Anwer Md Khalid, Aldawsari Mohammed F, Iqbal Muzaffar, Almutairy Bjad K, Soliman Gamal A, Aboudzadeh M Ali
Department of Pharmaceutics, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-kharj 11942, Saudi Arabia.
Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Gels. 2023 Jan 22;9(2):95. doi: 10.3390/gels9020095.
The wound-healing process is complex and prone to interruption or failure, which can result in the development of chronic wounds that never heal. This can be overcome by seeking prompt medical attention, which will reduce the likelihood of complications and speed up the healing of the cutaneous wound. It has been established that functionalized engineered biomaterials are a possible strategy for starting skin wound care. The purpose of the current study is to develop a diosmin (DSM)-loaded nanoemulsion (NE)-based gel formulation and to investigate its wound healing and anti-inflammatory activity on rats. The DSM-loaded NEs (F1-F17) were developed and optimized with the help of Box-Behnken Design Expert. The DSM-Nes were developed using lauroglycol 90 (LG90) as oil, Tween-80 as surfactant and transcutol-HP (THP) as co-surfactant. The optimized Nes showed globule size (41 ± 0.07 nm), polydispersity index (PDI) (0.073 ± 0.008) and percentage of entrapment efficiency (%EE) (87 ± 0.81%). This optimized DSM-loaded NEs (F1) was further evaluated and incorporated into 1% carbopol 940 gel. F1-loaded gel was then characterized for drug content, spreadability, in vitro release, wound healing, and anti-inflammatory studies. The developed gel of DSM was found to show significantly better ( < 0.05) wound-healing and anti-inflammatory activity.
伤口愈合过程复杂且容易中断或失败,这可能导致慢性伤口的形成且永远无法愈合。通过及时寻求医疗护理可以克服这一问题,这将降低并发症的可能性并加速皮肤伤口的愈合。已经确定功能化工程生物材料是启动皮肤伤口护理的一种可能策略。本研究的目的是开发一种基于载有地奥司明(DSM)的纳米乳液(NE)的凝胶制剂,并研究其对大鼠的伤口愈合和抗炎活性。借助Box-Behnken设计专家开发并优化了载有DSM的NE(F1-F17)。使用月桂二醇90(LG90)作为油相、吐温80作为表面活性剂和二乙二醇单乙基醚(THP)作为助表面活性剂来制备DSM-NE。优化后的NE显示出粒径(41±0.07 nm)、多分散指数(PDI)(0.073±0.008)和包封率(%EE)(87±0.81%)。将这种优化后的载有DSM的NE(F1)进一步评估并掺入1%卡波姆940凝胶中。然后对载有F1的凝胶进行药物含量、铺展性、体外释放、伤口愈合和抗炎研究。发现所开发的DSM凝胶显示出显著更好(<0.05)的伤口愈合和抗炎活性。