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首页> 外文期刊>Current Nanomaterials >Thermally Activated Noble Metal Nanoparticles Incorporated in Electro-spun Fiber-based Drug Delivery Systems
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Thermally Activated Noble Metal Nanoparticles Incorporated in Electro-spun Fiber-based Drug Delivery Systems

机译:掺入电纺丝纤维的药物递送系统中的热活化贵金属纳米颗粒

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Background: Nanosystems based on PEG-PLGA copolymer have attracted increasing interest in several biomedicine fields, due to their unique properties. Commonly, PEG-PLGA copolymer was used to formulate nanoparticles (NPs) for drug delivery applications. Only recently, the engineering of polymeric nanofibrous membrane able to be use like drug nanocarrier was investigated. Objective: The goal of this work is the development of two new drug delivery systems based on PEGylated-PLGA nanofibrous scaffolds, obtained by electrospinning deposition, simultaneous loaded with: i) silibinin, a therapeutic agent, ii) Au/Ag and iii) non-toxic Fe203 magnetic nanoparticles. Another interest aspect of the present work regards how the morphological structure can influence the drug release which has been fine-tuned by two external stimuli: a light source and a magnetic field. Methods: Noble metal nanocolloids were prepared in water by the pulsed laser ablation technique. The PEG-PLGA@Au/Ag-SLB added with Fe2C>3-PVA nanofibers were fabricated by the electrospinning deposition method. Results: The use of "Surface Plasmon Resonance"-mediated localized photothermal effect, determined by the nanoparticles resonant absorption of visible radiation, allows to these systems to be able to employ for photothermal drug delivery therapies in proximity of tumor cells. All data obtained about the fiber scaffolds are compared to NPs based on the same PEG-PLGA copolymer, loaded with silibinin, Fe2O3 and Au/Ag nanoparticles alternatively. Nanofibers respects to NPs, showed interesting sustained responsive silibinin release for at least 60 h, without the burst effect. A diffusion-based theoretical model approach allowed to precisely describe the release mechanism. Conclusion: The effective and controlled silibilin drug release, upon application of either light irradiation or magnetic field for a definite time interval, has been demonstrated. Under the light stimulus, the fiber-shaped nanosystem reached a cumulative drug release value as high as 70% in the long time. On the overall, the information obtained could be useful to design suitable "on demand" nanocomposites in view of a therapeutic treatments protocol that requires a fast pharmacological action.
机译:背景技术由于其独特的特性,基于PEG-PLGA共聚物的纳米系统引起了几种生物医学领域的兴趣。通常,PEG-PLGA共聚物用于制备用于药物递送应用的纳米颗粒(NPS)。据目防,才研究了能够使用的聚合物纳米纤维膜的工程,如药物纳米载体。目的:这项工作的目的是通过静电纺丝沉积,同时装载:i)硅蛋白,治疗剂,II)Au / Ag和III)的两种新药物递送系统的发展。 - 氧化Fe203磁性纳米颗粒。本工作的另一个兴趣方面至关形态结构如何影响通过两个外部刺激的微调的药物释放:光源和磁场。方法:通过脉冲激光烧蚀技术在水中制备贵金属纳米胶体。通过静电纺丝沉积方法制造加入Fe2C> 3-PVA纳米纤维的PEG-PLGA @ AU / AG-SLB。结果:使用“表面等离子体共振”介导的局部光热效应,由纳米颗粒的谐振吸收确定可见辐射,允许这些系统能够用于肿瘤细胞附近的光热药物递送疗法。将关于纤维支架获得的所有数据基于相同的PEG-PLGA共聚物与硅蛋白,Fe2O3和Au / Ag纳米颗粒的相同的PEG-PLGA共聚物进行比较。纳米纤维对NPS表示,表现出有趣的持续响应性硅蛋白释放至少60小时,没有突发效应。基于扩散的理论模型方法允许精确描述释放机制。结论:已经证明了在施加明确时间间隔的光照射或磁场时的有效和受控的硅丙蛋白药物释放。在光刺激下,纤维状纳米系统在长时间达到70%的累积药物释放值。总体而言,鉴于需要快速药理学作用的治疗方法,所获得的信息可用于设计合适的“按需”纳米复合材料。

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