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Structure-Property Relationships of Amphiphilic Nanoparticles That Penetrate or Fuse Lipid Membranes

机译:渗透或保险丝脂膜的两亲纳米粒子的结构 - 性质关系

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摘要

The development of synthetic nanomaterials that could embed within, penetrate, or induce fusion between membranes without permanent disruption would have great significance for biomedical applications. Here we describe structure-function relationships of highly water-soluble gold nanopartides comprised of an similar to 1.5-5 nm diameter metal core coated by an amphiphilic organic ligand shell, which exhibit membrane embedding and fusion activity mediated by the surface ligands. Using an environment-sensitive dye anchored within the ligand shell as a sensor of membrane embedding, we demonstrate that particles with core sizes of similar to 2-3 nm are capable of embedding within and penetrating fluid bilayers. At the nanoscale, these particles also promote spontaneous fusion of liposomes or spontaneously embed within intact liposomal vesides. These studies provide nanoparticle design and selection principles that could be used in drug delivery applications, as membrane stains, or for the creation of novel organic/inorganic nanomaterial self-assemblies.
机译:可以在没有永久破坏的膜之间嵌入,渗透或诱导熔体之间的合成纳米材料的发展对于生物医学应用具有重要意义。在这里,我们描述了由两亲有机配体壳涂覆的类似于1.5-5nm直径的金属芯的高度水溶性金纳米粒子的结构函数关系,其表现出由表面配体介导的膜嵌入和融合活性。使用锚固在配体壳内的环境敏感染料作为膜嵌入的传感器,我们证明具有类似于2-3nm的核心尺寸的颗粒能够嵌入内部和穿透的流体双层。在纳米级,这些颗粒还促进脂质体的自发融合或自发地嵌入完整的脂质体膜中。这些研究提供了可用于药物递送应用的纳米粒子设计和选择原理,作为膜污渍,或用于产生新的有机/无机纳米材料自我组件。

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