首页> 外文会议>2018 IX International Seminar of Biomedical Engineering >In vitro Biological Evaluation of Small Intestinal Submucosa - Chitosan / Hyaluronic Acid Tridimensional Scaffolds as Deep Wound Healing Dressings
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In vitro Biological Evaluation of Small Intestinal Submucosa - Chitosan / Hyaluronic Acid Tridimensional Scaffolds as Deep Wound Healing Dressings

机译:小肠粘膜下层壳聚糖/透明质酸三维支架作为深层伤口愈合敷料的体外生物学评价

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In the U.S. more than 6 million patients suffer from chronic wounds (e.g., diabetic, pressure or vascular ulcers), which represent a major public health issue and an important healthcare expenditure. Chronic deep wounds lose the ability to repair without the external signals responsible for enhancing extracellular matrix (ECM) restoration and promoting sustained healing. We have previously prepared Small Intestinal Submucosa-Chitosan (SIS-Ch) and Small Intestinal SubmucosaHyaluronic Acid (SIS-HA) 3D scaffolds, in the form of porous sponges and hydrogels. Physicochemical and mechanical properties in vitro confirmed their potential as wound dressings. Here we conducted in vitro biological tests of SIS-Ch (n=3) and SIS-HA (n=3) scaffolds that included MTT assays to determined cytotoxicity and hemolysis assay to assess the tendency to damage red blood cells. Cell viability of SIS-Ch and SIS-HA sponges exceeded 80%. Nevertheless, SIS-HA hydrogels exhibited the greatest cell viability values of all formulations most likely due to the HA natural function in extracellular matrix that promotes cell migration and proliferation. The presence of Ch and HA in the scaffolds correlated with higher cell metabolic rates when compared with formulations based on SIS only (p<0.05). Hemolytic indexes below 5% were found for all formulations except for SIS_Ch Low and SIS_HA High for porous sponges, confirming thereby their limited tendency to promote hemolysis. Our in vitro biological findings suggest that both SIS-Ch and SISHA scaffolds have the characteristics to be evaluated in preclinical in vivo testing.
机译:在美国,超过600万患者患有慢性伤口(例如糖尿病,压力性或血管性溃疡),这代表着主要的公共卫生问题和重要的医疗保健支出。慢性深层伤口在没有负责增强细胞外基质(ECM)恢复并促进持续愈合的外部信号的情况下失去了修复能力。我们之前已经准备了多孔海绵和水凝胶形式的小肠粘膜下壳聚糖(SIS-Ch)和小肠粘膜下透明质酸(SIS-HA)3D支架。体外的物理化学和机械性能证实了其作为伤口敷料的潜力。在这里,我们进行了SIS-Ch(n = 3)和SIS-HA(n = 3)支架的体外生物学测试,其中包括MTT测定以确定细胞毒性和溶血测定,以评估破坏红细胞的趋势。 SIS-Ch和SIS-HA海绵的细胞活力超过80%。尽管如此,SIS-HA水凝胶在所有制剂中仍显示出最大的细胞活力值,这很可能是由于细胞外基质中的HA天然功能促进了细胞迁移和增殖。与仅基于SIS的制剂相比,支架中Ch和HA的存在与更高的细胞代谢率相关(p <0.05)。除多孔海绵的SIS_Ch Low和SIS_HA High外,所有制剂的溶血指数均低于5%,从而证实了它们促进溶血的趋势有限。我们的体外生物学发现表明,SIS-Ch和SISHA支架均具有在临床前体内测试中需要评估的特征。

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