Evidence map›Paper›PMID 28499337›Full record

ArticleAnalytical chemistry2017

Optically Encoded Semiconducting Polymer Dots with Single-Wavelength Excitation for Barcoding and Tracking of Single Cells.

Chun-Ting Kuo, Hong-Shang Peng, Yu Rong, Jiangbo Yu, Wei Sun, Bryant Fujimoto, Daniel T Chiu

Abstract read
In one paragraph

Article in Analytical chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Biomedical optics express · 2022
    Article
  4. Article
  5. Article
  6. Ratiometric Barcoding for Mass Cytometry.Analytical chemistry · 2018
    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.

Chun-Ting KuoDepartment of Chemistry and Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Hong-Shang PengCollege of Science, Minzu University of China , Beijing 100081, China.ORCID 0000-0003-0634-3867
Yu RongDepartment of Chemistry and Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Jiangbo YuDepartment of Chemistry and Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Wei SunDepartment of Chemistry and Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Bryant FujimotoDepartment of Chemistry and Bioengineering, University of Washington , Seattle, Washington 98195, United States.
Daniel T ChiuDepartment of Chemistry and Bioengineering, University of Washington , Seattle, Washington 98195, United States.ORCID 0000-0003-2964-9578

Funding

High-precision mapping of the spatial organization of synaptic-vesicle membrane proteinsR01MH113333 · NIMH · UNIVERSITY OF WASHINGTON · PI CHIU, DANIEL T · 2017 to 2021
$1.9M
Ultra-Bright Probes with Ultra-Narrow Emission for Molecular and Cellular AnalysiR21CA186798 · NCI · UNIVERSITY OF WASHINGTON · PI CHIU, DANIEL T · 2014 to 2016
$672k
NCI NIH HHS R21 CA186798NIMH NIH HHS R01 MH113333
6 · The paper itself

Abstract

Multiplexed optical encoding is emerging as a powerful technique for high-throughput cellular analysis and molecular assays. Most of the developed optical barcodes, however, either suffer from large particle size or are incompatible with most commercial optical instruments. Here, a new type of nanoscale fluorescent barcode (Pdot barcodes) was prepared from semiconducting polymers. The Pdot barcodes possess the merits of small size (∼20 nm in diameter), narrow emission bands (full-width-at-half-maximum (fwhm) of 30-40 nm), three-color emissions (blue, green, and red) under single-wavelength excitation, a high brightness, good pH and thermal stability, and efficient cellular uptake. The Pdot barcodes were prepared using a three-color and six-intensity encoding strategy; for ratiometric readout of the barcodes, one of the colors might be used as an internal reference. We used the Pdot barcodes to label 20 sets of cancer cells and then distinguished and identified each set based on the Pdot barcodes using flow cytometry. We also monitored and tracked single cells labeled with different Pdot barcodes, even through rounds of cell division. These results suggest Pdot barcodes are strong candidates for discriminating different labeled cell and for long-term cell tracking.

Indexed as

Single-Cell AnalysisBoron CompoundsColorFluorenesFluorescent DyesHumansHydrogen-Ion ConcentrationMCF-7 CellsMolecular StructureOptical PhenomenaParticle SizePolymersQuantum DotsSemiconductorsSurface PropertiesTemperature4,4-difluoro-4-bora-3a,4a-diaza-s-indaceneBoron CompoundsfluoreneFluorenesFluorescent DyesPolymers

Identifiers

PMID28499337
PMCPMC5695559

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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.