Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties

Biodegradable polymers are pivotal in tissue engineering, facilitating long-term tissue reintegration and reducing the necessity for surgery. However, collagen, a crucial component of the extracellular matrix, encountered challenges due to its limited mechanical strength and rapid in-vivo degradatio...

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Published in:POLYMERS FOR ADVANCED TECHNOLOGIES
Main Authors: Hidayah, Shahemi Nur; Adila, Ahmad Ruzaidi Dania; Sharaniza, Ab Rahim; Abid, Amir Muhammad; Muzamir, Mahat Mohd
Format: Article
Language:English
Published: WILEY 2024
Subjects:
Online Access:https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001290844200001
author Hidayah
Shahemi Nur; Adila
Ahmad Ruzaidi Dania; Sharaniza
Ab Rahim; Abid
Amir Muhammad; Muzamir
Mahat Mohd
spellingShingle Hidayah
Shahemi Nur; Adila
Ahmad Ruzaidi Dania; Sharaniza
Ab Rahim; Abid
Amir Muhammad; Muzamir
Mahat Mohd
Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
Polymer Science
author_facet Hidayah
Shahemi Nur; Adila
Ahmad Ruzaidi Dania; Sharaniza
Ab Rahim; Abid
Amir Muhammad; Muzamir
Mahat Mohd
author_sort Hidayah
spelling Hidayah, Shahemi Nur; Adila, Ahmad Ruzaidi Dania; Sharaniza, Ab Rahim; Abid, Amir Muhammad; Muzamir, Mahat Mohd
Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
POLYMERS FOR ADVANCED TECHNOLOGIES
English
Article
Biodegradable polymers are pivotal in tissue engineering, facilitating long-term tissue reintegration and reducing the necessity for surgery. However, collagen, a crucial component of the extracellular matrix, encountered challenges due to its limited mechanical strength and rapid in-vivo degradation. This study addresses these issues through crosslinking and functionalizing collagen with synthetic 4-arm amine-terminated polyethylene glycol (PEG) in a semi-interpenetrating network (IPN) hydrogel. The first goal is to enhance resistance to hydrolysis, thus extending the biodegradation rate. Then, to explore its electrical conductivity properties for certain applications like neural tissue regeneration. The hydrogels were fabricated using sequential IPN formation synthesis where their structural stability and type of degradation by-products were confirmed using Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, scanning electron microscopy (SEM), and nuclear magnetic resonance (NMR). Next, its mechanical and degradation properties investigations exhibit a 92% enhancement in hardness and a 90% retainment of its initial mass over time under physiological conditions. Additionally, the introduction of polypyrrole (PPy) via in-situ polymerization increases its electrical conductivity, achieving a remarkable 104-fold increase at a 0.75 M concentration, attributed to the interconnectivity of PPy chain networks within the three-dimensional structure of IPN collagen/PEG hydrogel. The increased PPy concentration improves conductivity and reduces energy requirements for redox reactions, ensuring electrochemical stability as revealed by cyclic voltammetry analysis. The demonstrated structural and electrochemical stability of the semi-IPN collagen/PEG/PPy hydrogel within a physiological environment through a facile sequential crosslinking method underscores its promising practical applications in enhancing clinical effectiveness.
WILEY
1042-7147
1099-1581
2024
35
8
10.1002/pat.6546
Polymer Science

WOS:001290844200001
https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001290844200001
title Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
title_short Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
title_full Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
title_fullStr Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
title_full_unstemmed Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
title_sort Sequentially crosslinked collagen-based hydrogel to form a semi-interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
container_title POLYMERS FOR ADVANCED TECHNOLOGIES
language English
format Article
description Biodegradable polymers are pivotal in tissue engineering, facilitating long-term tissue reintegration and reducing the necessity for surgery. However, collagen, a crucial component of the extracellular matrix, encountered challenges due to its limited mechanical strength and rapid in-vivo degradation. This study addresses these issues through crosslinking and functionalizing collagen with synthetic 4-arm amine-terminated polyethylene glycol (PEG) in a semi-interpenetrating network (IPN) hydrogel. The first goal is to enhance resistance to hydrolysis, thus extending the biodegradation rate. Then, to explore its electrical conductivity properties for certain applications like neural tissue regeneration. The hydrogels were fabricated using sequential IPN formation synthesis where their structural stability and type of degradation by-products were confirmed using Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, scanning electron microscopy (SEM), and nuclear magnetic resonance (NMR). Next, its mechanical and degradation properties investigations exhibit a 92% enhancement in hardness and a 90% retainment of its initial mass over time under physiological conditions. Additionally, the introduction of polypyrrole (PPy) via in-situ polymerization increases its electrical conductivity, achieving a remarkable 104-fold increase at a 0.75 M concentration, attributed to the interconnectivity of PPy chain networks within the three-dimensional structure of IPN collagen/PEG hydrogel. The increased PPy concentration improves conductivity and reduces energy requirements for redox reactions, ensuring electrochemical stability as revealed by cyclic voltammetry analysis. The demonstrated structural and electrochemical stability of the semi-IPN collagen/PEG/PPy hydrogel within a physiological environment through a facile sequential crosslinking method underscores its promising practical applications in enhancing clinical effectiveness.
publisher WILEY
issn 1042-7147
1099-1581
publishDate 2024
container_volume 35
container_issue 8
doi_str_mv 10.1002/pat.6546
topic Polymer Science
topic_facet Polymer Science
accesstype
id WOS:001290844200001
url https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001290844200001
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collection Web of Science (WoS)
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