Farghaly Aly Usama, Abou-Taleb Heba A, Abdellatif Ahmed Ah, Sameh Tolba Nahla
Department of Pharmaceutics, Faculty of Pharmacy, Minia University, El-Minia, Egypt,
Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Nahda University (NUB), Beni-Suef, Egypt.
Drug Des Devel Ther. 2019 May 10;13:1567-1580. doi: 10.2147/DDDT.S198413. eCollection 2019.
The aim of this study was to formulate a hydrogel loaded with polymeric nanoparticles (PoNPs) of simvastatin (SIM) for topical wound healing application.
The SIM PoNPs were prepared by using the nanoprecipitation method to improve the drug solubility and skin permeation. Furthermore, drug content, solubility, particle size, surface charge, and transmission electron microscopy of the prepared PoNPs were evaluated. Then, the PoNPs were loaded on hydrogel, and physical characteristics, in vitro release, and ex vivo permeation of the hydrogel were evaluated. Finally, the prepared gel was applied on rat wounds, and a histopathological study was performed.
The results showed that the drug content in the PoNPs was 86.4%. The PoNPs were spherical in shape with a smooth surface and a uniform size distribution. The particle size was 268.4±2.6, polydispersity index was ≤0.302, and zeta potential was -33±1.67 mV. The hydrogel loaded with SIM PoNPs was homogenous, and the pH was accepted and compatible with the skin. Moreover, the viscosity and spreadability assured its ease of application. The drug content was 97.25±0.02%. Furthermore, about 81% of SIM was released within 24 hours, while in the ex vivo permeation study 69.19% of SIM passed through the skin after 24 hours. Finally, the histopathological studies confirmed the efficacy of the SIM PoNPs-loaded hydrogel in wound healing due to the formation of the normal epithelial layer on day 11 after wound creation.
The hydrogel loaded with SIM PoNPs showed a good efficacy in accelerating the healing of the rat wound with complete epithelialization and minimal inflammatory cell infiltration.
本研究旨在制备一种负载辛伐他汀(SIM)聚合物纳米颗粒(PoNPs)的水凝胶,用于局部伤口愈合。
采用纳米沉淀法制备SIM PoNPs,以提高药物溶解度和皮肤渗透性。此外,对制备的PoNPs的药物含量、溶解度、粒径、表面电荷和透射电子显微镜进行了评估。然后,将PoNPs负载到水凝胶上,评估水凝胶的物理特性、体外释放和离体渗透。最后,将制备的凝胶应用于大鼠伤口,并进行组织病理学研究。
结果表明,PoNPs中的药物含量为86.4%。PoNPs呈球形,表面光滑,粒径分布均匀。粒径为268.4±2.6,多分散指数≤0.302,zeta电位为-33±1.67 mV。负载SIM PoNPs的水凝胶均匀,pH值符合要求且与皮肤相容。此外,粘度和铺展性确保了其易于应用。药物含量为97.25±0.02%。此外,约81%的SIM在24小时内释放,而在离体渗透研究中,24小时后69.19%的SIM透过皮肤。最后,组织病理学研究证实了负载SIM PoNPs的水凝胶在伤口愈合中的疗效,因为在伤口形成后第11天形成了正常上皮层。
负载SIM PoNPs的水凝胶在加速大鼠伤口愈合方面显示出良好的疗效,实现了完全上皮化,炎症细胞浸润最少。