Thompson S, Pappas Dimitri
Texas Tech University Department of Chemistry and Biochemistry, Lubbock, TX, USA.
RSC Adv. 2020;10(15):8735-8743. doi: 10.1039/c9ra10421f. Epub 2020 Feb 28.
Dye-doped nanoparticles have been investigated as bright, luminescent labels for super -resolution microscopy via localization methods. One key factor in super-resolution is the size of the luminescent label, which in some cases results in a frame shift between the label target and the label itself. Ag@SiO core-shell nanoparticles, doped with organic fluorophores, have shown promise as super-resolution labels. One key aspect of these nanoparticles is that they blink under certain conditions, allowing super-resolution localization with a single excitation source in aqueous solution. In this work, we investigated the effects of both the Ag core and the silica (SiO) shell on the self-blinking properties of these nanoparticles. Both core size and shell thickness were manipulated by altering the reaction time to determine core and shell effects on photoblinking. Size and shell thickness were investigated individually under both dry and hydrated conditions and were then doped with a 1 mM solution of Rhodamine 110 for analysis. We observed that the cores themselves are weakly luminescent and are responsible for the blinking observed in the fully-synthesized metal-enhanced fluorescence nanoparticles. There was no statistically significant difference in photoblinking behavior-both intensity and duty cycle-with decreasing core size. This observation was used to synthesize smaller nanoparticles ranging from approximately 93 nm to 110 nm as measured using dynamic light scattering. The blinking particles were localized via super-resolution microscopy and show single particle self-blinking behavior. As the core size did not impact blinking performance or intensity, the nanoparticles can instead be tuned for optimal size without sacrificing luminescence properties.
染料掺杂的纳米颗粒已被研究作为通过定位方法用于超分辨率显微镜的明亮发光标记。超分辨率的一个关键因素是发光标记的大小,在某些情况下,这会导致标记目标与标记本身之间出现帧移。掺杂有机荧光团的Ag@SiO核壳纳米颗粒已显示出作为超分辨率标记的潜力。这些纳米颗粒的一个关键方面是它们在某些条件下会闪烁,从而允许在水溶液中使用单一激发源进行超分辨率定位。在这项工作中,我们研究了Ag核和二氧化硅(SiO)壳对这些纳米颗粒自闪烁特性的影响。通过改变反应时间来控制核尺寸和壳厚度,以确定核和壳对光闪烁的影响。在干燥和水合条件下分别研究了尺寸和壳厚度,然后用1 mM的罗丹明110溶液进行掺杂以进行分析。我们观察到核本身发出微弱的光,并且是在完全合成的金属增强荧光纳米颗粒中观察到的闪烁的原因。随着核尺寸减小,光闪烁行为(强度和占空比)没有统计学上的显著差异。利用这一观察结果合成了通过动态光散射测量尺寸约为93 nm至110 nm的较小纳米颗粒。通过超分辨率显微镜对闪烁颗粒进行定位,并显示出单颗粒自闪烁行为。由于核尺寸不影响闪烁性能或强度,因此可以在不牺牲发光特性的情况下对纳米颗粒进行尺寸优化。