Evidence map›Paper›PMID 23044636›Full record

ArticleLab on a chip2012

Time encoded multicolor fluorescence detection in a microfluidic flow cytometer.

Joerg Martini, Michael I Recht, Malte Huck, Marshall W Bern, Noble M Johnson, Peter Kiesel

Abstract read
In one paragraph

Article in Lab on a chip, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Free-Space Excitation of Optofluidic Devices for Pattern-Based Single Particle Detection.IEEE photonics technology letters : a publication of the IEEE Laser and Electro-optics Society · 2021
    Article
  3. Mobile platform for rapid sub-picogram-per-milliliter, multiplexed, digital droplet detection of proteins.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  4. Cell Cytometry: Review and Perspective on Biotechnological Advances.Frontiers in bioengineering and biotechnology · 2019
    Review
  5. Optofluidic bioanalysis: fundamentals and applications.Nanophotonics (Berlin, Germany) · 2017
    Article
  6. Article
  7. Optofluidic wavelength division multiplexing for single-virus detection.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  8. Article
  9. Article
  10. Review
  11. Signal-to-noise Enhancement in Optical Detection of Single Viruses with Multi-spot Excitation.IEEE journal of selected topics in quantum electronics : a publication of the IEEE Lasers and Electro-optics Society
    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

6 authors.

Joerg MartiniPalo Alto Research Center, 3333 Coyote Hill Rd., Palo Alto, CA 94304, USA. joerg.martini@parc.com
Michael I Recht
Malte Huck
Marshall W Bern
Noble M Johnson
Peter Kiesel

Funding

Compact high-performance microfluidic-based flow cytometerR21EB011662 · NIBIB · PALO ALTO RESEARCH CENTER · PI KIESEL, PETER · 2010 to 2011
$492k
NIBIB NIH HHS 5R21EB011662-02NIBIB NIH HHS R21 EB011662
6 · The paper itself

Abstract

We describe an optical detection technique that delivers high signal-to-noise discrimination to enable a multi-parameter flow cytometer that combines high performance, robustness, compactness and low cost. The enabling technique is termed "spatially modulated detection" and generates a time-dependent signal as a continuously fluorescing (bio-) particle traverses an optical transmission pattern along the fluidic channel. Correlating the detected signal with the expected transmission pattern achieves high discrimination of the particle signal from background noise. Additionally, the particle speed and its fluorescence emission characteristics are deduced from the correlation analysis. Our method uses a large excitation/emission volume along the fluidic channel in order to increase the total flux of fluorescence light that originates from a particle while requiring minimal optical alignment. Despite the large excitation/detection volume, the mask pattern enables a high spatial resolution in the micron range. This allows for detection and characterization of particles with a separation (in flow direction) comparable to the dimension of individual particles. In addition, the concept is intrinsically tolerant of non-encoded background fluorescence originating from fluorescent components in solution, fluorescing components of the chamber and contaminants on its surface. The optical detection technique is illustrated with experimental results of multicolor detection with a single large area detector by filtering fluorescence emission of different particles through a patterned color mask. Thereby the particles' fluorescence emission spectrum is encoded in a time dependent intensity signal and color information can be extracted from the correlation analysis. The multicolor detection technique is demonstrated by differentiation of micro-beads loaded with PE (Phycoerythrin) and PE-Cy5 that are excited at 532 nm.

Indexed as

CarbocyaninesColorFlow CytometryFluorescent DyesMicrofluidic Analytical TechniquesPhycoerythrinSpectrometry, FluorescenceTime FactorsCarbocyaninescyanine dye 5Fluorescent DyesPhycoerythrin

Identifiers

PMID23044636
PMCPMC3485422

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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.