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...

Full description

Bibliographic Details
Main Authors: Jin Chul Yang, Jinyoung Park
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Polymers
Subjects:
Online Access:https://www.mdpi.com/2073-4360/12/9/1892
id doaj-d00f52702b4f487a9697602742f31cf3
record_format Article
spelling 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
_version_ 1724509106132221952