Evidence map›Paper›PMID 30421505›Full record

ArticleJournal of biophotonics2019

Integration of diffraction phase microscopy and Raman imaging for label-free morpho-molecular assessment of live cells.

Rishikesh Pandey, Renjie Zhou, Rosalie Bordett, Ciera Hunter, Kristine Glunde, Ishan Barman, Tulio Valdez, Christine Finck

Abstract read
In one paragraph

Article in Journal of biophotonics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Quantitative phase microscopies: accuracy comparison.Light, science & applications · 2024
    Review
  4. Article
  5. Injectable amnion hydrogel-mediated delivery of adipose-derived stem cells for osteoarthritis treatment.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Article
  7. Article
  8. 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

8 authors.

Rishikesh PandeyConnecticut Children's Innovation Center, University of Connecticut School of Medicine, Farmington, Connecticut.ORCID 0000-0003-4975-3815
Renjie ZhouDepartment of Chemistry, Laser Biomedical Research Center, George R. Harrison Spectroscopy Lab, Massachusetts Institute of Technology, Cambridge, Massachusetts.ORCID 0000-0002-4761-6641
Rosalie BordettConnecticut Children's Innovation Center, University of Connecticut School of Medicine, Farmington, Connecticut.
Ciera HunterConnecticut Children's Innovation Center, University of Connecticut School of Medicine, Farmington, Connecticut.
Kristine GlundeThe Johns Hopkins University School of Medicine, The Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland.
Ishan BarmanThe Johns Hopkins University School of Medicine, The Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland.ORCID 0000-0003-0800-0825
Tulio ValdezDepartment of Otolaryngology, Stanford University, Palo Alto, California.
Christine FinckConnecticut Children's Innovation Center, University of Connecticut School of Medicine, Farmington, Connecticut.

Funding

Wide-Field Short-Wave Infrared (SWIR) multiphoton (MP) tissue imagingP41EB015871 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2012 to 2021
$11.3M
Spectroscopy assisted mechano-chemical phenotype recognition nanoscopeDP2GM128198 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI BARMAN, ISHAN · 2017 to 2017
$2.5M
Connecticut Children's Innovation Center Seed Money; National Institute of Biomedical Imaging and Bioengineering 2-P41-EB015871-31NIBIB NIH HHS P41 EB015871NIGMS NIH HHS DP2 GM128198NIGMS NIH HHS DP2GM128198The Chinese University of Hong Kong Direct Research Grant; Shun Hing Institute of Advanced Engineering BME-p3-18
6 · The paper itself

Abstract

Label-free quantitative imaging is highly desirable for studying live cells by extracting pathophysiological information without perturbing cell functions. Here, we demonstrate a novel label-free multimodal optical imaging system with the capability of providing comprehensive morphological and molecular attributes of live cells. Our morpho-molecular microscopy (3M) system draws on the combined strength of quantitative phase microscopy (QPM) and Raman microscopy to probe the morphological features and molecular fingerprinting characteristics of each cell under observation. While the commonr-path geometry of our QPM system allows for highly sensitive phase measurement, the Raman microscopy is equipped with dual excitation wavelengths and utilizes the same detection and dispersion system, making it a distinctive multi-wavelength system with a small footprint. We demonstrate the applicability of the 3M system by investigating nucleated and nonnucleated cells. This integrated label-free platform has a promising potential in preclinical research, as well as in clinical diagnosis in the near future.

Indexed as

Cell Line, TumorCell SurvivalHumansMicroscopySpectrum Analysis, Ramancellular imaginglabel-free imagingquantitative phase microscopyRaman spectroscopy

Identifiers

PMID30421505
PMCPMC6447451

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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.