The kinetic studies indicated that the adsorption of DEX on the polymers fits very well with the pseudo-second-order kinetic model. Equilibrium data were best described by the Freundlich model, suggesting that the sorption process occurs on a heterogeneous surface of the polymer cavities. The thermodynamic study confirms the role of selectivity cavities, exhibited in the sample MIP-DEX3. Reusability tests and application on real samples suggest that the synthesized polymers are promising adsorbents.