Materials Science and Engineering , North Carolina State University , Raleigh , North Carolina 27606 , United States.
ACS Nano. 2019 Feb 26;13(2):1795-1804. doi: 10.1021/acsnano.8b07876. Epub 2019 Jan 10.
In contrast to small-molar-mass compounds, detailed structural investigations of inorganic core-organic ligand shell hybrid nanoparticles remain challenging. The assessment of batch-reaction-induced heterogeneities of surface chemical properties and their correlation with particle size has been a particularly long-standing issue. Applying a combination of high-performance liquid chromatography (HPLC) and gel permeation chromatography (GPC) to ultra-small (<10 nm diameter) poly(ethylene glycol)-coated (PEGylated) fluorescent core-shell silica nanoparticles, we elucidate here previously unknown surface heterogeneities resulting from varying dye conjugation to nanoparticle silica cores and surfaces. Heterogeneities are predominantly governed by dye charge, as corroborated by molecular dynamics simulations. We demonstrate that this insight enables the development of synthesis protocols to achieve PEGylated and targeting ligand-functionalized PEGylated silica nanoparticles with dramatically improved surface chemical homogeneity, as evidenced by single-peak HPLC chromatograms. Because surface chemical properties are key to all nanoparticle interactions, we expect these methods and fundamental insights to become relevant to a number of systems for applications, including bioimaging and nanomedicine.
与小摩尔质量的化合物相比,详细的无机核-有机配体壳混合纳米粒子的结构研究仍然具有挑战性。评估批反应诱导的表面化学性质的不均匀性及其与粒径的相关性一直是一个特别长期存在的问题。本研究应用高效液相色谱(HPLC)和凝胶渗透色谱(GPC)对超小(<10nm 直径)聚(乙二醇)包覆(PEGylated)荧光核壳二氧化硅纳米粒子进行分析,阐明了以前未知的由纳米粒子二氧化硅核和表面上的染料接枝变化引起的表面不均匀性。不均匀性主要由染料电荷控制,分子动力学模拟对此进行了证实。我们证明,这种见解可以开发合成方案,以实现具有显著改善的表面化学均一性的 PEGylated 和靶向配体功能化的 PEGylated 硅纳米粒子,这可通过 HPLC 单峰色谱图得到证明。因为表面化学性质是所有纳米粒子相互作用的关键,我们预计这些方法和基本见解将对许多应用系统(包括生物成像和纳米医学)变得相关。