Afewerki Samson, Wang Xichi, Ruiz-Esparza Guillermo U, Tai Cheuk-Wai, Kong Xueying, Zhou Shengyang, Welch Ken, Huang Ping, Bengtsson Rhodel, Xu Chao, Strømme Maria
Division of Nanotechnology and Functional Materials, Department of Materials Science and Engineering, Ångström Laboratory, Uppsala University, Box 35, 751 03 Uppsala, Sweden.
Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, United States.
ACS Nano. 2020 Dec 22;14(12):17004-17017. doi: 10.1021/acsnano.0c06346. Epub 2020 Dec 11.
The engineering of multifunctional biomaterials using a facile sustainable methodology that follows the principles of green chemistry is still largely unexplored but would be very beneficial to the world. Here, the employment of catalytic reactions in combination with biomass-derived starting materials in the design of biomaterials would promote the development of eco-friendly technologies and sustainable materials. Herein, we disclose the combination of two catalytic cycles (combined catalysis) comprising oxidative decarboxylation and quinone-catechol redox catalysis for engineering lignin-based multifunctional antimicrobial hydrogels. The bioinspired design mimics the catechol chemistry employed by marine mussels in nature. The resultant multifunctional sustainable hydrogels (1) are robust and elastic, (2) have strong antimicrobial activity, (3) are adhesive to skin tissue and various other surfaces, and (4) are able to self-mend. A systematic characterization was carried out to fully elucidate and understand the facile and efficient catalytic strategy and the subsequent multifunctional materials. Electron paramagnetic resonance analysis confirmed the long-lasting quinone-catechol redox environment within the hydrogel system. Initial biocompatibility studies demonstrated the low toxicity of the hydrogels. This proof-of-concept strategy could be developed into an important technological platform for the eco-friendly, bioinspired design of other multifunctional hydrogels and their use in various biomedical and flexible electronic applications.
利用遵循绿色化学原理的简便可持续方法来设计多功能生物材料,这一领域在很大程度上仍未得到充分探索,但对世界将非常有益。在此,将催化反应与生物质衍生的起始材料相结合用于生物材料设计,将推动环保技术和可持续材料的发展。在此,我们揭示了两个催化循环(联合催化)的组合,包括氧化脱羧和醌 - 儿茶酚氧化还原催化,用于构建基于木质素的多功能抗菌水凝胶。这种受生物启发的设计模仿了自然界中海洋贻贝所采用的儿茶酚化学。所得的多功能可持续水凝胶具有以下特性:(1)坚固且有弹性;(2)具有强大的抗菌活性;(3)对皮肤组织和各种其他表面具有粘附性;(4)能够自我修复。我们进行了系统表征,以全面阐明和理解这种简便高效的催化策略以及后续的多功能材料。电子顺磁共振分析证实了水凝胶系统中持久的醌 - 儿茶酚氧化还原环境。初步的生物相容性研究表明水凝胶的毒性较低。这种概念验证策略可发展成为一个重要的技术平台,用于对其他多功能水凝胶进行环保、受生物启发的设计,并将其应用于各种生物医学和柔性电子领域。