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可注射的胺功能化石墨烯和硫酸软骨素水凝胶,具有软骨再生的潜力。

Injectable amine functionalized graphene and chondroitin sulfate hydrogel with potential for cartilage regeneration.

机构信息

Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, USA.

出版信息

J Mater Chem B. 2019 Apr 21;7(15):2442-2453. doi: 10.1039/c8tb02967a. Epub 2019 Mar 13.

Abstract

Damaged cartilage does not readily heal and often requires surgical intervention that only modestly improves outcomes. A synthetic material that could be injected and covalently crosslinked in situ to form a bioactive, mechanically robust scaffold that promotes stem cell chondrogenic differentiation holds promise for next-generation treatment of cartilage lesions. Here, Johnson-Claisen rearrangement chemistry was performed on graphene oxide (GO) to enable functionalization with a primary amine covalently bound to the graphenic backbone through a chemically stable linker. The primary amines are used to form covalent crosslinks with chondroitin sulfate, an important component of cartilage that promotes regeneration, to form a hydrogel (EDAG-CS). The EDAG-CS system gels in situ within 10 min, and the graphenic component imparts improved mechanical properties, including stiffness (320% increase) and toughness (70% increase). EDAG-CS hydrogels are highly porous, resistant to degradation, and enable the growth of human mesenchymal stem cells and their deposition of collagen matrix. This system has potential to improve clinical outcomes of patients with cartilage damage.

摘要

受损的软骨不易自行修复,通常需要手术干预,但这种方法只能适度改善效果。有一种合成材料,可以注射到体内,并通过原位共价交联形成一种具有生物活性且机械强度高的支架,促进干细胞软骨分化,有望成为下一代软骨损伤治疗方法。在此,通过 Johnson-Claisen 重排反应对氧化石墨烯(GO)进行修饰,使其通过化学稳定的连接子与石墨主链上的伯胺共价结合,实现功能化。伯胺与软骨素硫酸盐(一种促进再生的软骨重要成分)形成共价交联,形成水凝胶(EDAG-CS)。EDAG-CS 系统在 10 分钟内原位凝胶化,而石墨成分赋予其更高的机械性能,包括硬度(增加 320%)和韧性(增加 70%)。EDAG-CS 水凝胶具有高多孔性、抗降解性,并能促进人骨髓间充质干细胞的生长及其胶原蛋白基质的沉积。该系统有可能改善软骨损伤患者的临床效果。

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