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