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GAGs-thiolated chitosan assemblies for chronic wounds treatment: control of enzyme activity and cell attachment

机译:用于慢性伤口治疗的GAGs硫醇化壳聚糖组装体:酶活性和细胞附着的控制

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摘要

Multilayered polyelectrolyte coatings comprising thiolated chitosan (TC) and glycosaminoglycans (GAGs), chondroitin sulphate and hyaluronic acid, were built using a layer-by-layer approach. The surface activity of these coatings for binding and inhibition of enzymes related to chronic inflammation, such as collagenase and myeloperoxidase, was assessed. The build-up of five bi-layers of TC/GAGs onto gold surfaces was monitored in situ by QCM-D. All experimental groups showed exponential growth of the coatings controlled by the degree of chitosan thiolation and the molecular weight of the GAGs. The degree of chitosan modification was also the key parameter influencing the enzyme activity: increasing the thiols content led to more efficient myeloperoxidase inhibition and was inversely proportional to the adsorption of collagenase. Enhanced fibroblast attachment and proliferation were observed when the multilayered polyelectrolyte constructs terminated with GAGs. The possibility to control either the activity of major wound enzymes by the thiolation degree of the coating or the cell adhesion and proliferation by proper selection of the ultimate layer makes these materials potentially useful in chronic wounds treatment and dermal tissue regeneration.
机译:使用逐层方法构建包含硫醇化壳聚糖(TC)和糖胺聚糖(GAG),硫酸软骨素和透明质酸的多层聚电解质涂层。评估了这些涂层对结合和抑制与慢性炎症相关的酶(如胶原酶和髓过氧化物酶)的表面活性。通过QCM-D在原位监测金表面上五个双层TC / GAG的堆积。所有实验组均显示出壳聚糖硫醇化程度和GAG分子量控制的涂层指数增长。壳聚糖修饰的程度也是影响酶活性的关键参数:增加硫醇含量导致更有效的髓过氧化物酶抑制作用,并且与胶原酶的吸附成反比。当多层聚电解质构建体以GAGs终止时,观察到增强的成纤维细胞附着和增殖。通过涂布或通过最终层的适当选择的细胞粘附和增殖的硫醇化程度,以控制主要伤口的酶的任一活性的可能性使得在慢性创伤的治疗和真皮组织再生潜在有用的这些材料。

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