'Materials+Technologies' Group, Department of Chemical and Environmental Engineering, Polytechnic School, University of the Basque Country, Plaza Europa 1, 20018 Donostia-San Sebastián, Spain.
Carbohydr Polym. 2016 Sep 20;149:94-101. doi: 10.1016/j.carbpol.2016.04.091. Epub 2016 Apr 23.
This article deals with the preparation of bionanocomposite hydrogels from natural polymers and nanoentities, an emerging class of materials for biotechnological and biomedical applications. Herein, the applicability of the Diels-Alder "click" reaction to the design of bionanocomposite hydrogels from furan modified gelatin using maleimide-functionalized cellulose nanocrystals as multifunctional cocross-linkers is demonstrated. The functionalization of cellulose nanocrystals with maleimide moieties was confirmed by XPS. The swelling and rheological properties of the resulting bionanocomposite confirmed the formation of hydrogel networks with covalently embedded nanoentities. The Diels-Alder reaction resulted in the formation of stiffer networks with lower swelling ratios due to the formation of additional cross-linking points. The designed "click" strategy proved to be a promising candidate for the formation of fully renewable bionanocomposite hydrogels.
本文涉及从天然聚合物和纳米实体制备生物纳米复合水凝胶,这是一类新兴的用于生物技术和生物医学应用的材料。本文展示了使用马来酰亚胺功能化的纤维素纳米晶体作为多功能共交联剂,通过 Diels-Alder“点击”反应设计呋喃改性明胶基生物纳米复合水凝胶的适用性。通过 XPS 确认了纤维素纳米晶体的马来酰亚胺基的功能化。所得生物纳米复合水凝胶的溶胀和流变性能证实了具有共价嵌入纳米实体的水凝胶网络的形成。由于形成了额外的交联点,Diels-Alder 反应导致形成更硬的网络和更低的溶胀比。所设计的“点击”策略被证明是形成完全可再生生物纳米复合水凝胶的有前途的候选方案。