Mahmoud Azza A, Salama Alaa H
Department of Pharmaceutical Technology, National Research Center, Dokki, Cairo, Egypt; Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt, Cairo, Egypt.
Department of Pharmaceutical Technology, National Research Center, Dokki, Cairo, Egypt.
Eur J Pharm Sci. 2016 Feb 15;83:155-65. doi: 10.1016/j.ejps.2015.12.026. Epub 2015 Dec 28.
Biomaterial scaffolds are versatile tools as drug carrier for treatment of wounds. A series of norfloxacin-loaded scaffolds were synthesized for treatment of wounds by combining collagen with two different types of chitosan using freeze-drying technique. Subsequently, scaffolds were screened in terms of morphology, water absorption and retention capacity, biodegradation, ex-vivo bioadhesive strength, in-vitro drug release biological compatibility, X-ray diffractometry, differential scanning calorimetry as well as in-vivo evaluation. The results indicate that the scaffold mechanical strength is dependent on the type of used chitosan. The prepared scaffolds contained interconnected porous architecture. The scaffolds had high water uptake and retention capacity with extended biodegradation rate. Scaffolds prepared with chitosan HCl showed superior bioadhesive strength compared to those prepared with low molecular weight chitosan. All scaffolds showed almost 100% drug release within 24h. As identified by the terahertz pulsed imaging measurements, there is single scaffold area with the same concentration. After 28 days of wound dressing with selected norfoloxacin-loaded or unloaded collagen/chitosan scaffolds in Albino rats, it was found that the tissue regeneration time was fast compared to non-treated wounds. Furthermore, the drug-loaded scaffolds showed normal structure of an intact epidermal layer as well as the underlying dermis as revealed by histopathological studies. The obtained results suggest that the investigated norfloxacin-loaded collagen/chitosan scaffold is a potential candidate for skin regeneration application.
生物材料支架作为用于伤口治疗的药物载体是多功能工具。采用冷冻干燥技术,将胶原蛋白与两种不同类型的壳聚糖结合,合成了一系列负载诺氟沙星的支架用于伤口治疗。随后,从形态、吸水和保水能力、生物降解、体外生物粘附强度、体外药物释放、生物相容性、X射线衍射、差示扫描量热法以及体内评估等方面对支架进行筛选。结果表明,支架的机械强度取决于所用壳聚糖的类型。制备的支架具有相互连接的多孔结构。支架具有高吸水性和保水能力以及延长的生物降解率。与用低分子量壳聚糖制备的支架相比,用盐酸壳聚糖制备的支架表现出优异的生物粘附强度。所有支架在24小时内几乎释放100%的药物。通过太赫兹脉冲成像测量确定,存在单个具有相同浓度的支架区域。在用选定的负载或未负载诺氟沙星的胶原蛋白/壳聚糖支架对白化大鼠进行伤口敷料28天后,发现与未治疗的伤口相比,组织再生时间更快。此外,组织病理学研究表明,载药支架显示出完整表皮层以及下层真皮的正常结构。所得结果表明,所研究的负载诺氟沙星的胶原蛋白/壳聚糖支架是皮肤再生应用的潜在候选者。