Abstract: Novel polymers for dopamine prepared using disulfide templates were developed. The dopamine selective binding sites containing boronic acid and sulfonic groups could be generated. The imprinted polymers showed strong selectivity for dopamine compared to DOPAC, HVA, catechol, tyramine, and epinephrine, since the boronic acid and sulfonic acid in the selective binding sites could strongly interact with di-hydroxyl and amino groups of dopamine, respectively. In this presentation, characterization of the imprinted polymers and effectiveness of the post-imprinted process will be discussed
Template and target information: dopamine