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作 者:邢晓婧[1] 宋秋荷[1] 钟白玉[1] 郝飞[1]
机构地区:[1]第三军医大学西南医院皮肤科,重庆400038
出 处:《第三军医大学学报》2011年第7期719-722,共4页Journal of Third Military Medical University
基 金:重庆市科技攻关计划项目(SWH2008003)~~
摘 要:目的制备mEGF乙醇脂质体,并研究mEGF乙醇脂质体囊泡的包封率和物理性质。方法采用高效液相色谱法(HPLC)测定mEGF乙醇脂质体的包封率、精密度、回收率、稳定性,运用扫描电镜、原子力显微镜、透射电镜和激光粒度分析仪观察和分析mEGF乙醇脂质体囊泡的外观、粒径和均一度。结果 mEGF乙醇脂质体的包封率大约为38%,精密度小于5%,30 d内包封率波动在36%~38%之间。运用原子力显微镜和透射电镜观察到粒径分布于40~60 nm的乙醇脂质体囊泡。并且在激光动态光散射仪下测定显示囊泡的粒度分布较为均一,mEGF乙醇脂质体的折光度为4.6,囊泡粒径大约分布在100~500 nm之间。结论成功制备了mEGF乙醇脂质体,建立了测定包封率的色谱方法,该给药系统稳定性较好,乙醇脂质体囊泡粒径分布均匀。Objective To prepare an ethosomal delivery system containing mouse epidermal growth factor(mEGF) and investigate its entrapment efficiency and physical properties.Methods The entrapment efficiency of mEGF ethosome(10 μg/g) was determined by high pressure liquid chromatography(HPLC).The mEGF ethosome vesicles were visualized by scanning electron microscopy(SEM),atomic force microscopy(AFM) and transmission electron microscopy(TEM).And the size distribution of ethosome vesicles was investigated using dynamic light scattering(DLS).Results The mEGF ethosome had an entrapment efficiency of 38% and the RSD was less than 5%.The entrapment efficiency of mEGF ethosomal carriers ranged from 36% to 38% during 30 d after having been prepared.mEGF ethosomal carriers had rather small vesicles in a size ranging from 40 nm to 60 nm visualized by AFM and TEM.And the size of the mEGF ethosomal delivery system had uniform distribution ranging from 100 nm to 500 nm.Also,the refractive index of the mEGF ethosomal delivery system was 4.6.ConclusionA mEGF ethosomal delivery system is successfully prepared.A HPLC method is developed to determine mEGF content in ethosomal delivery system.The delivery system shows a well stability and a narrow particle size distribution.
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