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基于自催化 Fe/没食子酸-纤维素纳米纤维的多功能水凝胶/复合材料的超快凝胶化。

Ultrafast gelation of multifunctional hydrogel/composite based on self-catalytic Fe/Tannic acid-cellulose nanofibers.

机构信息

Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi, People's Republic of China.

Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi, People's Republic of China.

出版信息

J Colloid Interface Sci. 2022 Jan 15;606(Pt 2):1457-1468. doi: 10.1016/j.jcis.2021.08.104. Epub 2021 Aug 18.

Abstract

Multifunctional hydrogels with transparency, ultraviolet (UV)-blocking, stretchable, self-healing, adhesive, antioxidant and antibacterial properties are promising materials for biomedical and relevant applications. However, preparation of these hydrogels at ambient environment without stimuli is still a challenge. Here, a series of hydrogels possessing ultrashort gelation time (~30 s) at room or cold temperature were fabricated based on self-catalytic Fe/Tannic acid-cellulose nanofiber (Fe/TA-CNF). Fe/TA-CNF formed stable redox pairs to activate ammonium persulfate (initiator), generating abundant free radicals to trigger the ultrafast polymerization of acrylic acid (AA). To improve the antibacterial ability of hydrogel, a bilayer hydrogel composite (NF@HG) composed of tetracycline hydrochloride (TH)-loaded electrospun nanofibers and hydrogel layer was fabricated via a mild casting method. The NF@HG exhibited enhanced antibacterial ability and the sustained release of TH can provide long-term antibacterial activity. Besides, cell viability results demonstrated that NF@HG was non-cytotoxic. Taken together, this strategy based on self-catalytic Fe/TA-CNF system may inspire new aspects on fast and economical preparation of multifunctional hydrogels or composites, which have attractive industrial applications for biomedical materials.

摘要

具有透明度、紫外线(UV)阻断、拉伸、自修复、粘附、抗氧化和抗菌性能的多功能水凝胶是生物医学和相关应用的有前途的材料。然而,在环境温度下无需刺激即可制备这些水凝胶仍然是一个挑战。在这里,基于自催化的 Fe/没食子酸-纤维素纳米纤维(Fe/TA-CNF),制备了一系列在室温或低温下具有超短凝胶化时间(~30 s)的水凝胶。Fe/TA-CNF 形成稳定的氧化还原对来激活过硫酸铵(引发剂),产生丰富的自由基来引发丙烯酸(AA)的超快聚合。为了提高水凝胶的抗菌能力,通过温和的铸造方法制备了由盐酸四环素(TH)负载的静电纺纳米纤维和水凝胶层组成的双层水凝胶复合材料(NF@HG)。NF@HG 表现出增强的抗菌能力,并且 TH 的持续释放可以提供长期的抗菌活性。此外,细胞活力结果表明 NF@HG 无细胞毒性。总之,这种基于自催化 Fe/TA-CNF 体系的策略可能会激发快速、经济地制备多功能水凝胶或复合材料的新方面,这对生物医学材料具有有吸引力的工业应用。

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