Department of Pharmaceutical Technology, Faculty of Pharmacy, Beirut Arab University, Beirut, Lebanon.
Faculty of Sciences, Lebanese University, Beirut, Lebanon; Environmental Health Research Lab (EHRL), Faculty of Sciences V, Lebanese University, Nabatieh, Lebanon.
Int J Pharm. 2020 Sep 25;587:119647. doi: 10.1016/j.ijpharm.2020.119647. Epub 2020 Jul 13.
The topical delivery of nanotherapeutics at the injury site for skin regeneration has received increasing attention as a strategy for wound treatment. This study aimed to investigate the preparation of spray dried tadalafil loaded pro-nanoliposomes powder as a novel system to accelerate wound healing process. The optimization was carried out employing 3 factorial design based on phospholipid and cholesterol concentrations. The physicochemical characterizations, in vitro cellular assessment and in vivo performance were evaluated. The results obtained pointed out that phospholipid concentration presented a positive effect on the entrapment efficacy and particle size, while cholesterol hindered the entrapment efficacy yet presented a prominent influence on particle size. Moreover, the optimized formulation showed a sustained release, high zeta potential and uniform spherical particles indicating entrapment of tadalafil in its amorphous state as demonstrated by FTIR and XPRD results. Cell viability and in vitro scratch assay demonstrated no cytotoxicity on human fibroblast cell lines and the ability of the drug and optimized formulation to promote cell migration. In vivo wound healing studies revealed significantly higher wound closure rates for areas treated with optimized loaded-formulation (65.95±6.47%) compared to unloaded formulation (29.78±9.65%), free drug (38.87±11.44%) and sham group (10.22±5.11%). In the in vivo study, histopathological specimens supported the previous results with presentation of cascade of healing elements via the angiogenetic activity of tadalafil. These outcomes provide an insight of a novel and emerging therapeutic drug system for wound treatment in clinical practice.
纳米治疗剂在损伤部位的局部递送作为皮肤再生的一种策略受到越来越多的关注。本研究旨在探索喷雾干燥他达拉非载原纳米脂质体粉末的制备,作为一种加速伤口愈合过程的新系统。采用基于磷脂和胆固醇浓度的 3 因素设计进行优化。评估了物理化学特性、体外细胞评估和体内性能。结果表明,磷脂浓度对包封效率和粒径有积极影响,而胆固醇阻碍了包封效率,但对粒径有显著影响。此外,优化的配方表现出持续释放、高 Zeta 电位和均匀的球形颗粒,表明 FTIR 和 XPRD 结果表明他达拉非以无定形状态被包封。细胞活力和体外划痕试验表明,对人成纤维细胞系无细胞毒性,药物和优化配方具有促进细胞迁移的能力。体内伤口愈合研究表明,与未加载配方(29.78±9.65%)、游离药物(38.87±11.44%)和假手术组(10.22±5.11%)相比,经优化负载配方治疗的区域的伤口闭合率显著更高(65.95±6.47%)。在体内研究中,组织病理学标本支持了之前的结果,表明通过他达拉非的血管生成活性呈现出愈合元素的级联。这些结果为临床实践中伤口治疗的新型治疗药物系统提供了深入了解。