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儿茶酚化羟乙基壳聚糖的交联作为组织黏合剂。

-stimulated crosslinking of catechol-conjugated hydroxyethyl chitosan as a tissue adhesive.

机构信息

College of Marine Life Sciences, Ocean University of China, Qingdao, China.

Department of Chemistry and Chemical Biology, Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, New York, 12180.

出版信息

J Biomed Mater Res B Appl Biomater. 2019 Apr;107(3):582-593. doi: 10.1002/jbm.b.34150. Epub 2018 May 7.

DOI:10.1002/jbm.b.34150
PMID:29732734
Abstract

Catechol-functionalized polymers are of particular interest because of their strong water-resistant adhesive properties. Hydroxymethyl chitosan (HECTS) has been used as an implantable biomaterial having good water solubility, biodegradability and biocompatibility. Here, hydrocaffeic acid (HCA) grafted HECTS (HCA-g-HECTS) was prepared through carbodiimide coupling and the tethered catechol underwent periodate ( )-stimulated mono and double cross-linking with genipin. The gelation time of these cross-linked HCA-g-HECTS hydrogels decreased with increasing molar ratio of cross-linker to grafted catechol group, increasing temperature, or the addition of genipin. Under the same molar ratio of cross-linker to catechol, -induced cross-linked HCA-g-HECTS hydrogels exhibited much stronger storage modulus and temperature stability than hydrogels made by Fe -triggered cross-linking. The -stimulated HCA-g-HECTS hydrogels were biocompatible on a cellular level when the molar ratio of to catechol group was less than 0.5:1. The hydrogels prepared with a 0.125:1 molar ratio of to catechol group exhibited high adhesion strength of 73.56 kPa against wet rat skin, and a higher adhesion strength than sutures in a rat wound closure model. This biocompatible -stimulated HCA-g-HECTS hydrogel may represent a promising new tissue adhesive. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2018. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B: 582-593, 2019.

摘要

儿茶酚功能化聚合物因其强耐水粘合性能而受到特别关注。羟甲基壳聚糖(HECTS)已被用作具有良好水溶性、生物可降解性和生物相容性的可植入生物材料。在此,通过碳二亚胺偶联制备了咖啡酸(HCA)接枝羟甲基壳聚糖(HCA-g-HECTS),并且接枝的儿茶酚在高碘酸钠( )刺激下发生单和双交联反应,与京尼平交联。这些交联 HCA-g-HECTS 水凝胶的凝胶时间随着交联剂与接枝儿茶酚基团的摩尔比、温度升高或京尼平的添加而降低。在相同的交联剂与儿茶酚摩尔比下, 诱导交联的 HCA-g-HECTS 水凝胶表现出比 Fe 3+ 引发交联的水凝胶更强的储能模量和温度稳定性。当 与儿茶酚基团的摩尔比小于 0.5:1 时, 诱导的 HCA-g-HECTS 水凝胶在细胞水平上具有生物相容性。当 与儿茶酚基团的摩尔比为 0.125:1 时,水凝胶表现出对湿大鼠皮肤的高粘合强度为 73.56 kPa,并且在大鼠伤口闭合模型中比缝线具有更高的粘合强度。这种生物相容的 诱导的 HCA-g-HECTS 水凝胶可能代表一种有前途的新型组织粘合剂。© 2018 年 Wiley 期刊,Inc. J 生物医学材料研究杂志 B:应用生物材料,2018. © 2018 年 Wiley 期刊,Inc. J 生物医学材料研究杂志 B:应用生物材料 107B:582-593,2019.

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