کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2500909 | 1557317 | 2016 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Novel nanoemulsion based lipid nanosystems for favorable in vitro and in vivo characteristics of curcumin Novel nanoemulsion based lipid nanosystems for favorable in vitro and in vivo characteristics of curcumin](/preview/png/2500909.png)
• CNELNs were first prepared using a nanoemulsion-film dispersion-sonication method.
• CNELNs markedly improved the oral bioavailability of CUR.
• CNELNs obviously increased the gastro-intestinal absorption.
• CNELNs had stronger inhibitory effects on the viabilities of A549 cells than CUR.
• CNELNs might be promising nanosystems for oral delivery of CUR.
The goal of this study was to assess the enhanced elementary characteristics, in vitro release, anti-cancer cytotoxicity, in situ absorption and in vivo bioavailability of a novel nanoemulsion based lipid nanosystems containing curcumin (CNELNs) when administered orally. The CNELNs were first fabricated by loading water-in-oil nanoemulsions into lipid nanosystems using a nanoemulsion-film dispersion-sonication method. The gastro-intestinal absorption, in vitro release and in vivo kinetic property of CNELNs were investigated using an in situ perfusion method, a dialysis method and a concentration-time curve based method, respectively. The inhibitory effects of CNELNs on human lung cancer A549 cell growth were determined using MTT assay. The absorption constants and effective permeabilities of CNELNs in different gastro-intestinal tracts increased 2.29–4.04 times and 4.06–8.27 times that of curcumin (CUR), respectively. The relative bioavailability of CNELNs to free CUR was 733.59%. CNELNs inhibited A549 growth in a dose- and time-dependent manner. CNELNs markedly improved the oral bioavailability of CUR which was probably due to the increased gastro-intestinal absorption. CNELNs had stronger inhibitory effects on the viabilities of A549 cells than that of free CUR. CNELNs might be promising nanosystems for oral delivery of CUR to satisfy clinical requirements.
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Journal: International Journal of Pharmaceutics - Volume 504, Issues 1–2, 17 May 2016, Pages 80–88