Sequentially crosslinked collagen‐based hydrogel to form a semi‐interpenetrating network for enhanced stability to hydrolytic degradation and electrochemical properties
Shahemi Nur Hidayah, Ahmad Ruzaidi Dania Adila, Ab Rahim Sharaniza, Amir Muhammad Abid, Mahat Mohd Muzamir
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引用次数: 0
Abstract
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.
期刊介绍:
Polymers for Advanced Technologies is published in response to recent significant changes in the patterns of materials research and development. Worldwide attention has been focused on the critical importance of materials in the creation of new devices and systems. It is now recognized that materials are often the limiting factor in bringing a new technical concept to fruition and that polymers are often the materials of choice in these demanding applications. A significant portion of the polymer research ongoing in the world is directly or indirectly related to the solution of complex, interdisciplinary problems whose successful resolution is necessary for achievement of broad system objectives.
Polymers for Advanced Technologies is focused to the interest of scientists and engineers from academia and industry who are participating in these new areas of polymer research and development. It is the intent of this journal to impact the polymer related advanced technologies to meet the challenge of the twenty-first century.
Polymers for Advanced Technologies aims at encouraging innovation, invention, imagination and creativity by providing a broad interdisciplinary platform for the presentation of new research and development concepts, theories and results which reflect the changing image and pace of modern polymer science and technology.
Polymers for Advanced Technologies aims at becoming the central organ of the new multi-disciplinary polymer oriented materials science of the highest scientific standards. It will publish original research papers on finished studies; communications limited to five typewritten pages plus three illustrations, containing experimental details; review articles of up to 40 pages; letters to the editor and book reviews. Review articles will normally be published by invitation. The Editor-in-Chief welcomes suggestions for reviews.