Institute of Materials Science, Max Bergmann Center of Biomaterials, TU Dresden, Budapester Str. 27, 01069, Dresden, Germany.
Biomaterials Department, INNOVENT e.V., Prüssingstr. 27B, 07745, Jena, Germany.
Macromol Biosci. 2017 Nov;17(11). doi: 10.1002/mabi.201700154. Epub 2017 Jul 6.
Innovative biomaterial-based concepts are required to improve wound healing of damaged vascularized tissues especially in elderly multimorbid patients. To develop functional hydrogels as 3D cellular microenvironments and as carrier or scavenging systems, e.g., for mediator proteins or proinflammatory factors, collagen fibrils are embedded into a network of photo-crosslinked acrylated hyaluronan (HA), chondroitin sulfate (CS), or sulfated HA (sHA). After lyophilization, the gels show a porous structure and an improved stability against degradation via hyaluronidase. Gels with CS and sHA bind significantly more lysozyme than HA/collagen gels and retard its release. The proliferation and metabolic activity of endothelial cells are significantly increased on sHA gels compared to CS- or only HA-containing hydrogels. These findings highlight the potential of HA/collagen hydrogels with sulfated glycosaminoglycans to tune the protein binding and release behavior and to directly modulate cellular response. This can be easily translated into biomimetic biomaterials with defined properties to stimulate wound healing.
需要创新的基于生物材料的概念来改善受损的血管化组织的愈合,尤其是在老年多病的患者中。为了开发功能性水凝胶作为 3D 细胞微环境以及作为载体或清除系统,例如用于介质蛋白或促炎因子,胶原纤维被嵌入到光交联的丙烯酰化透明质酸 (HA)、硫酸软骨素 (CS) 或硫酸化 HA (sHA) 的网络中。冷冻干燥后,凝胶呈现多孔结构,并通过透明质酸酶提高了对降解的稳定性。CS 和 sHA 的凝胶比 HA/胶原凝胶结合更多的溶菌酶,并减缓其释放。与仅含 CS 或 HA 的水凝胶相比,内皮细胞在 sHA 凝胶上的增殖和代谢活性显著增加。这些发现强调了含有硫酸化糖胺聚糖的 HA/胶原水凝胶在调节蛋白结合和释放行为以及直接调节细胞反应方面的潜力。这可以很容易地转化为具有定义特性的仿生生物材料,以刺激伤口愈合。