Molecularly imprinted polymers selective for d - and l -phenylalanine have been prepared in water solution using 2-acryloylamido-2,2‘-dimethylpropane sulfonic acid and bisacryloyl β-cyclodextrin as functional monomers, and N,N ‘ -diacryloylpiperazine as cross-linker. Polymer−ligand recognition was evaluated using a combination of HPLC, displacement chromatography and fluorescence spectroscopic studies. HPLC studies revealed that the imprinted polymers possess optimal ligand selectivity in 30% water solution in acetonitrile. The results demonstrate that a balance of hydrophobic and electrostatic interactions is required for ligand recognition by these polymers. The imprinting effect is sufficiently strong to reverse the inherent chiral selectivity of the cyclodextrin molecule.
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Piletsky et al. (1999) studied this question.
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