Departamento de Química Orgánica, Facultad de Ciencias Químicas (Universidad Nacional de Córdoba), IPQA-CONICET, Haya de la Torre y Medina Allende, Córdoba X5000HUA, Argentina.
Instituto de Física del Litoral (IFIS-Litoral, CONICET-UNL), Güemes 3450, Santa Fe 3000, Argentina.
ACS Biomater Sci Eng. 2022 Nov 14;8(11):5027-5037. doi: 10.1021/acsbiomaterials.2c00935. Epub 2022 Nov 1.
The design of ultratough hydrogels has recently emerged as a topic of great interest in the scientific community due to their ability to mimic the features of biological tissues. An outstanding strategy for preparing these materials relies on reversible and dynamic cross-links within the hydrogel matrix. In this work, inspired by the composition of ascidians' tunic, stretchable supramolecular hydrogels combining poly(vinyl alcohol), green tea-derived gallic acid, and rigid tannic acid-coated cellulose nanocrystals (TA@CNC) were designed. The addition of TA@CNC nanofillers in concentrations up to 1.2 wt % significantly impacted the mechanical and viscoelastic properties of the hydrogels due to the promotion of hydrogen bonding with the polymer matrix and polyphenols π-π stacking interactions. These supramolecular associations endow the hydrogels with excellent stretchability and strength (>340%, 540 kPa), low thermoreversible gel-sol transition (60 °C), and remolding ability, while the natural polyphenols provided potential antibacterial properties. These versatile materials can be anticipated to open up new prospects for the rational design of polyphenol-based cellulosic hydrogels for different biomedical applications.
由于能够模拟生物组织的特性,超坚韧水凝胶的设计最近成为科学界关注的焦点。制备这些材料的一种杰出策略是在水凝胶基质中使用可逆和动态的交联。在这项工作中,受藤壶外膜组成的启发,设计了一种可拉伸的超分子水凝胶,该水凝胶结合了聚乙烯醇、绿茶衍生的没食子酸和刚性单宁酸涂覆的纤维素纳米晶体(TA@CNC)。由于与聚合物基质和多酚π-π 堆积相互作用促进氢键形成,TA@CNC 纳米填料在高达 1.2wt%的浓度下加入时,会显著影响水凝胶的力学和粘弹性性能。这些超分子缔合赋予水凝胶优异的拉伸性和强度(>340%,540kPa)、较低的热可逆凝胶-溶胶转变(60°C)和重塑能力,同时天然多酚提供了潜在的抗菌性能。这些多功能材料有望为不同的生物医学应用中基于多酚的纤维素水凝胶的合理设计开辟新的前景。