Evidence map›Paper›PMID 39238893›Full record

ArticleOptica2017

Stimulated Raman scattering flow cytometry for label-free single-particle analysis.

Chi Zhang, Kai-Chih Huang, Bartek Rajwa, Junjie Li, Shiqi Yang, Haonan Lin, Chien-Sheng Liao, Gregory Eakins, Shihuan Kuang, Valery Patsekin and 2 more

Abstract read
In one paragraph

Article in Optica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Article
  2. Review
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  11. Review
  12. Raman cell sorting for single-cell research.Frontiers in bioengineering and biotechnology · 2024
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Toward the Next Frontiers of Vibrational Bioimaging.Chemical & biomedical imaging · 2023
    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

12 authors.

Chi ZhangWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, USA.
Kai-Chih HuangWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, USA.
Bartek RajwaBindley Bioscience Center, Purdue University, West Lafayette, Indiana 47907, USA.
Junjie LiWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, USA.
Shiqi YangDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Haonan LinWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, USA.
Chien-Sheng LiaoWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, USA.
Gregory EakinsDepartment of Chemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Shihuan KuangDepartment of Animal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Valery PatsekinDepartment of Basic Medical Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
J Paul RobinsonWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, USA.
Ji-Xin ChengWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana 47907, USA.

Funding

High-throughput high-content single cell analysis by multichannel stimulatedRaman flow cytometryR01GM118471 · NIGMS · PURDUE UNIVERSITY · PI CHENG, JI-XIN · 2016 to 2019
$1.6M
NIGMS NIH HHS R01 GM118471
6 · The paper itself

Abstract

Flow cytometry is one of the most important technologies for high-throughput single-cell analysis. Fluorescent labeling acts as the primary approach for cellular analysis in flow cytometry. Nevertheless, the fluorescent tags are not applicable to all cases, especially to small molecules, for which labeling may significantly perturb the biological functionality. Spontaneous Raman scattering flow cytometry offers the capability to non-invasively detect chemical contents of cells but suffers from slow data acquisition. In order to achieve label-free high-throughput single-particle analysis using Raman scattering, we developed a 32-channel multiplex stimulated Raman scattering flow cytometry (SRS-FC) technique that can measure chemical contents of single particles at a speed of 5 μs per Raman spectrum. Using mixed polymer beads, we demonstrate the discrimination of different particles at a throughput of up to 11,000 particles per second. This is a four orders of magnitude improvement in throughput compared to conventional spontaneous Raman flow cytometry. As a proof of concept, we show the differentiation of 3T3-L1 cells at different states by SRS-FC according to the difference in cellular chemical content. The SRS-FC technique opens new opportunities for high-throughput and high-content chemical analysis of live cells in a label-free manner.

Indexed as

(120.6200) Spectrometers and spectroscopic instrumentation(170.1530) Cell analysis(170.5660) Raman spectroscopy(290.5910) Scattering, stimulated Raman(300.6420) Spectroscopynonlinear

Identifiers

PMID39238893
PMCPMC11375991

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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.