School of Science, Faculty of Engineering and Science, University of Greenwich at Medway, Central Avenue, Chatham Maritime, Kent ME4 4TB, UK.
School of Science, Faculty of Engineering and Science, University of Greenwich at Medway, Central Avenue, Chatham Maritime, Kent ME4 4TB, UK.
Int J Pharm. 2019 Apr 5;560:406-415. doi: 10.1016/j.ijpharm.2019.02.020. Epub 2019 Feb 21.
Recently, various additive manufacturing (3D printing) approaches have been employed to fabricate dressings such as film scaffolds that possess well defined architecture and orientation at the micro level. In this study, crosslinked chitosan (CH) based film matrices were prepared using 3D printing with genipin (GE) as a crosslinker, with glycerol (GLY) and poly ethylene glycol (PEG) as plasticizer. The 3D printed films were functionally characterized using (tensile, fluid handling, mucoadhesion, drug dissolution, morphological properties and cell viability as well physico-chemical characterization using scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray diffraction. CH-GE-PEG600 3D printed films having the ratio of 1:1 polymer: plasticizer was selected due to their appropriate flexibility. Fourier transform infrared results showed intermolecular interaction between CH, GE and PEG which was confirmed by X-ray diffraction showing amorphous matrix structure. In vitro mucoadhesion studies of CH-GE-PEG600 films showed the capability of the 3D printed film to adhere to the epithelial surface. Scanning electron microscopy images showed that the surface of the plasticised films were smooth indicating content uniformity of CH, GE and PEG whilst micro cracks in unplasticised films confirmed their brittle nature. Plasticised films also showed high swelling capacity which enhanced water absorption. Cytotoxicity (MTT) assay using human skin fibroblast cell lines demonstrated that more than 90% of cells were viable after 48 h confirming non-toxic nature of the 3D printed CH-GE-PEG600 films and therefore promising dressing for chronic wound healing applications.
最近,各种增材制造(3D 打印)方法已被用于制造敷料,如具有微观水平上明确结构和取向的薄膜支架。在这项研究中,使用京尼平(GE)作为交联剂,甘油(GLY)和聚乙二醇(PEG)作为增塑剂,通过 3D 打印制备交联壳聚糖(CH)基薄膜基质。使用(拉伸、流体处理、粘膜粘附、药物溶解、形态特性和细胞活力)以及扫描电子显微镜、傅里叶变换红外光谱和 X 射线衍射等物理化学特性来对 3D 打印膜进行功能表征。由于其适当的柔韧性,选择了聚合物:增塑剂比为 1:1 的 CH-GE-PEG600 3D 打印膜。傅里叶变换红外结果表明 CH、GE 和 PEG 之间存在分子间相互作用,X 射线衍射证实了无定形基质结构。CH-GE-PEG600 膜的体外粘膜粘附研究表明 3D 打印膜能够粘附在上皮表面。扫描电子显微镜图像显示,增塑膜的表面光滑,表明 CH、GE 和 PEG 的含量均匀,而未增塑膜中的微裂纹证实了其脆性。增塑膜还显示出高溶胀能力,增强了吸水性。使用人皮肤成纤维细胞系进行的细胞毒性(MTT)测定表明,48 小时后超过 90%的细胞存活,证实了 3D 打印 CH-GE-PEG600 膜的无毒性质,因此有望用于慢性伤口愈合应用。