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作 者:典灵辉[1] 林晓[1] 于恩江[1] 罗京彪 华玉[1]
机构地区:[1]广东医学院药学院,东莞523808
出 处:《食品科技》2014年第11期105-109,共5页Food Science and Technology
基 金:东莞市国际合作项目(201350815200121);东莞市医疗卫生科技计划项目(201410515200139);广东医学院青年基金项目(KY20140203)
摘 要:为了增加姜黄素溶解度和稳定性,采用薄膜分散法制备姜黄素纳米粒;采用粒径测定仪、透射电镜、X-射线衍射(XRD)对其进行表征,采用UV法测定纳米粒的包封率和载药量,采用动态膜透析法考察载药纳米粒的体外释药特性。制备的纳米粒呈球形或类球形,平均粒径为(61.52±2.76)nm,平均包封率为(89.95±3.57)%,平均载药量(5.62±1.02)%;XRD结果表明,姜黄素以无定型状态或分子状态包载在纳米粒中;体外释放结果表明姜黄素的纳米粒具有明显缓释作用。该纳米粒制备工艺简单,其粒径、包封率、载药量可控,具有缓释作用。To prepare curcumin-loaded nanoparticles(Cur-NPs) and evaluate their characters in vitro. The Cur-NPs were prepared by film dispersion method. The Cur-NPs were characterized by dynamic light scattering, transmission electron microscopy(TEM), X-ray diffraction(XRD). The release curve was determined by dialysis. Entrapment efficiency and drug loading were determined by UV. The Cur-NPs observed by TEM were spherical with a mean particle size of(61.52±2.76) nm, the entrapment efficiency(EE) and drug loading of Cur-NPs were(89.95±3.57)% and(5.62±1.02)%. Release of Cur-NPs exhibited sustained release effect. X-ray diffraction determined that curcumin was in an amorphous or molecular form within the NPs. The Cur-NPs prepared had exhibited sustained release in vitro, and the particle size, encapsulation efficiency, and drug loading are controllable.
分 类 号:TS202.3[轻工技术与工程—食品科学]
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