4.4 Article

Interlaboratory comparison of size and surface charge measurements on nanoparticles prior to biological impact assessment

期刊

JOURNAL OF NANOPARTICLE RESEARCH
卷 13, 期 7, 页码 2675-2687

出版社

SPRINGER
DOI: 10.1007/s11051-011-0423-y

关键词

Nanoparticle; Particle surface charge; Interlaboratory comparison; Reproducibility; Polydispersity; Toxicology; Health and safety implications

资金

  1. NIEHS [RC2 ES018741, R01 ES016746, RC2 ES018766]
  2. NSF
  3. EPA [EF 0830117]
  4. EU
  5. National Cancer Institute
  6. National Institutes of Health [N01-CO-12400]
  7. German Research Foundation (DFG)
  8. Focus Project [SPP1313]
  9. [NCI R01 CA134218]
  10. [SFI 07 SRC B1155]
  11. [NMP4-SL-2008-214547]
  12. Direct For Biological Sciences
  13. Div Of Biological Infrastructure [0830117] Funding Source: National Science Foundation
  14. Div Of Biological Infrastructure
  15. Direct For Biological Sciences [830093] Funding Source: National Science Foundation

向作者/读者索取更多资源

The International Alliance for NanoEHS Harmonization (IANH) organises interlaboratory comparisons of methods used to study the potential biological impacts of nanomaterials. The aim of IANH is to identify and reduce or remove sources of variability and irreproducibility in existing protocols. Here, we present results of the first IANH round robin studies into methods to assess the size and surface charge of suspended nanoparticles. The test materials used (suspensions of gold, silica, polystyrene, and ceria nanoparticles, with [primary] particles sizes between 10 nm and 80 nm) were first analysed in repeatability conditions to assess the possible contribution of between-sample heterogeneity to the between-laboratory variability. Reproducibility of the selected methods was investigated in an interlaboratory comparison between ten different laboratories in the USA and Europe. Robust statistical analysis was used to evaluate within- and between-laboratory variability. It is shown that, if detailed shipping, measurement, and reporting protocols are followed, measurement of the hydrodynamic particle diameter of nanoparticles in predispersed monomodal suspensions using the dynamic light scattering method is reproducible. On the other hand, measurements of more polydisperse suspensions of nanoparticle aggregates or agglomerates were not reproducible between laboratories. Ultrasonication, which is commonly used to prepare dispersions before cell exposures, was observed to further increase variability. The variability of the zeta potential values, which were also measured, indicates the need to define better surface charge test protocols and to identify sources of variability.

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