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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >A method for controlling the aggregation of gold nanoparticles: Tuning of optical and spectroscopic properties
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A method for controlling the aggregation of gold nanoparticles: Tuning of optical and spectroscopic properties

机译:控制金纳米粒子聚集的方法:光学和光谱性质的调整

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Gold nanoparticles (AuNPs) have many interesting optical properties, which are derived from their surface plasmon resonance (SPR). However, the SPR of single AuNPs occurs around 520 nm, which is a limitation for biomedical imaging applications, because the maximum falls outside the tissue transparency window (~650-1000 nm). Here the aggregation of AuNPs is mediated by balancing aggregation and steric stabilization processes. This is achieved by varying the relative amounts of hydrophobic small molecules, which act as aggregating agents, and end functional hydrophilic polymers that serve as steric stabilizing agents. This approach allows the position of the SPR shifted into the tissue transparency window, while maintaining colloidal stability. Importantly, increased depolarized scattering and surface enhanced Raman scattering (SERS) cross sections in this region are achieved compared to the single nanoparticles. By varying the structure of the aggregating agent slightly, the SERS spectra exhibit significant changes, thus demonstrating the potential to encode different aggregates. The aggregates have potential applications in biomedical imaging, as an encoding strategy for combinatorial chemistry, and for use in flow cytometry applications.
机译:金纳米粒子(AuNPs)具有许多有趣的光学特性,这些特性源自其表面等离振子共振(SPR)。但是,单个AuNPs的SPR发生在520 nm左右,这是生物医学成像应用的局限性,因为最大值落在组织透明窗之外(〜650-1000 nm)。在这里,AuNP的聚集通过平衡聚集和空间稳定过程来调节。这是通过改变用作聚集剂的疏水性小分子和用作空间稳定剂的末端官能亲水性聚合物的相对量来实现的。这种方法允许SPR的位置移入组织透明窗口,同时保持胶体稳定性。重要的是,与单个纳米颗粒相比,在该区域中实现了增加的去极化散射和表面增强的拉曼散射(SERS)横截面。通过稍微改变聚集剂的结构,SERS光谱显示出显着变化,从而证明了编码不同聚集体的潜力。聚集体在生物医学成像中具有潜在的应用,可作为组合化学的编码策略,并可用于流式细胞仪。

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