Enantioselective sensor based on microgravimetric quartz crystal microbalance with molecularly imprinted polymer film

Citation
L. Cao et al., Enantioselective sensor based on microgravimetric quartz crystal microbalance with molecularly imprinted polymer film, ANALYST, 126(2), 2001, pp. 184-188
Citations number
29
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
ANALYST
ISSN journal
00032654 → ACNP
Volume
126
Issue
2
Year of publication
2001
Pages
184 - 188
Database
ISI
SICI code
0003-2654(2001)126:2<184:ESBOMQ>2.0.ZU;2-S
Abstract
We report a novel quartz crystal microbalance sensor that provides enantios electivity to dansylphenylalanine enantiomers by using a molecularly imprin ted polymer film as a recognition element. The polymeric recognition thin f ilm, imprinted with chiral dansyl-l-phenylalanine, was immobilised on a gol d electrode modified with a photoactive precursor monolayer via a self-asse mbly process using photopolymerisation. The fabricated sensor was able to d iscriminate between l- and d-dansylphenylalanine enantiomers in solution ow ing to the enantioselectivity of the imprinted sites. The enantiomeric comp osition of l- and d-enantiomeric mixtures could be quantitatively determine d by the fabricated sensor. The detection limit is 5 mug mL(-1) with a resp onse range of 5-500 mug mL(-1) at pH 10.0. The influence of the template co ncentration on the sensitivity and selectivity of the synthesised polymer m embranes was investigated and optimised. The surface characteristics of the polymer coating were studied by varying the pH value of the buffer solutio n, and a convenient regeneration process was proposed to increase the repro ducibility and reusability of the sensor by flushing with pH 2.0 buffer. Th e selectivity and recognition mechanism of the imprinted polymer film were studied with compounds that are structurally related to the template. The m ethod presented in this work provides a novel means of preparing highly sel ective and sensitive chemical sensors via self-assembly and molecularly imp rinting techniques.