During the evaluation of molecular imprinted polymers (MIPs) prepared again
st the drug tamoxifen a propranolol-derived MIP was used as a positive cont
rol. Surprisingly the propranolol-derived MIP showed considerable selectivi
ty towards tamoxifen, and was indeed much more selective than the MIP prepa
red using tamoxifen as the imprint molecule. The consequences of this unexp
ected, cross reactivity for the use of MIPs in analytical chemistry is disc
ussed.