| Literature DB >> 17165828 |
Andrew J Hall1, Milena Quaglia, Panagiotis Manesiotis, Ersilia De Lorenzi, Börje Sellergren.
Abstract
A range of 2-acrylamidopyridines, showing subtle differences in solution binding toward carboxylic acids, has been investigated as functional monomers in molecular imprinting. Imprinting of N-Z-L-glutamic acid with one such monomer is shown to be effective in the creation of a molecularly imprinted polymer (MIP) with recognition properties for its template and also for larger molecules containing glutamic acid residues. In comparison to a MIP prepared via a more "traditional" approach, the new polymeric receptors exhibit reduced nonspecific binding. The new receptors are compared with previously reported urea-based receptors targeting the glutamic acid residue and receptors targeting the pteridine substructure of folic acid.Entities:
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Year: 2006 PMID: 17165828 DOI: 10.1021/ac0615652
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986