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受 Tunichrome 启发的没食子酚功能化壳聚糖用于组织黏附和止血。

Tunichrome-inspired pyrogallol functionalized chitosan for tissue adhesion and hemostasis.

机构信息

Division of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.

Institute of Environmental and Energy Technology, Pohang University of Science and Technology, Pohang 37673, Republic of Korea; R&D Center, ANPOLY, Inc., 77 Cheongam-ro, Pohang 37673, Republic of Korea.

出版信息

Carbohydr Polym. 2019 Mar 15;208:77-85. doi: 10.1016/j.carbpol.2018.12.017. Epub 2018 Dec 21.

Abstract

The nature-inspired fabrication of tissue adhesive and hemostatic hydrogels holds great potential for restoring damaged internal tissue in regenerative medicine. However, feeble adhesion, multifaceted systems, prohibitive costs, and toxicity impede their applications in the medical field. In order to solve this problem, we fabricated chitosan-based wet tissue adhesive with hemostatic functions inspired by the self-healing mechanism of the tunicate. In order to introduce pyrogallol moiety, gallic acids, which are broadly distributed in nature, were incorporated into chitosan backbone, a key residue for the self-healing process of tunichrome in tunicates. The in vitro adhesion test results of the tunicate-inspired hydrogel exhibited two-fold greater adhesion ability in wet condition than did fibrin glue, a commercially available surgical glue. Further, the tunicate-inspired hydrogel exhibited significantly more platelet adhesion and blood clotting ability than the parent polymer. We also demonstrated the ability of the derivative to completely mimic the tunicate's fibrous structure by fabricating an electrospun mat. The hemostatic function vis-à-vis the wet adhesiveness of the synthesized chitosan-based material may be useful for facilitating the shortcomings of the restorative tissue medicine. Additionally, the electrospinning capability will enable the modulate of the structure-property relationship and a three-dimensional design for its application site.

摘要

受贻贝启发的组织粘合剂和止血水凝胶的仿生制造在再生医学中具有很大的潜力,可以恢复受损的内部组织。然而,较弱的粘附力、多方面的系统、过高的成本和毒性阻碍了它们在医学领域的应用。为了解决这个问题,我们受贻贝自修复机制的启发,制备了具有止血功能的壳聚糖基湿组织粘合剂。为了引入焦多酚部分,我们将在自然界中广泛分布的没食子酸引入壳聚糖主链中,这是贻贝中 tunichrome 自修复过程的关键残基。贻贝启发的水凝胶的体外粘附测试结果表明,在湿润条件下,其粘附能力比市售手术用纤维蛋白胶高两倍。此外,贻贝启发的水凝胶比母体聚合物表现出明显更多的血小板粘附和更强的凝血能力。我们还通过制造电纺垫来证明该衍生材料完全模仿贻贝纤维结构的能力。合成壳聚糖基材料的止血功能和湿粘性可能有助于弥补修复组织医学的不足。此外,电纺能力将能够调节结构-性能关系,并对其应用部位进行三维设计。

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