Evidence map›Paper›PMID 36660770›Full record

ArticleACS nano2023

Multispectral Localized Surface Plasmon Resonance (msLSPR) Reveals and Overcomes Spectral and Sensing Heterogeneities of Single Gold Nanoparticles.

Stephen Palani, John P Kenison, Sinan Sabuncu, Tao Huang, Fehmi Civitci, Sadik Esener, Xiaolin Nan

Abstract read
In one paragraph

Article in ACS nano, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Strategies for Multiplexing Plasmonic Biosensing.Sensors (Basel, Switzerland) · 2026
    Review
  3. Article
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  6. Article
  7. Review
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  16. Spaced Hybrid TiOACS omega · 2024
    Article
  17. Article
  18. Article
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

7 authors.

Stephen PalaniKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, 2720 S. Moody Ave., Portland, Oregon 97201, United States.
John P KenisonKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, 2720 S. Moody Ave., Portland, Oregon 97201, United States.ORCID 0000-0003-4138-6600
Sinan SabuncuKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, 2720 S. Moody Ave., Portland, Oregon 97201, United States.ORCID 0000-0001-8346-8175
Tao HuangDepartment of Biomedical Engineering, Oregon Health & Science University, 2730 S Moody Ave., Portland, Oregon 97201, United States.
Fehmi CivitciKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, 2720 S. Moody Ave., Portland, Oregon 97201, United States.
Sadik EsenerKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, 2720 S. Moody Ave., Portland, Oregon 97201, United States.
Xiaolin NanKnight Cancer Early Detection Advanced Research Center, Oregon Health & Science University, 2720 S. Moody Ave., Portland, Oregon 97201, United States.ORCID 0000-0002-0597-0255

Funding

Defining mechanisms of Ras clustering and signaling in membrane nanodomains with multiplexed superresolution and correlative microscopiesR01GM132322 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI NAN, XIAOLIN · 2020 to 2023
$1.4M
NIGMS NIH HHS R01 GM132322
6 · The paper itself

Abstract

Metal nanoparticles can be sensitive molecular sensors due to enhanced absorption and scattering of light near a localized surface plasmon resonance (LSPR). Variations in both intrinsic properties such as the geometry and extrinsic properties such as the environment can cause heterogeneity in nanoparticle LSPR and impact the overall sensing responses. To date, however, few studies have examined LSPR and sensing heterogeneities, due to technical challenges in obtaining the full LSPR spectra of individual nanoparticles in dynamic assays. Here, we report multispectral LSPR (msLSPR), a wide-field imaging technique for real-time spectral monitoring of light scattering from individual nanoparticles across the whole field of view (FOV) at ∼0.5 nm spectral and ∼100 ms temporal resolutions. Using msLSPR, we studied the spectral and sensing properties of gold nanoparticles commonly used in LSPR assays, including spheres, rods, and bipyramids. Complemented with electron microscopy imaging, msLSPR analysis revealed that all classes of gold nanoparticles exhibited variations in LSPR peak wavelengths that largely paralleled variations in morphology. Compared with the rods and spheres, gold nanobipyramids exhibited both more uniform and stronger sensing responses as long as the bipyramids are structurally intact. Simulations incorporating the experimental LSPR properties demonstrate the negative impact of spectral heterogeneity on the overall performance of conventional, intensity-based LSPR assays and the ability of msLSPR in overcoming both particle heterogeneity and measurement noise. These results highlight the importance of spectral heterogeneity in LSPR-based sensors and the potential advantage of performing LSPR assays in the spectral domain.

Indexed as

dark-field microscopylocalized surface plasmon resonancemultispectral imagingnanoparticlessingle particle

Identifiers

PMID36660770
PMCPMC9933608

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.