Tannic Acid-Induced Gelation of Aqueous Suspensions of Cellulose Nanocrystals

Nanocellulose hydrogels are a crucial category of soft biomaterials with versatile applications in tissue engineering, artificial extracellular matrices, and drug-delivery systems. In the present work, a simple and novel method, involving the self-assembly of cellulose nanocrystals (CNCs) induced by...

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Main Authors: Fengcai Lin, Wenyan Lin, Jingwen Chen, Chenyi Sun, Xiaoxiao Zheng, Yanlian Xu, Beili Lu, Jipeng Chen, Biao Huang
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:Polymers
Subjects:
Online Access:https://www.mdpi.com/2073-4360/15/20/4092
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author Fengcai Lin
Wenyan Lin
Jingwen Chen
Chenyi Sun
Xiaoxiao Zheng
Yanlian Xu
Beili Lu
Jipeng Chen
Biao Huang
author_facet Fengcai Lin
Wenyan Lin
Jingwen Chen
Chenyi Sun
Xiaoxiao Zheng
Yanlian Xu
Beili Lu
Jipeng Chen
Biao Huang
author_sort Fengcai Lin
collection DOAJ
description Nanocellulose hydrogels are a crucial category of soft biomaterials with versatile applications in tissue engineering, artificial extracellular matrices, and drug-delivery systems. In the present work, a simple and novel method, involving the self-assembly of cellulose nanocrystals (CNCs) induced by tannic acid (TA), was developed to construct a stable hydrogel (SH-CNC/TA) with oriented porous network structures. The gelation process is driven by the H-bonding interaction between the hydroxyl groups of CNCs and the catechol groups of TA, as substantiated by the atoms in molecules topology analysis and FTIR spectra. Interestingly, the assembled hydrogels exhibited a tunable hierarchical porous structure and mechanical moduli by varying the mass ratio of CNCs to TA. Furthermore, these hydrogels also demonstrate rapid self-healing ability due to the dynamic nature of the H-bond. Additionally, the structural stability of the SH-CNC/TA hydrogel could be further enhanced and adjusted by introducing coordination bonding between metal cations and TA. This H-bonding driven self-assembly method may promote the development of smart cellulose hydrogels with unique microstructures and properties for biomedical and other applications.
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spelling doaj.art-354cf74591a644a588102620ea6650fd2023-11-19T17:51:03ZengMDPI AGPolymers2073-43602023-10-011520409210.3390/polym15204092Tannic Acid-Induced Gelation of Aqueous Suspensions of Cellulose NanocrystalsFengcai Lin0Wenyan Lin1Jingwen Chen2Chenyi Sun3Xiaoxiao Zheng4Yanlian Xu5Beili Lu6Jipeng Chen7Biao Huang8Fujian Engineering and Research Center of New Chinese Lacquer Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, ChinaFujian Engineering and Research Center of New Chinese Lacquer Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, ChinaFujian Engineering and Research Center of New Chinese Lacquer Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, ChinaFujian Engineering and Research Center of New Chinese Lacquer Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, ChinaFujian Engineering and Research Center of New Chinese Lacquer Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, ChinaFujian Engineering and Research Center of New Chinese Lacquer Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, ChinaCollege of Material Engineering, Fujian Agriculture and Forestry University, Fuzhou 350108, ChinaFujian Engineering and Research Center of New Chinese Lacquer Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou 350108, ChinaCollege of Material Engineering, Fujian Agriculture and Forestry University, Fuzhou 350108, ChinaNanocellulose hydrogels are a crucial category of soft biomaterials with versatile applications in tissue engineering, artificial extracellular matrices, and drug-delivery systems. In the present work, a simple and novel method, involving the self-assembly of cellulose nanocrystals (CNCs) induced by tannic acid (TA), was developed to construct a stable hydrogel (SH-CNC/TA) with oriented porous network structures. The gelation process is driven by the H-bonding interaction between the hydroxyl groups of CNCs and the catechol groups of TA, as substantiated by the atoms in molecules topology analysis and FTIR spectra. Interestingly, the assembled hydrogels exhibited a tunable hierarchical porous structure and mechanical moduli by varying the mass ratio of CNCs to TA. Furthermore, these hydrogels also demonstrate rapid self-healing ability due to the dynamic nature of the H-bond. Additionally, the structural stability of the SH-CNC/TA hydrogel could be further enhanced and adjusted by introducing coordination bonding between metal cations and TA. This H-bonding driven self-assembly method may promote the development of smart cellulose hydrogels with unique microstructures and properties for biomedical and other applications.https://www.mdpi.com/2073-4360/15/20/4092cellulose nanocrystalstannic acidhydrogen bondinghydrogel
spellingShingle Fengcai Lin
Wenyan Lin
Jingwen Chen
Chenyi Sun
Xiaoxiao Zheng
Yanlian Xu
Beili Lu
Jipeng Chen
Biao Huang
Tannic Acid-Induced Gelation of Aqueous Suspensions of Cellulose Nanocrystals
Polymers
cellulose nanocrystals
tannic acid
hydrogen bonding
hydrogel
title Tannic Acid-Induced Gelation of Aqueous Suspensions of Cellulose Nanocrystals
title_full Tannic Acid-Induced Gelation of Aqueous Suspensions of Cellulose Nanocrystals
title_fullStr Tannic Acid-Induced Gelation of Aqueous Suspensions of Cellulose Nanocrystals
title_full_unstemmed Tannic Acid-Induced Gelation of Aqueous Suspensions of Cellulose Nanocrystals
title_short Tannic Acid-Induced Gelation of Aqueous Suspensions of Cellulose Nanocrystals
title_sort tannic acid induced gelation of aqueous suspensions of cellulose nanocrystals
topic cellulose nanocrystals
tannic acid
hydrogen bonding
hydrogel
url https://www.mdpi.com/2073-4360/15/20/4092
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