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Controlled drug delivery via remotely heated core-shell magnetic microcapsules

机译:通过远程加热的核壳磁性微胶囊控制药物输送

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We report the development of magnetically-driven, 100µm in typical diameter, core-shell microcapsules for the on-demand and local delivery of encapsulated drug agents. These microcapsules are fabricated through a multi-stage microfluidic/optofluidic flow-focusing device with oil-based core and thermoresponsive polymer shell. In the prototype capsules, the shell structure is constructed by UV-curable polyethylene glycol diacrylate (PEGDA) with embedded 20%w/w poly N-isopropylacrylamide (PNIPAm) nanogels and 0.5%w/w magnetic iron oxide nanoparticles (10 nm in diameter). Experimentally, the releases of the oil fluorescent dye from the core of the capsules have been successfully demonstrated by remotely triggering the capsules with induction heating. As such, this drug delivery scheme could be useful for remotely-triggered, site-specific applications.
机译:我们报道了直径为100μm的电磁驱动核壳微胶囊的开发,该胶囊用于按需和局部递送封装的药物。这些微胶囊是通过具有油基芯和热敏性聚合物壳的多级微流/光流聚焦装置制造的。在原型胶囊中,壳结构由可紫外固化的聚乙二醇二丙烯酸酯(PEGDA)构成,内含20%w / w的聚N-异丙基丙烯酰胺(PNIPAm)纳米凝胶和0.5%w / w的磁性氧化铁纳米颗粒(直径为10 nm) )。实验上,通过感应加热远程触发胶囊,已成功证明了油性荧光染料从胶囊核心释放出来。这样,该药物输送方案对于远程触发的,针对特定地点的应用可能是有用的。

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