Application of non-specific fluorescent dyes for monitoring enantio-selective ligand binding to molecularly imprinted polymers

DOI to cite this document:

10.5283/epub.21068 Copy

Piletsky, Sergey A. ; Terpetschnig, Ewald ; Andersson, Håkan S. ; Nicholls, Ian A. ; Wolfbeis, Otto S.

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Date of publication of this fulltext: 06 Jun 2011 13:19

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Details

Item type:	Article
Journal or Publication Title:	Fresenius' Journal of Analytical Chemistry
Publisher:	Springer
Volume:	364
Number of Issue or Book Chapter:	6
Page Range:	pp. 512-516
Date:	1999
Institutions:	Chemistry and Pharmacy > Institut für Analytische Chemie, Chemo- und Biosensorik > Chemo- und Biosensorik (Prof. Antje J. Bäumner, formerly Prof. Wolfbeis)
Identification Number:	Value Type 10.1007/s002160051377 DOI
Dewey Decimal Classification:	500 Science > 540 Chemistry & allied sciences
Status:	Published
Refereed:	Unknown
Created at the University of Regensburg:	Unknown
Item ID:	21068

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Abstract

The displacement of non-specific dyes from molecularly imprinted polymer (MIP) chromatographic stationary phases has been used for the detection and quantification of ligand-polymer binding events. A blank polymer and an L-phenylalaninamide-imprinted polymer were prepared using methacrylic acid as the functional monomer and ethylene glycol dimethacrylate as a crosslinker. The MIP is first loaded ...

Abstract

The displacement of non-specific dyes from molecularly imprinted polymer (MIP) chromatographic stationary phases has been used for the detection and quantification of ligand-polymer binding events. A blank polymer and an L-phenylalaninamide-imprinted polymer were prepared using methacrylic acid as the functional monomer and ethylene glycol dimethacrylate as a crosslinker. The MIP is first loaded with dye, and a solution of the dye in the eluent is passed through the MIP. If analyte is injected into the dye solution in the eluent, part of the dye is competitively replaced by the analyte from the MIP. Specifically, the competitive displacement of rhodamine B by amino acids and phenylalaninamide (Phe-NH2), respectively, has been studied under polar and hydrophobic elution conditions. Enantioselective binding of Phe and Phe-NH2 to the imprinted polymer was shown to occur in the micromolar concentration range. It is proposed that the displacement of non-specific dyes from MIPs be used for the development of multisensors based upon these highly specific and stable materials, which provide promising alternatives to the use of biological macromolecules in sensor technology.

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Metadata last modified: 26 Nov 2020 06:40

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