普鲁兰
结合
渗滤
化学
纳米颗粒
药物输送
粒径
核化学
磺胺
毒品携带者
色谱法
纳米技术
材料科学
立体化学
有机化学
生物化学
多糖
数学分析
数学
物理化学
膜
微滤
作者
Liang Liu,Peng Jin,Ming Cheng,Guoliang Zhang,Fengbao Zhang
标识
DOI:10.1016/s1004-9541(06)60086-4
摘要
In order to improve the cancer-targeting and selective activity of antineoplastic agent [5-fluorouracil (5-FU)], a novel pH-responsive drug delivery system [pullulan acetate/sulfonamide (PA/SDM) conjugate] was synthesized by a diafiltration method. Sulfonamide was grafted to the hydrophobically modified pullulan acetate to enhance the pH sensitivity for better cancer-targeting delivery. 5-FU was loaded into the self-assembled nanoparti-cles by the same method. The drug-loaded self-assembled nanoparticles were successfully obtained and characterized in terms of particle size, morphology and drug loading and release profile at various pHs. The results showed that the mean diameter of the self-assembled particles was approximately 100nm, with uniform size and good spherical morphology. The nanoparticles showed good stability at pH 7.4, which is equal to that of the normal body fluid, but shrank and aggregated below pH 6.8, which is close to the pH with tumors. The loading efficiency and concentration of released 5-FU was monitored at 269 nm on the UV/Vis spectrophotometer. The release profile was heavily pH-dependent around physiological pH, and the release rate was significantly enhanced under pH of 6.8.
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