Rehman Khurram, Zulfakar Mohd Hanif
Lahore Pharmacy College (A Project of Lahore Medical and Dental College), Tulspura Canal Bank, Lahore, 53400, Pakistan.
Centre for Drug Delivery Research, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, 50300, Kuala Lumpur, Malaysia.
Pharm Res. 2017 Jan;34(1):36-48. doi: 10.1007/s11095-016-2036-8. Epub 2016 Sep 12.
To characterize bigel system as a topical drug delivery vehicle and to establish the immunomodulatory role of imiquimod-fish oil combination against skin cancer and inflammation resulting from chemical carcinogenesis.
Imiquimod-loaded fish oil bigel colloidal system was prepared using a blend of carbopol hydrogel and fish oil oleogel. Bigels were first characterized for their mechanical properties and compared to conventional gel systems. Ex vivo permeation studies were performed on murine skin to analyze the ability of the bigels to transport drug across skin and to predict the release mechanism via mathematical modelling. Furthermore, to analyze pharmacological effectiveness in skin cancer and controlling imiquimod-induced inflammatory side effects, imiquimod-fish oil combination was tested in vitro on epidermoid carcinoma cells and in vivo in Swiss albino mice cancer model.
Imiquimod-loaded fish oil bigels exhibited higher drug availability inside the skin as compared to individual imiquimod hydrogel and oleogel controls through quasi-Fickian diffusion mechanism. Imiquimod-fish oil combination in bigel enhanced the antitumor effects and significantly reduced serum pro-inflammatory cytokine levels such as tumor necrosis factor-alpha and interleukin-6, and reducing tumor progression via inhibition of vascular endothelial growth factor. Imiquimod-fish oil combination also resulted in increased expression of interleukin-10, an anti-inflammatory cytokine, which could also aid anti-tumor activity against skin cancer.
Imiquimod administration through a bigel vehicle along with fish oil could be beneficial for controlling imiquimod-induced inflammatory side effects and in the treatment of skin cancer.
将双凝胶体系表征为一种局部给药载体,并确立咪喹莫特 - 鱼油组合对化学致癌引起的皮肤癌和炎症的免疫调节作用。
使用卡波姆水凝胶和鱼油油凝胶的混合物制备负载咪喹莫特的鱼油双凝胶胶体体系。首先对双凝胶的机械性能进行表征,并与传统凝胶体系进行比较。在鼠皮上进行体外渗透研究,以分析双凝胶将药物转运穿过皮肤的能力,并通过数学建模预测释放机制。此外,为了分析对皮肤癌的药理有效性以及控制咪喹莫特诱导的炎症副作用,在体外对表皮样癌细胞进行了咪喹莫特 - 鱼油组合测试,并在瑞士白化小鼠癌症模型中进行了体内测试。
与单独的咪喹莫特水凝胶和油凝胶对照相比,负载咪喹莫特的鱼油双凝胶通过准菲克扩散机制在皮肤内表现出更高的药物利用率。双凝胶中的咪喹莫特 - 鱼油组合增强了抗肿瘤作用,并显著降低了血清促炎细胞因子水平,如肿瘤坏死因子 -α 和白细胞介素 -6,并通过抑制血管内皮生长因子减少肿瘤进展。咪喹莫特 - 鱼油组合还导致抗炎细胞因子白细胞介素 -10 的表达增加,这也有助于对皮肤癌的抗肿瘤活性。
通过双凝胶载体与鱼油一起施用咪喹莫特可能有利于控制咪喹莫特诱导的炎症副作用以及治疗皮肤癌。