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Cyclodextrin–PEG conjugate-wrapped magnetic ferrite nanoparticles for enhanced drug loading and release

机译:环糊精-PEG共轭物包裹的磁性铁氧体纳米粒子可增强药物的加载和释放

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Magnetic nanoparticles are envisaged to overcome the impediments in the methods of targeted drug delivery and hence cure cancer effectively. We report herein, manganese ferrite nanoparticles, coated with β-cyclodextrin-modified polyethylene glycol as a carrier for the drug, camptothecin. The particles are of the size of ~?100?nm and they show superparamagnetic behaviour. The saturation magnetization does not get diminished on polymer coverage of the nanoparticles. The β-cyclodextrin–polyethylene glycol conjugates are characterized using NMR and mass spectrometric techniques. By coating the magnetic nanoparticles with the cyclodextrin–tethered polymer, the drug-loading capacity is enhanced and the observed release of the drug is slow and sustained. The cell viability of HEK293 and HCT15 cells is evaluated and the cytotoxicity is enhanced when the drug is loaded in the polymer-coated magnetic nanoparticles. The noncovalent-binding based and enhanced drug loading on the nanoparticles and the sustained release make the nanocarrier a promising agent for carrying the payload to the target.
机译:设想磁性纳米颗粒克服靶向药物递送方法中的障碍,并因此有效治愈癌症。我们在这里报告,用β-环糊精修饰的聚乙二醇包衣作为药物喜树碱的载体的锰铁氧体纳米颗粒。粒子的大小约为100纳米,显示超顺磁性。纳米颗粒的聚合物覆盖率不会降低饱和磁化强度。 β-环糊精-聚乙二醇共轭物使用NMR和质谱技术进行表征。通过用环糊精束缚的聚合物包被磁性纳米颗粒,药物的负载能力得到增强,观察到的药物释放缓慢而持续。当药物装入聚合物包被的磁性纳米颗粒中时,评估了HEK293和HCT15细胞的细胞生存力,并增强了细胞毒性。基于非共价结合的纳米颗粒上增加的药物负载以及持续释放使纳米载体成为用于将有效载荷携带到靶标的有前途的药物。

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