Jeengar Manish Kumar, Shrivastava Shweta, Mouli Veeravalli S Chandra, Naidu V G M, Sistla Ramakrishna
Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education & Research, Balanagar, Hyderabad 500037, India.
KIMS Hospitals, Begumpet, Secunderabad 500003, India.
Nutrition. 2016 Sep;32(9):955-64. doi: 10.1016/j.nut.2016.02.009. Epub 2016 Mar 8.
The aim of the present study was to investigate the skin penetration potential of emu oil and the possibility of enhancing the antiarthritic potential of lipophilic bioactive curcumin, which has poor permeability through biological membranes.
Solubility and ex vivo skin permeation studies were performed with water, corn oil, and emu oil as a vehicle using curcumin as a model drug. Carrageenan induced inflammation and Freund's complete adjuvant-induced arthritic rat models were used to evaluate enhanced antiinflammatory and antiarthritic effect of curcumin in combination of emu oil via topical route.
The skin permeation study resulted in the combination of emu oil with curcumin enhancing the flux 1.84 and 4.25 times through the rat skin compared to corn oil and water, respectively. Results of carrageenan induced rat paw edema model demonstrated that percentage of paw inhibition shown by curcumin-emu oil combination was 1.42-fold more compared to the total effect shown by both groups treated with curcumin aqueous suspension and emu oil per se. In Freund's complete adjuvant-induced arthritic model, the combined treatment was effective in bringing significant changes in the functional, biochemical, histopathologic, and radiologic parameters. Topical application of curcumin-emu oil combination resulted in significant reduced levels of proinflammatory mediators TNF-α, IL-1 β, and IL-6 (P < 0.05, 0.001, and 0.01, respectively) compared to arthritic animals.
Topical delivery of curcumin with emu oil holds promise as a noninvasive and efficacious intervention for the treatment of inflammatory arthritis and it assists in further development of a topical formulation of curcumin using emu oil as a vehicle.
本研究旨在探讨鸸鹋油的皮肤渗透潜力,以及增强亲脂性生物活性姜黄素抗关节炎潜力的可能性,姜黄素通过生物膜的渗透性较差。
以水、玉米油和鸸鹋油为载体,以姜黄素为模型药物进行溶解度和体外皮肤渗透研究。采用角叉菜胶诱导的炎症和弗氏完全佐剂诱导的关节炎大鼠模型,通过局部给药途径评估姜黄素与鸸鹋油联合使用时增强的抗炎和抗关节炎作用。
皮肤渗透研究结果表明,与玉米油和水相比,鸸鹋油与姜黄素的组合使姜黄素透过大鼠皮肤的通量分别提高了1.84倍和4.25倍。角叉菜胶诱导的大鼠足爪水肿模型结果显示,姜黄素-鸸鹋油组合的足爪抑制百分比比姜黄素水悬浮液和鸸鹋油单独处理的两组的总效果高1.42倍。在弗氏完全佐剂诱导的关节炎模型中,联合治疗有效地使功能、生化、组织病理学和放射学参数发生了显著变化。与关节炎动物相比,局部应用姜黄素-鸸鹋油组合导致促炎介质肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6的水平显著降低(分别为P < 0.05、0.001和0.01)。
局部递送姜黄素与鸸鹋油有望成为治疗炎性关节炎的一种非侵入性且有效的干预措施,并有助于进一步开发以鸸鹋油为载体的姜黄素局部制剂。