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首页> 外文期刊>Scientific reports. >Nanostructured Polymer Thin Films Fabricated with Brush-based Layer-by-Layer Self-assembly for Site-selective Construction and Drug release
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Nanostructured Polymer Thin Films Fabricated with Brush-based Layer-by-Layer Self-assembly for Site-selective Construction and Drug release

机译:纳米结构聚合物薄膜的制备与基于刷的逐层自组装的站点选择性建设和药物释放。

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Layer-by-Layer (LbL) self-assembly has been investigated for several decades. However, the conventional LbL method has performance problems on the chair-side caused by its cumbersome and time-consuming process. Thus, we investigate a new LbL self-assembly technique for the fast and high efficient preparation process based on the brush. The multilayer films fabricated by simple sequential brushing of polyelectrolyte solutions are compared to the classical dipping method. We characterize the multilayer films by characteristics such as their morphology and thickness, and compare them against those of the classic method by profilometry, atomic force microscopy. We prepare multilayer films with biocompatible polyelectrolytes, chitosan, and alginate incorporated with a hydrophobic drug carrier. For the drug carrier, a poly(ethylene glycol)-block-poly(ε-caprolactone) (PEG-b-PCL) block copolymer is introduced to construct micelles containing dexamethasone, which is a well-known osteogenesis-inducing drug. The hydrogen bonding behavior between adjacent layers and micelles is investigated by Fourier transform infrared spectroscopy. Additionally, we analyze the release profiles, degradation profiles and toxicity of the multilayer films for biomedical applications. From these results, we can identify the brushing LbL method as a reliable and more efficient multilayer film-construction process compared to conventional dipping LbL, especially for practical applications in dental and clinical situations.
机译:逐层(LbL)自组装已经研究了数十年。然而,常规的LbL方法由于其麻烦且费时的过程而在椅子侧具有性能问题。因此,我们研究了一种新的基于LbL的LbL自组装技术,用于基于刷子的快速高效制备过程。将通过简单顺序刷洗聚电解质溶液制成的多层膜与传统的浸渍方法进行了比较。我们通过诸如形态和厚度等特性来表征多层膜,并通过轮廓分析,原子力显微镜将其与经典方法进行比较。我们准备了具有生物相容性聚电解质,壳聚糖和藻酸盐并结合了疏水性药物载体的多层薄膜。对于药物载体,引入聚(乙二醇)-嵌段-聚(ε-己内酯)(PEG-b-PCL)嵌段共聚物以构建含有地塞米松的胶束,地塞米松是众所周知的成骨诱导药物。通过傅立叶变换红外光谱研究相邻层和胶束之间的氢键键合行为。此外,我们分析了生物医学应用多层膜的释放曲线,降解曲线和毒性。从这些结果可以看出,与传统的浸渍LbL相比,刷涂LbL方法是一种可靠且更有效的多层膜构建工艺,尤其适用于牙科和临床情况。

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