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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Folate-molecular encapsulator-tethered biocompatible polymer grafted with magnetic nanoparticles for augmented drug delivery
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Folate-molecular encapsulator-tethered biocompatible polymer grafted with magnetic nanoparticles for augmented drug delivery

机译:叶酸分子包裹的生物相容性聚合物与磁性纳米粒子接枝以增强药物递送

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Magnetic ferrite nanoparticles (MNPs) coated with biocompatible polymers capable of drug loading and release are fascinating nanostructures for delivering anti-cancer drugs. Herein, we report the synthesis and characterization of a novel β-cyclodextrin-folate-tethered dextran polymer. Nickel–zinc ferrite nanoparticles are prepared and coated with the polymer to form a biocompatible hybrid magnetic nanocarrier. To establish the significance of folate unit of the polymer in anticancer activity, a similar derivatized polymer, i.e. β-cyclodextrin-dextran conjugate without folate tether is used for comparison. The size of the hybrid MNPs is ~20?nm, which is a size suitable for cancer drug targeting. The polymer-coated magnetic nanocarriers are soft ferromagnets as suggested by their narrow magnetic hysteresis loops. The anticancer drug camptothecin (CPT) is loaded on the magnetic nanocarriers. The drug loading efficiency is observed to be above 92%. The nanocarriers show sustained in vitro drug release for above 45?h. The in vitro cytotoxicity studies reveal that the loaded CPT retains its potency in the nanocarrier and the folate-tethered nanocarrier shows better anticancer activity than the one which does not carry a folate unit. The magnetic nanocarrier is suitable for magnetic field-guided drug transport, enhanced drug loading and release and folate receptor-mediated endocytotic uptake of drugs by cancer cells.
机译:涂有能够负载和释放药物的生物相容性聚合物的磁性铁氧体纳米颗粒(MNP)是引人注目的纳米结构,可用于输送抗癌药物。在本文中,我们报告了新型β-环糊精-叶酸酯系右旋糖酐聚合物的合成与表征。制备了镍锌铁氧体纳米颗粒,并用该聚合物涂覆以形成生物相容的杂化磁性纳米载体。为了确定该聚合物的叶酸单元在抗癌活性中的重要性,使用一种类似的衍生聚合物,即没有叶酸系链的β-环糊精-葡聚糖缀合物进行比较。杂合MNP的大小为〜20μnm,适合癌药靶向。涂覆有聚合物的磁性纳米载体是柔软的铁磁体,如其狭窄的磁滞回线所示。喜树碱喜树碱(CPT)被装载在磁性纳米载体上。观察到载药效率高于92%。纳米载体表现出持续的体外药物释放超过45?h。体外细胞毒性研究表明,负载的CPT在纳米载体中保留了其潜能,而叶酸拴系的纳米载体显示出比未携带叶酸单元更好的抗癌活性。磁性纳米载体适用于磁场引导的药物转运,增强的药物装载和释放以及叶酸受体介导的癌细胞对药物的内吞摄取。

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