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Surface Molecularly Imprinted Polymer of Chitosan Grafted Poly(methyl methacrylate) for 5-Fluorouracil and Controlled Release

机译:壳聚糖接枝聚甲基丙烯酸甲酯用于5-氟尿嘧啶和控释的表面分子印迹聚合物

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摘要

The molecular surface imprinted graft copolymer of chitosan with methyl methacrylate (MIP-CS-g-PMMA) were prepared by free radical polymerization with 5-fluorouracil (5-FU) as the template molecule using initiator of ammonium persulfate as adsorption system. MIPs were characterized by FTIR, X-ray diffraction, thermo-gravimetric analysis, 1H NMR and SEM. The mechanism of graft copolymerization and factors affected graft reaction were studied in details, and the optimum reaction conditions (to the highest %G and %E as the standard) were obtained at [MMA] 1.2 mol/L, [Chitosan] 16.67 mol/L, [initiator] 0.0062 mol/L, temperature 60 °C and reaction time 7 h. MIPs exhibited high recognition selectivity and excellent combining affinity to template molecular. The in vitro release of the 5-FU was highly pH-dependent and time delayed. The release behavior showed that the drugs did not release in simulated gastric fluid (pH = 1.0), and the drug release was small in the simulated small intestinal fluid (pH = 6.8), and drug abrupt release will be produced in the simulated colon fluid (pH = 7.4), indicating excellent colon-specific drug delivery behavior.
机译:以过硫酸铵的引发剂为吸附体系,以5-氟尿嘧啶(5-FU)为模板分子,通过自由基聚合制备了壳聚糖与甲基丙烯酸甲酯的分子表面印迹接枝共聚物(MIP-CS-g-PMMA)。通过FTIR,X射线衍射,热重分析, 1 1 H NMR和SEM对MIP进行了表征。详细研究了接枝共聚反应的机理和影响接枝反应的因素,并以[MMA] 1.2 mol / L,[壳聚糖] 16.67 mol / L获得了最佳反应条件(以最高%G和%E为标准)。 L,[引发剂] 0.0062 mol / L,温度60 C,反应时间7 h。 MIP表现出高识别选择性和对模板分子的优异结合亲和力。 5-FU的体外释放高度依赖pH值,并且延迟时间。释放行为表明药物在模拟胃液(pH = 1.0)中没有释放,在模拟小肠液(pH = 6.8)中药物释放很小,在模拟结肠液中会产生药物突然释放。 (pH = 7.4)表示良好的结肠特异性药物递送行为。

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