Molecular Imprinting of Bisphenol A on Silica Skeleton and Gold Pinhole Surfaces in 2D Colloidal Inverse Opal through Thermal Graft Copolymerization
<b> </b>This study successfully fabricated BPA-imprinted poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) (poly(4-VP-co-EGDMA)) quartz crystal microbalance (MIP-QCM) sensors on a silica skeleton surface and gold pinholes of silica inverse opal through surface-initiated atom transf...
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doaj-d00f52702b4f487a9697602742f31cf32020-11-25T03:45:53ZengMDPI AGPolymers2073-43602020-08-01121892189210.3390/polym12091892Molecular Imprinting of Bisphenol A on Silica Skeleton and Gold Pinhole Surfaces in 2D Colloidal Inverse Opal through Thermal Graft CopolymerizationJin Chul Yang0Jinyoung Park1School of Applied Chemical Engineering, Kyungpook National University, 80 Daehak-ro, Buk-gu, Daegu 41566, KoreaSchool of Applied Chemical Engineering, Kyungpook National University, 80 Daehak-ro, Buk-gu, Daegu 41566, Korea<b> </b>This study successfully fabricated BPA-imprinted poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) (poly(4-VP-co-EGDMA)) quartz crystal microbalance (MIP-QCM) sensors on a silica skeleton surface and gold pinholes of silica inverse opal through surface-initiated atom transfer radical polymerization (SI-ATRP). The sensing features of the two MIP films on the structured silica surface and nano-scale local gold surface were investigated by measuring the resonant frequency change (<i>f</i>) in QCM sensors. The <i>f</i> values for the <i>p</i>-MIP (MIP on gold pinholes) and <i>s</i>-MIP films (MIP on silica skeleton surface) were obtained with the <i>f</i> value of −199 4.9 Hz and −376 19.1 Hz, respectively, whereas for <i>p</i>-/<i>s</i>-NIP films, the <i>f</i> values were observed to be −115 19.2 Hz and −174 5.8 Hz by the influence of non-specific adsorption on the surface of the films. Additionally, the imprinting factor (IF) appeared to be 1.72 for <i>p</i>-MIP film and 2.15 for <i>s</i>-MIP film, and the limits of quantitation (LOQ) and detection (LOD) were 54.924 and 18.125 nM (<i>p</i>-MIP film) and 38.419 and 12.678 nM (<i>s</i>-MIP film), respectively. Using the Freundlich isotherm model, the binding affinity of the BPA-imprinted films was evaluated. This was measured in an aqueous solution of BPA whose concentration ranged between 45 and 225 nM. It was found that the <i>p</i>-MIP film (m = 0.39) was relatively more heterogeneous than the <i>s</i>-MIP film (m = 0.33), both of which were obtained from the slope of the linear regressions. Finally, the selectivity of the MIP-QCM sensors for BPA detection was determined by measuring the effect of other analogous chemicals, such as bisphenol F (BPF), bisphenol AP (BPAP), and bisphenol B (BPB), in aqueous solutions. The selectivity coefficients (<i>k</i>*) of the two MIP films had ~1.9 for the <i>p</i>-MIP and ~2.3 for the <i>s</i>-MIP films, respectively. The results reveal that, with respect to signal amplification of the QCM sensors, the s-MIP film has better sensing features and faster detection responses than the <i>p</i>-MIP film.https://www.mdpi.com/2073-4360/12/9/1892colloidal lithographysilica inverse opalgold pinholesbisphenol-AFreundlich isotherm |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jin Chul Yang Jinyoung Park |
spellingShingle |
Jin Chul Yang Jinyoung Park Molecular Imprinting of Bisphenol A on Silica Skeleton and Gold Pinhole Surfaces in 2D Colloidal Inverse Opal through Thermal Graft Copolymerization Polymers colloidal lithography silica inverse opal gold pinholes bisphenol-A Freundlich isotherm |
author_facet |
Jin Chul Yang Jinyoung Park |
author_sort |
Jin Chul Yang |
title |
Molecular Imprinting of Bisphenol A on Silica Skeleton and Gold Pinhole Surfaces in 2D Colloidal Inverse Opal through Thermal Graft Copolymerization |
title_short |
Molecular Imprinting of Bisphenol A on Silica Skeleton and Gold Pinhole Surfaces in 2D Colloidal Inverse Opal through Thermal Graft Copolymerization |
title_full |
Molecular Imprinting of Bisphenol A on Silica Skeleton and Gold Pinhole Surfaces in 2D Colloidal Inverse Opal through Thermal Graft Copolymerization |
title_fullStr |
Molecular Imprinting of Bisphenol A on Silica Skeleton and Gold Pinhole Surfaces in 2D Colloidal Inverse Opal through Thermal Graft Copolymerization |
title_full_unstemmed |
Molecular Imprinting of Bisphenol A on Silica Skeleton and Gold Pinhole Surfaces in 2D Colloidal Inverse Opal through Thermal Graft Copolymerization |
title_sort |
molecular imprinting of bisphenol a on silica skeleton and gold pinhole surfaces in 2d colloidal inverse opal through thermal graft copolymerization |
publisher |
MDPI AG |
series |
Polymers |
issn |
2073-4360 |
publishDate |
2020-08-01 |
description |
<b> </b>This study successfully fabricated BPA-imprinted poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) (poly(4-VP-co-EGDMA)) quartz crystal microbalance (MIP-QCM) sensors on a silica skeleton surface and gold pinholes of silica inverse opal through surface-initiated atom transfer radical polymerization (SI-ATRP). The sensing features of the two MIP films on the structured silica surface and nano-scale local gold surface were investigated by measuring the resonant frequency change (<i>f</i>) in QCM sensors. The <i>f</i> values for the <i>p</i>-MIP (MIP on gold pinholes) and <i>s</i>-MIP films (MIP on silica skeleton surface) were obtained with the <i>f</i> value of −199 4.9 Hz and −376 19.1 Hz, respectively, whereas for <i>p</i>-/<i>s</i>-NIP films, the <i>f</i> values were observed to be −115 19.2 Hz and −174 5.8 Hz by the influence of non-specific adsorption on the surface of the films. Additionally, the imprinting factor (IF) appeared to be 1.72 for <i>p</i>-MIP film and 2.15 for <i>s</i>-MIP film, and the limits of quantitation (LOQ) and detection (LOD) were 54.924 and 18.125 nM (<i>p</i>-MIP film) and 38.419 and 12.678 nM (<i>s</i>-MIP film), respectively. Using the Freundlich isotherm model, the binding affinity of the BPA-imprinted films was evaluated. This was measured in an aqueous solution of BPA whose concentration ranged between 45 and 225 nM. It was found that the <i>p</i>-MIP film (m = 0.39) was relatively more heterogeneous than the <i>s</i>-MIP film (m = 0.33), both of which were obtained from the slope of the linear regressions. Finally, the selectivity of the MIP-QCM sensors for BPA detection was determined by measuring the effect of other analogous chemicals, such as bisphenol F (BPF), bisphenol AP (BPAP), and bisphenol B (BPB), in aqueous solutions. The selectivity coefficients (<i>k</i>*) of the two MIP films had ~1.9 for the <i>p</i>-MIP and ~2.3 for the <i>s</i>-MIP films, respectively. The results reveal that, with respect to signal amplification of the QCM sensors, the s-MIP film has better sensing features and faster detection responses than the <i>p</i>-MIP film. |
topic |
colloidal lithography silica inverse opal gold pinholes bisphenol-A Freundlich isotherm |
url |
https://www.mdpi.com/2073-4360/12/9/1892 |
work_keys_str_mv |
AT jinchulyang molecularimprintingofbisphenolaonsilicaskeletonandgoldpinholesurfacesin2dcolloidalinverseopalthroughthermalgraftcopolymerization AT jinyoungpark molecularimprintingofbisphenolaonsilicaskeletonandgoldpinholesurfacesin2dcolloidalinverseopalthroughthermalgraftcopolymerization |
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