首页> 外文期刊>Bulletin of the Korean Chemical Society >Real-time Monitoring of Colloidal Nanoparticles using Light Sheet Dark-field Microscopy Combined with Microfluidic Concentration Gradient Generator (μFCGG-LSDFM)
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Real-time Monitoring of Colloidal Nanoparticles using Light Sheet Dark-field Microscopy Combined with Microfluidic Concentration Gradient Generator (μFCGG-LSDFM)

机译:使用光片暗场显微镜结合微流控浓度梯度发生器(μFCGG-LSDFM)实时监测胶体纳米颗粒

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摘要

For real-time monitoring of colloidal nanoparticles (NPs) in aqueous media, a light sheet type dark-field microscopy system combined with a microfluidic concentration gradient generator (μFCGG-LSDFM) was developed. Various concentrations of colloidal Au NPs were simultaneously generated with the iFCGG and characterized with the LSDFM setup. The number concentrations and hydrodynamic size distributions were measured via particle counting and tracking analysis (PCA and PTA, respectively) approaches. For the 30 nm Au NPs used in this study, the lower detection limit of the LSDFM setup was 3.6 ng/mL, which is about 400 times better than that of optical density measurements under the same μFCGG system. Additionally, the hydrodynamic diameter distribution of Au NPs was estimated as 39.7 ± 12.2 nm with the PTA approach, which agrees well with DLS measurement as well as the manufacturer's specification. We propose this μFCGG-LSDFM setup with features of automatic generation of NP concentration gradient and real-time monitoring of their physico-chemical characteristics (e.g., number concentration, and hydrodynamic size distribution) as an important component of future high-throughput screening or high-content analysis platforms of nanotoxicity.
机译:为了实时监测水性介质中的胶体纳米颗粒(NPs),开发了一种结合了微流控浓度梯度发生器(μFCGG-LSDFM)的光片型暗场显微镜系统。 iFCGG同时生成各种浓度的胶体金纳米颗粒,并通过LSDFM装置进行表征。通过粒子计数和跟踪分析(分别为PCA和PTA)方法测量了数浓度和流体动力学尺寸分布。对于本研究中使用的30 nm Au NP,LSDFM装置的检测下限为3.6 ng / mL,比相同μFCGG系统下的光密度测量结果高约400倍。另外,通过PTA方法估计Au NPs的流体动力学直径分布为39.7±12.2 nm,这与DLS测量以及制造商的规范非常吻合。我们建议这种μFCGG-LSDFM设置具有自动生成NP浓度梯度和实时监测其理化特性(例如数量浓度和流体动力学尺寸分布)的功能,作为未来高通量筛选或高通量筛选的重要组成部分含量的纳米毒性分析平台。

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