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Preparation and Drug Release Properties of FesCVChitosan Magnetic Microspheres

机译:FESCVCHITOSAN磁性微球的制备和药物释放性能

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Fe3O4/chitosan(CS)magnetic microspheres were prepared by emulsion crosslinking method,in which 5-fluorouracil(5-Fu)was loaded as model drug.The preparation conditions were optimized by orthogonal experiment with the the package rate as an index.The structure and morphology of the magnetic microspheres were characterized by scanning electron microscopy(SEM).The drug release properties of the microspheres in vitro were investigated.The optimal preparation conditions of drug loaded magnetic microspheres were as follows:0.3 g 5-Fu,5 mL glutaraldehyde,3 h crosslinking time and 0.2 g/ml acetic acid concentration.Under these conditions,the drug loading efficiency was up to 6.35% as well,as the package rate was up to 35.2%.The Fe3O4/chitosan magnetic microspheres also displayed an excellent drug release behavior under the experimental conditions of simulated intestinal fluid.The releasing content reached a peak in 10 h.
机译:通过乳液交联法制备Fe3O4 /壳聚糖(CS)磁性微球,其中5-氟尿嘧啶(5-FU)作为模型药物装载。通过正交实验,用封装率作为指标进行优化的制备条件。结构 通过扫描电子显微镜(SEM)表征磁性微球的形态。研究了体外微球的药物释放性质。药物负载磁性微球的最佳制剂条件如下:0.3g 5-FU,5ml戊二醛 ,3 h交联时间和0.2g / ml乙酸浓度。这些条件下,药物负载效率也高达6.35%,因为包装速率高达35.2%。Fe3O4 /壳聚糖磁性微球也显示出优异的 在模拟肠液的实验条件下药物释放行为。释放含量在10小时内达到峰。

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