A lignin-based controlled/sustained release hydrogel by integrating mechanical strengthening and bioactivities of lignin

IF 20.2 Q1 MATERIALS SCIENCE, PAPER & WOOD
Bowei Wang, Dingkun Qiu, Yihui Gu, Zhu Shan, Ruonan Shi, Jing Luo, Shuang Qi, Yilin Wang, Bo Jiang, Yongcan Jin
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Abstract

The favorable antioxidant and antimicrobial activities of lignin have been shown to promote wound healing. However, the accumulation of lignin in high concentrations in the body brings about varying degrees of biotoxicity. Herein, a controlled/sustained release polyvinyl alcohol/chitosan/sulfonated lignin hydrogel (PVA-CS-L) integrated mechanical strengthening and bioactivities of lignin was developed. The lignin-induced non-covalent bond network (van der Waals force, hydrogen and electrostatic interactions) promoted energy dissipation when the hydrogel was subjected to stretching and compression. This endowed the PVA-CS-L hydrogel with improved tensile (∼36 kPa) and compressive strength (∼900 kPa), as well as compressive toughness (∼9.0 MJ/m3), which were superior to the polyvinyl alcohol/chitosan hydrogel (PVA-CS) (31 kPa, 680 kPa, and 7.5 MJ/m3, respectively). The construction of electrostatic interaction could not only slow down the sudden release of lignin but also make the hydrogel exhibit a good pH-sensitive behavior of controlled-release lignin. Also, the developed hydrogel had good biocompatibility and the released lignin had reactive oxygen species scavenging as well as inhibitory activity against Staphylococcus aureus. Finally, preliminary evaluation of drug delivery reveals that the presence of lignin enabled the hydrogel to exhibit longer-lasting controlled/sustained epigallocatechin gallate release properties. Such lignin-based controlled/sustained release hydrogel that integrates the molecular structure and biological difunctional features of lignin gives new insight into cost-effective, easy-to-operate manufacturing of load-bearing and bioactive materials.
一种结合木质素机械强化和生物活性的木质素控制/缓释水凝胶
木质素具有良好的抗氧化和抗菌活性,可促进伤口愈合。然而,高浓度木质素在体内的积累会带来不同程度的生物毒性。本文研究了一种集机械强化和木质素生物活性于一体的聚乙烯醇/壳聚糖/磺化木质素水凝胶(PVA-CS-L)。木质素诱导的非共价键网络(范德华力、氢和静电相互作用)促进了水凝胶在拉伸和压缩时的能量耗散。这使得PVA-CS- l水凝胶具有更高的拉伸强度(~ 36 kPa)和抗压强度(~ 900 kPa),以及抗压韧性(~ 9.0 MJ/m3),优于聚乙烯醇/壳聚糖水凝胶(PVA-CS)(分别为31 kPa, 680 kPa和7.5 MJ/m3)。静电相互作用的构建不仅可以减缓木质素的突然释放,而且使水凝胶表现出良好的控释木质素的ph敏感行为。制备的水凝胶具有良好的生物相容性,释放的木质素具有清除活性氧和抑制金黄色葡萄球菌的活性。最后,药物传递的初步评估表明木质素的存在使水凝胶表现出更持久的控制/持续的表没食子儿茶素没食子酸酯释放特性。这种基于木质素的控制/缓释水凝胶结合了木质素的分子结构和生物双功能特征,为成本效益高,易于操作的承重和生物活性材料制造提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bioresources and Bioproducts
Journal of Bioresources and Bioproducts Agricultural and Biological Sciences-Forestry
CiteScore
39.30
自引率
0.00%
发文量
38
审稿时长
12 weeks
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