一步法合成水溶性金纳米粒子及其尺寸和表面功能控制

One-phase synthesis of water-soluble gold nanoparticles with control over size and surface functionalities.

机构信息

Division of Optical Sciences, Code 5611, U.S. Naval Research Laboratory, Washington, DC 20375, USA.

出版信息

Langmuir. 2010 May 18;26(10):7604-13. doi: 10.1021/la904438s.

Abstract

We report a simple and efficient synthetic method to prepare gold nanoparticles (AuNPs) in aqueous phase using HAuCl(4) and poly(ethylene glycol) (PEG) ligands appended with bidentate anchoring groups. Our approach provides narrow size distribution nanocrystals over the size range between 1.5 and 18 nm; this range is much wider than those achieved using other small molecules and polymer ligands. The NP size was simply controlled by varying the molar ratio of Au-to-PEG ligand precursors. Further passivation of the as-prepared AuNPs permitted in situ functionalization of the NP surface with the desired functional groups. The prepared AuNPs exhibit remarkable stability in the presence of high salt concentrations, over a wide range of pHs (2-13), and a strong resistance to competition from dithiothreitol (DTT). These results are a clear manifestation of the advantages offered by our synthetic approach to prepare biocompatible AuNPs, where modular, multifunctional ligands presenting strong anchoring groups and hydrophilic PEG chains are used.

摘要

我们报告了一种简单有效的在水相中使用 HAuCl(4) 和聚乙二醇(PEG)配体合成金纳米粒子(AuNPs)的方法,该配体带有双齿锚固基团。我们的方法提供了尺寸分布在 1.5 至 18nm 之间的纳米晶,其范围比使用其他小分子和聚合物配体的范围宽得多。通过改变 Au 与 PEG 配体前体的摩尔比,可以简单地控制 NP 的尺寸。进一步对制备的 AuNPs 进行钝化处理,允许在 NP 表面原位功能化所需的功能基团。所制备的 AuNPs 在高盐浓度、宽 pH 值范围(2-13)和对二硫苏糖醇(DTT)的强烈竞争存在下表现出显著的稳定性。这些结果清楚地表明了我们的合成方法在制备生物相容性 AuNPs 方面的优势,该方法使用了模块化、多功能配体,具有强锚固基团和亲水 PEG 链。

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