کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2504030 | 1557446 | 2010 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Physicochemical and pharmacological characterization of α-tocopherol-loaded nano-emulsion system Physicochemical and pharmacological characterization of α-tocopherol-loaded nano-emulsion system](/preview/png/2504030.png)
The main purpose of the present study is to develop a novel nano-emulsion (NE) formulation of α-tocopherol (α-TC) with enhanced oral bioavailability and pharmacological effects. Three NE formulations of α-TC at different loading amounts (10%, 30% and 50%) were prepared by a mechanochemical method. Physicochemical properties of NE formulations were characterized with a focus on the morphology by transmission electron microscopy (TEM), droplet size distribution and zeta-potential by dynamic light scattering (DLS), and long-term stability. According to the TEM images and DLS data, mean diameters of NE droplets ranged from 80 to 400 nm, in proportion to the amount of loaded α-TC. Although all NE formulations of α-TC were found to be negatively charged with the zeta-potential of ca −40 mV, NE formulations at α-TC content of 30% or higher exhibited severe aggregation of droplets in NE formulations during long-term storage. After oral administration of 10% α-TC-loaded NE formulation (30 mg α-TC/kg) in rats, higher α-TC exposure was observed with a 2.6-fold increase of bioavailability as compared to the control mixture of oil and α-TC. In streptozotocin-induced diabetic rats, oral administration of the α-TC-loaded NE formulation (30 mg α-TC/kg) exhibited a significant reduction of lipoperoxidant in several organs, especially the liver; however, the control mixture was less effective. With these findings, the NE approach might be efficacious to improve the oral bioavailability and anti-oxidative activities of α-TC.
Journal: International Journal of Pharmaceutics - Volume 396, Issues 1–2, 30 August 2010, Pages 188–193