Sa. Piletsky et al., IMPRINTED MEMBRANES FOR SENSOR TECHNOLOGY - OPPOSITE BEHAVIOR OF COVALENTLY AND NONCOVALENTLY IMPRINTED MEMBRANES, Macromolecules, 31(7), 1998, pp. 2137-2140
New types of polymeric membranes with molecular recognition sites for
L-phenylalanine (L-Phe), 6-amino-1-propyluracil (APU), atrazine, and s
ialic acid have been prepared using the molecular imprinting approach.
The membrane synthesis includes radical polymerization of ethylene gl
ycol dimethacrylate (EDMA) and functional monomers in the presence of
a template. Several compounds(-)-(diethylamino)ethyl methacrylate (DEA
EM), methacrylic acid (MAA), allylamine (AA), and (4-vinylphenyl)-boro
nic acid-were as functional monomers, which are able to form covalent,
ionic, or hydrogen bonds with the corresponding templates. Template s
pecific conductometric sensors, based on these polymers, were construc
ted and studied. An opposite response of covalently versus noncovalent
ly imprinted membranes was demonstrated and discussed in detail. Senso
rs based on these materials could detect the target molecules at conce
ntrations of 1-50 mu M in solution. The high specificity and stability
of these imprinted membranes render them promising alternatives to en
zymes, antibodies, and other natural receptors usually used in sensor
technology.