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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Design of pH/reduction dual-responsive nanoparticles as drug delivery system for DOX: Modulating controlled release behavior with bimodal drug-loading
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Design of pH/reduction dual-responsive nanoparticles as drug delivery system for DOX: Modulating controlled release behavior with bimodal drug-loading

机译:DOX药物递送系统的pH /抑制双响应纳米粒子的设计:双峰药物负载调节控制释放行为

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Graphical abstractDisplay OmittedHighlights?Polymer nanoparticles with multifarious functional groups were designed.?The effect of the drug-loading modes on the DDSs was investigated.?Tailored controlled release behavior was achievedviathe bimodal drug-loading.AbstractpH/Reduction dual-responsive P(FPA-co-PEGMA-co-MAA) (PFPM) nanoparticles were designed for tumor-specific intracellular triggered release of anticancer drug DOX by emulsion copolymerization of 4-formylphenyl acrylate (FPA), methacrylic acid (MAA), and poly(ethylene glycol) methyl ether methacrylate (PEGMA), withN,N-bis(acryloyl)
机译:<![cdata [ 图形抽象 显示省略 突出显示 设计了具有多种官能团的聚合物纳米颗粒。 调查了药物加载模式对DDS的效果。< / ce:para> 通过斜体>斜体>斜视药物加载量定制的控制释放行为。 抽象 < CE:Abstract-SEC ID =“ABST0015”View =“全部”> pH /缩减双响应P(FPA- Co < / ce:斜体> -pegma- co <​​/ ce:斜视> -maa)(pfpm)纳米粒子被设计用于丙烯酸4-甲酰基苯乙烯酯的乳液共聚(FPA)的乳液共聚(FPA) ),甲基丙烯酸(MAA)和聚(乙二醇)甲基醚甲基丙烯酸甲酯(PEGMA),具有 n n -bis(丙烯酰基)

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