New Journal - Molecular Imprinting (opens in new window)

mips logo Go to mipdatabase.com Search this site:
Custom(Search)
Reference type: Journal
Authors: Rong F, Li P
Article Title: Optimization of S-naproxen imprinted polymers: the combination of theoretical and experimental study.
Publication date: 2011
Journal: High Performance Polymers
Volume: 23
Issue: (8)
Page numbers: 585-591.
DOI: 10.1177/0954008311425973
Alternative URL: http://journals.sagepub.com/doi/abs/10.1177/0954008311425973

Abstract: The interactions between template and functional monomers of molecularly imprinted polymers (MIPs) were studied by ultraviolet and infrared spectral analysis and computer simulation, with S-naproxen as template molecule and methacrylic acid (MAA), acrylamide (AM) and 4-vinyl pyridine (4-VP) as functional monomers, respectively. Then, the S-naproxen imprinted polymers made from three functional monomers were prepared, respectively, and the binding parameters and chiral separation performance of the synthesized MIPs were investigated by Scatchard analysis and thin layer chromatography using MIPs as chiral stationary phase. The results showed that the MIP based on 4-VP possessed the highest imprinting effect while the MIP based on MAA was the lowest, which correlated positively with the interaction strength between template molecule and three monomers. The results of theoretical and experimental studies of S-naproxen imprinted polymers suggested that using spectral analysis and computer aided prediction could promote the synthetic strategy for researching more efficient MIPs.
Template and target information: S-naproxen, naproxen
Author keywords: Molecularly imprinted polymers, functional monomer, binding characteristics, Spectral analysis, computer simulation

Featured products

 

Element 13 card - Aluminium

 

Chemistry ICoN T-shirt

 

Element 102 mug - Nobelium