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Microextraction-Single Particle-Inductively Coupled Plasma-Mass Spectrometry for the Direct Analysis of Nanoparticles on Surfaces
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    Microextraction-Single Particle-Inductively Coupled Plasma-Mass Spectrometry for the Direct Analysis of Nanoparticles on Surfaces
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    • Jordan S. Stanberry
      Jordan S. Stanberry
      Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States
    • Hunter B. Andrews
      Hunter B. Andrews
      Radioisotope Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States
    • Cyril V. Thompson
      Cyril V. Thompson
      Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States
    • Brian W. Ticknor
      Brian W. Ticknor
      Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States
    • Benjamin T. Manard*
      Benjamin T. Manard
      Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States
      *Email: [email protected]
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    Analytical Chemistry

    Cite this: Anal. Chem. 2025, 97, 3, 1688–1694
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    https://doi.org/10.1021/acs.analchem.4c04794
    Published January 10, 2025
    Copyright © 2025 American Chemical Society

    Abstract

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    A novel employment of single particle-inductively coupled plasma-mass spectrometry (SP-ICP-MS) was developed, where a microextraction (ME) probe is used to sample nanoparticles from a surface and analyze them in a single analytical step. The effects of several parameters on the performance of ME-SP-ICP-MS were investigated, including the flow rate, choice of carrier solution, particle size, and the design of the microextraction probe head itself. The optimized ME-SP-ICP-MS technique was used to compare the extraction efficiency (EE, defined as the ratio of particles measured to particles deposited on the surface) of the commercial probe head to a newly designed SP polyether ether ketone (PEEK) probe head. The SP PEEK probe head was found to have increased EE compared to the commercial probe head (8.5 ± 3% vs 3.9 ± 3%, respectively). Increasing the carrier solution flow rate was found to decrease the total analysis time at the cost of decreasing EE. Extraction efficiencies for ME-SP-ICP-MS were typically 4–10%, which is similar to transport efficiencies (1–10%) for conventional SP-ICP-MS. Lastly, ME-SP-ICP-MS was employed for the analysis of nano- and microparticles. The sizes of gold nanoparticles, 30 ± 3 and 51 ± 1.9 nm (certified sizes), and iron-based microparticles, 1000 ± 50 nm (certified size), were accurately determined to be 32.2 ± 2.5, 50.8 ± 3.4, and 1030 ± 57 nm, respectively, by ME-SP-ICP-MS. This work demonstrates the potential of ME-SP-ICP-MS for the direct analysis of particles on common collection surfaces (GSR tabs, carbon planchettes, etc.) while retaining spatial information on particle distribution across the surface.

    Copyright © 2025 American Chemical Society

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    Supporting Information

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    The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.analchem.4c04794.

    • All 8 transients (which are overlaid in Figure 2a) for replicate extractions performed with 5% HNO3; all 8 transients (which are overlaid in Figure 2b) for replicate extractions performed with water, and example transient of 107Ag from an extraction, via ME-ICP-MS, of the 60 nm Ag coreshell particles (30 nm Au core) (PDF)

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    Analytical Chemistry

    Cite this: Anal. Chem. 2025, 97, 3, 1688–1694
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acs.analchem.4c04794
    Published January 10, 2025
    Copyright © 2025 American Chemical Society

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