Smart Hydrogel Grating Immunosensors for Highly Selective and Sensitive Detection of Human-IgG
Authors
Zhao, Jia-JiaWang, Wei
Wang, Fang
Zhao, Yu
Cai, Quan-Wei
Xie, Rui
Ju, Xiao-Jie
Liu, Zhuang
Faraj, Yousef
Chu, Liang-Yin
Affiliation
University of Chester; Sichuan UniversityPublication Date
2020-05-08
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A smart diffraction grating immunosensor based on antigen-responsive hydrogel with enhanced analyte-induced volume changes is developed for highly selective and sensitive detection of human immunoglobulin G (H-IgG). The hydrogel grating contains poly(N-isopropylacrylamide) (PNIPAM) backbones with dual-cross-linking based on the dynamic complexation between pendent goat-anti-human IgG (GAH-IgG) and pendent H-IgG, and the covalent bonding by 4-arm-polyethylene glycol-acrylamide. Upon recognizing free H-IgG in the environment, the pendent GAH-IgG in the hydrogel can form new GAH-IgG/H-IgG complexes with free H-IgG because the binding constant of GAH-IgG to the free H-IgG is much larger than that of GAH-IgG to the pendent H-IgG and thus result in the decomplexation of GAH-IgG/H-IgG complexes with the pendent H-IgG as well as the swelling of hydrogel. The thermo-responsive PNIPAM backbones enable enhancement of H-IgG-responsive volume change of the proposed hydrogel grating via temperature regulation. Moreover, the cross-linker 4-arm-polyethylene glycol-acrylamide provides excellent transparency for the PNIPAM backbones during the volume change, which ensures output of diffracted optical signals with high intensity. With the elaborately designed molecular structures, the hydrogel grating allows highly selective and sensitive detection of [H-IgG] with a detection limit as low as 1.3 × 10–8 M. This work provides a simple and flexible strategy for developing diffraction grating immunosensors based on stimuli-responsive hydrogels for efficient detection of biomarkers.Citation
Zhao, J.-J., Wang, W., Wang, F., Zhao, Y., Cai, Q.-W., Xie, R., Ju, X-J., Liu, Z., Faraj, Y., & Chu, L.-Y. (2020). Smart hydrogel grating immunosensors for highly selective and sensitive detection of human-IgG. Industrial & Engineering Chemistry Research, 59(22), 10469-10475. https://doi.org/10.1021/acs.iecr.0c00780Publisher
American Chemical SocietyAdditional Links
https://pubs.acs.org/doi/10.1021/acs.iecr.0c00780Type
ArticleDescription
This document is the Accepted Manuscript version of a Published Work that appeared in final form in [Industrial & Engineering Chemistry Research], copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see [https://pubs.acs.org/doi/10.1021/acs.iecr.0c00780].ISSN
0888-5885EISSN
1520-5045ae974a485f413a2113503eed53cd6c53
10.1021/acs.iecr.0c00780
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Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0/