Evidence map›Paper›PMID 41173840›Full record

ArticleNature communications2025

Multicolor cathodoluminescence imaging of single lanthanide nanoparticles.

Sohaib Abdul Rehman, Jeremy B Conway, Amy Nichols, Edward R Soucy, Amanda Dee, Kristal Stevens, Simon Merminod, Isabella MacNaughton, Abigail Curtis, Maxim B Prigozhin

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Lanthanide Nanotheranostics in Radiotherapy.International journal of molecular sciences · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sohaib Abdul Rehman *Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.
Jeremy B Conway *Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-6258-9442
Amy NicholsDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.
Edward R SoucyCenter for Brain Science, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-1187-5596
Amanda DeeDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.
Kristal StevensDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.
Simon MerminodDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0003-2706-3354
Isabella MacNaughtonDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.
Abigail CurtisDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.
Maxim B PrigozhinDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA. maxim_prigozhin@harvard.edu.ORCID http://orcid.org/0000-0002-4808-3197

Funding

HPF-X: High-pressure freezing with buffer exchangeR01GM146791 · NIGMS · HARVARD UNIVERSITY · PI Maxim Prigozhin · 2022 to 2026
$1.8M
Novel Nano- and Immuno-Probes for Multicolor Electron Microscopy of Neural Cells and TissuesR01NS134846 · NINDS · HARVARD UNIVERSITY · PI Maxim Prigozhin · 2025 to 2026
$1.2M
Dynamic nanoscale cellular imaging via time-resolved cryo-vitrificationR01GM154030 · NIGMS · HARVARD UNIVERSITY · PI Maxim Prigozhin · 2024 to 2026
$1.0M
Engineering fluid dynamics of cryo-plunging for improved vitrificationR21GM146127 · NIGMS · HARVARD UNIVERSITY · PI PRIGOZHIN, MAXIM, RYCROFT, CHRISTOPHER HARLEY · 2022 to 2023
$413k
NIGMS NIH HHS R01 GM146791NIGMS NIH HHS R01 GM154030NIGMS NIH HHS R21 GM146127NINDS NIH HHS R01 NS134846U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS134846
6 · The paper itself

Abstract

Cathodoluminescence (CL) microscopy offers a promising approach to nanoscale analysis, enabling detection of optical emission from a sample while leveraging the high resolution of electron microscopy. However, achieving multicolor single-particle CL imaging remains a significant challenge. Here, using lanthanide nanoparticles as a model system, we identify a critical limitation in CL imaging: nonlocal signal caused by stray electrons. We mitigate these nonlocal excitations and demonstrate multicolor single-particle CL imaging of nanoparticles down to 12 nm in diameter. Using this enhanced sensitivity, we demonstrate that CL brightness increases monotonically with nanoparticle diameter. We propose that multicolor imaging of spectrally distinct nanoparticles in the same field of view, coupled with the scaling of CL brightness with nanoparticle size, is crucial for confirming single-particle CL detection. Finally, we demonstrate the utility of our findings by imaging lanthanide nanoparticles in a biological sample. This work advances our understanding of nanoscale photonic responses to free electrons, establishing CL as a useful contrast mechanism for high-resolution, multicolor electron microscopy.

Identifiers

PMID41173840
PMCPMC12578839

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.