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Preparation and Characterization of a Collagen-Liposome-Chondroitin Sulfate Matrix with Potential Application for Inflammatory Disorders Treatment

机译:胶原-脂质体-软骨素硫酸盐基质的制备与表征及其在炎症性疾病治疗中的潜在应用

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Smart drug delivery systems with controllable properties play an important role in targeted therapy and tissue regeneration. The aim of our study was the preparation andin vitroevaluation of a collagen (Col) matrix embedding a liposomal formulation of chondroitin sulfate (L-CS) for the treatment of inflammatory disorders. Structural studies using Oil Red O specific staining for lipids and scanning electron microscopy showed an alveolar network of nanosized Col fibrils decorated with deposits of L-CS at both periphery and inner of the matrix. The porosity and density of Col-L-CS matrix were similar to those of Col matrix, while its mean pore size and biodegradability had significantly higher and lower values (P<0.05), respectively.In vitrocytotoxicity assays showed that the matrix system induced high cell viability and stimulated cell metabolism in L929 fibroblast cell culture. Light and electron micrographs of the cell-matrix construct showed that cells clustered into the porous structure at 72 h of cultivation.In vitrodiffusion test indicated that the quantity of released CS was significantly lower (P<0.05) after embedment of L-CS within Col matrix. All these results indicated that the biocompatible and biodegradable Col-L-CS matrix might be a promising delivery system for local treatment of inflamed site.
机译:具有可控特性的智能药物输送系统在靶向治疗和组织再生中起着重要作用。我们研究的目的是制备并体外评估胶原蛋白(Col)基质,该基质内含硫酸软骨素(L-CS)脂质体制剂,用于治疗炎症。使用针对脂质的油红O特异性染色和扫描电子显微镜进行的结构研究表明,纳米级Col纤维的肺泡网络装饰有L-CS在基质的外围和内部的沉积物。 Col-L-CS基质的孔隙率和密度与Col基质的孔隙率和密度相似,但其平均孔径和可生物降解性分别具有较高和较低的值(P <0.05)。 L929成纤维细胞培养中的细胞活力和刺激的细胞代谢。细胞基质构建物的光和电子显微照片显示,在培养72 h时细胞聚集在多孔结构中。体外扩散试验表明,将L-CS嵌入Col中后,CS的释放量显着降低(P <0.05)。矩阵。所有这些结果表明,生物相容性和可生物降解的Col-L-CS基质可能是用于局部治疗发炎部位的有希望的递送系统。

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