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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >In situ preparation of magnetic Fe_3O_4 nanoparticles inside nanoporous poly(L-glutamic acid)/chitosan microcapsules for drug delivery
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In situ preparation of magnetic Fe_3O_4 nanoparticles inside nanoporous poly(L-glutamic acid)/chitosan microcapsules for drug delivery

机译:纳米多孔聚(L-谷氨酸)/壳聚糖微胶囊内原位制备磁性Fe_3O_4纳米粒子

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The magnetic polymer microcapsules, as a promising environmental stimuli-responsive delivery vehicle, have been increasingly exploited to tackle the problem of remotely navigated delivery. This study presented a novel design and fabrication of magnetic poly(L-glutamic acid)/chitosan (PGA/CS) microcapsules. Magnetic Fe_3O_4 nanoparticles were in situ synthesized inside nanoporous PGA/CS microcapsules and resultant magnetic PGA/CS microcapsules were characterized. Mitoxantrone (MTX), an antineoplastic drug, was chosen as a water-soluble model drug to research the loading and release properties of the microcapsules. The results showed the carboxylate groups of PGA within polyelectrolyte walls could be used as binding sites for the absorption of iron ions and reaction sites for the synthesis of magnetic nanoparticles. Magnetic PGA/CS microcapsules were dissected using a dual-beam scanning electron microscope/focused ion beam (SEM/FIB) for morphological and microstructural examination. It was found that Fe_3O_4 nanoparticles with size of about 10nm were homogeneously dispersed in the polymer matrix and adhered to the pore walls of the microcapsules. Increasing the concentration of iron ions led to an increasing loading content of Fe3 04 nanoparticles and an increase in the resultant magnetization. The magnetic PGA/CS microcapsules could be easily manipulated by an external magnetic field. The MTX loading capacity depended on loading time and MTX concentration. The high loading could be ascribed to spontaneous deposition of MTX induced by electrostatic interaction. The microcapsules exhibited sustained release behavior. The MTX release from microcapsules could be best described using Korsmeyer-Peppas and Baker-Lonsdale models, indicating the diffusion mechanism of drug release from both PGA/CS microcapsules and magnetic PGA/CS microcapsules. Therefore, the novel magnetic PGA/CS microcapsules are expected to find application in drug delivery systems because of the properties of magnetic sensitivity, high drug loading and sustained release.
机译:磁性聚合物微胶囊作为一种有前途的环境刺激响应性递送工具,已被越来越多地用于解决远程导航递送的问题。这项研究提出了磁性聚(L-谷氨酸)/壳聚糖(PGA / CS)微胶囊的新型设计和制造。在纳米多孔PGA / CS微胶囊中原位合成了磁性Fe_3O_4纳米粒子,并表征了所得的磁性PGA / CS微胶囊。选择抗肿瘤药米托蒽醌(MTX)作为水溶性模型药物,以研究微胶囊的负载和释放特性。结果表明,聚电解质壁中PGA的羧酸根可作为吸附铁离子的结合位点和磁性纳米粒子的合成反应位点。使用双电子束扫描电子显微镜/聚焦离子束(SEM / FIB)解剖磁性PGA / CS微胶囊,以进行形态学和微结构检查。发现具有约10nm的尺寸的Fe_3O_4纳米颗粒均匀地分散在聚合物基质中并粘附到微胶囊的孔壁上。铁离子浓度的增加导致Fe 3 04纳米颗粒的负载量增加,并且所得磁化强度增加。磁性PGA / CS微胶囊可通过外部磁场轻松操纵。 MTX的装载量取决于装载时间和MTX浓度。高负荷可以归因于由静电相互作用诱导的MTX的自发沉积。微胶囊表现出持续释放行为。使用Korsmeyer-Peppas和Baker-Lonsdale模型可以最好地描述MTX从微囊中释放出来,表明药物从PGA / CS微囊和磁性PGA / CS微囊中的扩散机制。因此,由于磁性敏感性,高药物载量和持续释放的特性,新型磁性PGA / CS微胶囊有望在药物递送系统中找到应用。

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