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粘性测量问题:团聚纳米颗粒的数浓度

Sticky Measurement Problem: Number Concentration of Agglomerated Nanoparticles.

作者信息

Minelli Caterina, Bartczak Dorota, Peters Ruud, Rissler Jenny, Undas Anna, Sikora Aneta, Sjöström Eva, Goenaga-Infante Heidi, Shard Alexander G

机构信息

National Physical Laboratory , Hampton Road , Teddington TW11 0LW , U.K.

LGC Limited , Queens Road , Teddington TW11 0LY , U.K.

出版信息

Langmuir. 2019 Apr 9;35(14):4927-4935. doi: 10.1021/acs.langmuir.8b04209. Epub 2019 Mar 26.

Abstract

Measuring the number concentration of colloidal nanoparticles (NPs) is critical for assessing reproducibility, enabling compliance with regulation, and performing risk assessments of NP-enabled products. For nanomedicines, their number concentration directly relates to their dose. However, the lack of relevant reference materials and established traceable measurement approaches make the validation of methods for NP number concentration difficult. Furthermore, commercial products often exhibit agglomeration, but guidelines for dealing with nonideal samples are scarce. We have compared the performance of five benchtop measurement methods for the measurement of colloidal number concentration in the presence of different levels of agglomeration. The methods are UV-visible spectroscopy, differential centrifugal sedimentation, dynamic light scattering, particle tracking analysis, and single-particle inductively coupled plasma mass spectrometry. We find that both ensemble and particle-by-particle methods are in close agreement for monodisperse NP samples and three methods are within 20% agreement for agglomerated samples. We discuss the sources of measurement uncertainties, including how particle agglomeration affects measurement results. This work is a first step toward validation and expansion of the toolbox of methods available for the measurement of real-world NP products.

摘要

测量胶体纳米颗粒(NP)的数量浓度对于评估可重复性、确保符合法规以及对含NP产品进行风险评估至关重要。对于纳米药物而言,其数量浓度直接关系到剂量。然而,缺乏相关参考材料以及既定的可溯源测量方法使得NP数量浓度测量方法的验证变得困难。此外,商业产品常常呈现团聚现象,但处理非理想样品的指南却很稀缺。我们比较了五种台式测量方法在不同团聚水平下测量胶体数量浓度的性能。这些方法包括紫外可见光谱法、差示离心沉降法、动态光散射法、粒子追踪分析法和单颗粒电感耦合等离子体质谱法。我们发现,对于单分散NP样品,总体方法和逐个粒子方法的结果非常一致,对于团聚样品,三种方法的结果在20%的偏差范围内。我们讨论了测量不确定度的来源,包括粒子团聚如何影响测量结果。这项工作是朝着验证和扩展可用于测量实际NP产品的方法工具箱迈出的第一步。

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