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硼酸和藻酸盐之间的动态键合:具有拉伸、自修复、刺激响应、可重塑和粘附性能的水凝胶。

Dynamic Bonds between Boronic Acid and Alginate: Hydrogels with Stretchable, Self-Healing, Stimuli-Responsive, Remoldable, and Adhesive Properties.

机构信息

Department of Chemistry , Korea Advanced Institute of Science and Technology (KAIST) , 291 Daehak-ro , Yuseong-gu, Daejeon , 305-701 , South Korea.

R&D Center InnoTherapy Inc. 25, Sonyou 13th Rd, High-tech CityII Suite #2019 , Youngdeungpo-Gu 07282 , South Korea.

出版信息

Biomacromolecules. 2018 Jun 11;19(6):2053-2061. doi: 10.1021/acs.biomac.8b00144. Epub 2018 Apr 11.

Abstract

For the increasing demand of soft materials with wide ranges of applications, hydrogels have been developed exhibiting variety of functions (e.g., stretchable, self-healing, stimuli-responsive, and etc.). So far, add-in components such as inorganic nanoparticles, carbon materials, clays, and many others to main polymers have been used to achieve various unique functions of hydrogels. The multicomponent hydrogel systems often exhibit batch-dependent inconsistent results and problems in multicomponent mixings, require labors during preparations, and accompany unpredictable cross-talk between the added components. Here, we developed 'single polymeric component', alginate-boronic acid (alginate-BA) hydrogel to overcome the aforementioned problems. It exhibits unprecedented multifunctionalities simultaneously, such as high stretchability, self-healing, shear-thinning, pH- and glucose-sensitivities, adhesive properties, and reshaping properties. Multifunctionalities of alginate-BA hydrogel is resulted from the reversible inter- and intramolecular interactions by dynamic equilibrium of boronic acid-diol complexation and dissociation, which was proved by single molecule level Atomic Force Microscopy (AFM) pulling experiments. We also found that the alginate-BA gel showed enhanced in vivo retentions along gastrointestinal (GI) tract. Our findings suggest that rational polymer designs can result in minimizing the number of a participating component for multifunctional hydrogels, instead of increasing complexity by adding various additional components.

摘要

为满足对具有广泛应用的软材料日益增长的需求,已经开发出了具有多种功能(例如可拉伸、自修复、刺激响应等)的水凝胶。迄今为止,已经向主聚合物中添加了诸如无机纳米粒子、碳材料、粘土等多种添加剂,以实现水凝胶的各种独特功能。多组分水凝胶体系通常表现出批次依赖性的不一致结果和多组分混合问题,在制备过程中需要耗费人力,并且添加的成分之间存在不可预测的串扰。在这里,我们开发了“单一聚合物组分”藻酸盐-硼酸(alginate-BA)水凝胶来克服上述问题。它同时表现出前所未有的多功能性,例如高拉伸性、自修复、剪切稀化、pH 和葡萄糖敏感性、粘附性和可重塑性。藻酸盐-BA 水凝胶的多功能性源于硼酸-二醇配合物的动态平衡所产生的分子内和分子间的可逆相互作用,这通过单分子水平原子力显微镜(AFM)拉伸实验得到了证明。我们还发现,藻酸盐-BA 凝胶在胃肠道(GI)中显示出增强的体内保留性。我们的研究结果表明,合理的聚合物设计可以减少参与多功能水凝胶的组分数量,而不是通过添加各种附加组分来增加复杂性。

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