Evidence map›Paper›PMID 27571395›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2016

Multiplexed Molecular Imaging of Fresh Tissue Surfaces Enabled by Convection-Enhanced Topical Staining with SERS-Coded Nanoparticles.

Yu W Wang, Josh D Doerksen, Soyoung Kang, Daniel Walsh, Qian Yang, Daniel Hong, Jonathan T C Liu

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
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

38 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
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  6. Article
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  9. Review
  10. Multiplexed imaging in oncology.Nature biomedical engineering · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Cancer Diagnosis through SERS and Other Related Techniques.International journal of molecular sciences · 2020
    Review
  18. Article
  19. Review
  20. 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 at 2 institutions in 2 countries.

Yu W WangDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98195, USA. yuwang2@uw.edu.
Josh D DoerksenDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98195, USA.
Soyoung KangDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98195, USA.
Daniel WalshDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98195, USA.
Qian YangDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98195, USA.
Daniel HongDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98195, USA.
Jonathan T C LiuDepartment of Mechanical Engineering, University of Washington, Seattle, WA, 98195, USA. jonliu@uw.edu.
University of Washington · USChengdu Medical College · CN

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Endoscopic molecular imaging of esophageal cancer with multiplexed Raman nanopartR21EB015016 · NIBIB · UNIVERSITY OF WASHINGTON · PI LIU, JONATHAN T.C. · 2013 to 2014
$493k
NCI NIH HHS P30 CA015704NIBIB NIH HHS R21 EB015016
6 · The paper itself

Abstract

There is a need for intraoperative imaging technologies to guide breast-conserving surgeries and to reduce the high rates of re-excision for patients in which residual tumor is found at the surgical margins during postoperative pathology analyses. Feasibility studies have shown that utilizing topically applied surface-enhanced Raman scattering (SERS) nanoparticles (NPs), in conjunction with the ratiometric imaging of targeted versus untargeted NPs, enables the rapid visualization of multiple cell-surface biomarkers of cancer that are overexpressed at the surfaces of freshly excised breast tissues. In order to reliably and rapidly perform multiplexed Raman-encoded molecular imaging of large numbers of biomarkers (with five or more NP flavors), an enhanced staining method has been developed in which tissue surfaces are cyclically dipped into an NP-staining solution and subjected to high-frequency mechanical vibration. This dipping and mechanical vibration (DMV) method promotes the convection of the SERS NPs at fresh tissue surfaces, which accelerates their binding to their respective biomarker targets. By utilizing a custom-developed device for automated DMV staining, this study demonstrates the ability to simultaneously image four cell-surface biomarkers of cancer at the surfaces of fresh human breast tissues with a mixture of five flavors of SERS NPs (four targeted and one untargeted control) topically applied for 5 min and imaged at a spatial resolution of 0.5 mm and a raster-scanned imaging rate of >5 cm

Indexed as

ConvectionStaining and Labeling3T3 CellsAnimalsBreastCell Line, TumorFemaleHumansMiceMice, NudeMolecular ImagingNanoparticlesReproducibility of ResultsSpectrum Analysis, RamanSurface PropertiesXenograft Model Antitumor Assaysbiomedical optical imagingcancer detectionmolecular imagingnanomedicineRaman spectroscopy

Identifiers

PMID27571395
PMCPMC5462459
OpenAlexW2508492654

What OpenQuestion holds

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Read underepoch 390

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.