Biochemistry and Biotechnology Laboratory, Central Leather Research Institute, Council of Scientific and Industrial Research (CSIR), Adyar, Chennai 600020, India; Academy of Scientific and Innovative Research (AcSIR), CSIR-CLRI Campus, Chennai 600020, India.
Biochemistry and Biotechnology Laboratory, Central Leather Research Institute, Council of Scientific and Industrial Research (CSIR), Adyar, Chennai 600020, India.
Int J Biol Macromol. 2020 Dec 15;165(Pt A):930-947. doi: 10.1016/j.ijbiomac.2020.09.212. Epub 2020 Oct 2.
The present study explores the curative efficacy of collagen-fibrin scaffold with Gallic acid loaded Chitosan nanoparticles (GA-CSNPs) in wound healing. GA-CSNPs were synthesized by ionotropic gelation and the incorporation of GA was confirmed with Fourier Transform Infra-Red Spectroscopy (FTIR). Change in the crystal structure of GA was confirmed by X-ray Powder Diffraction (X-PRD) and Differential Scanning Colorimetry (DSC). Surface Electron microscopy (SEM) showed that GA-CSNPs have roughly spherical morphology and mean diameter of 251.3 nm with positive zeta potential. The drug encapsulation was found to be 34.2-73.5%. Col-fibrin scaffolds crosslinked with genipin using cryodesiccation technique showed a sheet-like architecture with 66.78% of crosslinking degree. Scaffolds exhibited porosity of 38.49% and decrease in swelling ratio. Biodegradation study demonstrated controlled degradation with collagenase and Thermogravimetric analysis (TGA) showed excellent thermal stability and sustained drug release property. In vitro and in vivo study results indicate that the group treated with nanocomposite scaffold exhibits enhanced re-epithelialization, accelerated fibroblast cell migration, wound healing and significant wound contraction (p < 0.001) compared to control. Nanocomposite scaffolds also accelerates angiogenesis, hexosamine synthesis, collagen deposition and recruiting immune cells at wound area. These results suggest nanocomposite scaffold values for their use as a promising wound dressing material for better tissue regeneration.
本研究探讨了载没食子酸壳聚糖纳米粒子(GA-CSNPs)的胶原纤维支架在伤口愈合中的治疗效果。GA-CSNPs 通过离子凝胶化合成,并通过傅里叶变换红外光谱(FTIR)证实了 GA 的掺入。GA 晶体结构的变化通过 X 射线粉末衍射(X-PRD)和差示扫描量热法(DSC)得到证实。表面电子显微镜(SEM)显示,GA-CSNPs 具有大致球形的形态,平均直径为 251.3nm,具有正的 Zeta 电位。药物包封率为 34.2-73.5%。使用冷冻干燥技术用京尼平交联的 Col-fibrin 支架呈现片状结构,交联度为 66.78%。支架的孔隙率为 38.49%,溶胀比降低。降解研究表明胶原酶具有可控的降解性,热重分析(TGA)表明具有优异的热稳定性和持续的药物释放性能。体外和体内研究结果表明,与对照组相比,纳米复合支架治疗组表现出增强的再上皮化、加速的成纤维细胞迁移、伤口愈合和显著的伤口收缩(p<0.001)。纳米复合支架还能促进血管生成、己糖胺合成、胶原沉积和在伤口部位募集免疫细胞。这些结果表明,纳米复合支架具有作为有前途的伤口敷料材料的价值,可实现更好的组织再生。