Yang Xindu, Zhang Qiqing, Wang Yinsong, Chen Han, Zhang Huizhu, Gao Fuping, Liu Lingrong
Institute of Biomedical Engineering, Chinese Academy of Medical Sciences, Peking Union Medical College, The Key Laboratory of Biomedical Material of Tianjin, Tianjin 300192, PR China.
Colloids Surf B Biointerfaces. 2008 Feb 15;61(2):125-31. doi: 10.1016/j.colsurfb.2007.07.012. Epub 2007 Aug 3.
Methoxy poly(ethylene glycol)-grafted-chitosan (mPEG-g-CS) conjugates were synthesized by formaldehyde linking method and characterized by Fourier transform infrared (FT-IR) and proton nuclear magnetic resonance ((1)H-NMR). The degree of substitution (DS) of methoxy poly (ethylene glycol) (mPEG) in the mPEG-g-CS molecules determined by (1)H-NMR ranged from 19% to 42%. The critical aggregation concentration (CAC) was determined by fluorescence spectroscopy using pyrene as fluorescence probe and its value was 0.07 mg/mL in water. mPEG-g-CS formed monodisperse self-aggregated nanoparticles with a roughly spherical shape and a mean diameter of 261.9 nm were prepared by the dialysis method. mPEG-g-CS self-aggregated nanoparticles were used as carriers of poorly water-soluble anticancer drug methotrexate (MTX). MTX was physically entrapped inside mPEG-g-CS self-aggregated nanoparticles by dialysis method and the characteristics of MTX-loaded mPEG-g-CS self-aggregated nanoparticles were analyzed using dynamic laser light scattering (DLLS), transmission electron microscopy (TEM). Moreover, in vitro release behavior of MTX was also investigated and the results showed that MTX was continuously released more than 50% in 48 h.
采用甲醛连接法合成了甲氧基聚(乙二醇)接枝壳聚糖(mPEG-g-CS)共轭物,并通过傅里叶变换红外光谱(FT-IR)和质子核磁共振((1)H-NMR)对其进行了表征。通过(1)H-NMR测定的mPEG-g-CS分子中甲氧基聚(乙二醇)(mPEG)的取代度(DS)范围为19%至42%。以芘为荧光探针,通过荧光光谱法测定了临界聚集浓度(CAC),其在水中的值为0.07 mg/mL。通过透析法制备了具有大致球形且平均直径为261.9 nm的单分散自聚集纳米颗粒mPEG-g-CS。mPEG-g-CS自聚集纳米颗粒被用作水溶性差的抗癌药物甲氨蝶呤(MTX)的载体。通过透析法将MTX物理包封在mPEG-g-CS自聚集纳米颗粒内部,并使用动态激光光散射(DLLS)、透射电子显微镜(TEM)分析了负载MTX的mPEG-g-CS自聚集纳米颗粒的特性。此外,还研究了MTX的体外释放行为,结果表明MTX在48小时内持续释放超过50%。