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Reversible Protein Capture and Release by Redox-Responsive Hydrogel in Microfluidics

Stimuli-responsive hydrogels have a wide range of potential applications in microfluidics, which has drawn great attention. Double cross-linked hydrogels are very well suited for this application as they offer both stability and the required responsive behavior. Here, we report the integration of po...

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Autores principales: Jiao, Chen, Obst, Franziska, Geisler, Martin, Che, Yunjiao, Richter, Andreas, Appelhans, Dietmar, Gaitzsch, Jens, Voit, Brigitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780672/
https://www.ncbi.nlm.nih.gov/pubmed/35054674
http://dx.doi.org/10.3390/polym14020267
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author Jiao, Chen
Obst, Franziska
Geisler, Martin
Che, Yunjiao
Richter, Andreas
Appelhans, Dietmar
Gaitzsch, Jens
Voit, Brigitte
author_facet Jiao, Chen
Obst, Franziska
Geisler, Martin
Che, Yunjiao
Richter, Andreas
Appelhans, Dietmar
Gaitzsch, Jens
Voit, Brigitte
author_sort Jiao, Chen
collection PubMed
description Stimuli-responsive hydrogels have a wide range of potential applications in microfluidics, which has drawn great attention. Double cross-linked hydrogels are very well suited for this application as they offer both stability and the required responsive behavior. Here, we report the integration of poly(N-isopropylacrylamide) (PNiPAAm) hydrogel with a permanent cross-linker (N,N′-methylenebisacrylamide, BIS) and a redox responsive reversible cross-linker (N,N′-bis(acryloyl)cystamine, BAC) into a microfluidic device through photopolymerization. Cleavage and re-formation of disulfide bonds introduced by BAC changed the cross-linking densities of the hydrogel dots, making them swell or shrink. Rheological measurements allowed for selecting hydrogels that withstand long-term shear forces present in microfluidic devices under continuous flow. Once implemented, the thiol-disulfide exchange allowed the hydrogel dots to successfully capture and release the protein bovine serum albumin (BSA). BSA was labeled with rhodamine B and functionalized with 2-(2-pyridyldithio)-ethylamine (PDA) to introduce disulfide bonds. The reversible capture and release of the protein reached an efficiency of 83.6% in release rate and could be repeated over 3 cycles within the microfluidic device. These results demonstrate that our redox-responsive hydrogel dots enable the dynamic capture and release of various different functionalized (macro)molecules (e.g., proteins and drugs) and have a great potential to be integrated into a lab-on-a-chip device for detection and/or delivery.
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spelling pubmed-87806722022-01-22 Reversible Protein Capture and Release by Redox-Responsive Hydrogel in Microfluidics Jiao, Chen Obst, Franziska Geisler, Martin Che, Yunjiao Richter, Andreas Appelhans, Dietmar Gaitzsch, Jens Voit, Brigitte Polymers (Basel) Article Stimuli-responsive hydrogels have a wide range of potential applications in microfluidics, which has drawn great attention. Double cross-linked hydrogels are very well suited for this application as they offer both stability and the required responsive behavior. Here, we report the integration of poly(N-isopropylacrylamide) (PNiPAAm) hydrogel with a permanent cross-linker (N,N′-methylenebisacrylamide, BIS) and a redox responsive reversible cross-linker (N,N′-bis(acryloyl)cystamine, BAC) into a microfluidic device through photopolymerization. Cleavage and re-formation of disulfide bonds introduced by BAC changed the cross-linking densities of the hydrogel dots, making them swell or shrink. Rheological measurements allowed for selecting hydrogels that withstand long-term shear forces present in microfluidic devices under continuous flow. Once implemented, the thiol-disulfide exchange allowed the hydrogel dots to successfully capture and release the protein bovine serum albumin (BSA). BSA was labeled with rhodamine B and functionalized with 2-(2-pyridyldithio)-ethylamine (PDA) to introduce disulfide bonds. The reversible capture and release of the protein reached an efficiency of 83.6% in release rate and could be repeated over 3 cycles within the microfluidic device. These results demonstrate that our redox-responsive hydrogel dots enable the dynamic capture and release of various different functionalized (macro)molecules (e.g., proteins and drugs) and have a great potential to be integrated into a lab-on-a-chip device for detection and/or delivery. MDPI 2022-01-10 /pmc/articles/PMC8780672/ /pubmed/35054674 http://dx.doi.org/10.3390/polym14020267 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jiao, Chen
Obst, Franziska
Geisler, Martin
Che, Yunjiao
Richter, Andreas
Appelhans, Dietmar
Gaitzsch, Jens
Voit, Brigitte
Reversible Protein Capture and Release by Redox-Responsive Hydrogel in Microfluidics
title Reversible Protein Capture and Release by Redox-Responsive Hydrogel in Microfluidics
title_full Reversible Protein Capture and Release by Redox-Responsive Hydrogel in Microfluidics
title_fullStr Reversible Protein Capture and Release by Redox-Responsive Hydrogel in Microfluidics
title_full_unstemmed Reversible Protein Capture and Release by Redox-Responsive Hydrogel in Microfluidics
title_short Reversible Protein Capture and Release by Redox-Responsive Hydrogel in Microfluidics
title_sort reversible protein capture and release by redox-responsive hydrogel in microfluidics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780672/
https://www.ncbi.nlm.nih.gov/pubmed/35054674
http://dx.doi.org/10.3390/polym14020267
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