Evidence map›Paper›PMID 33532812›Full record

ArticleLab on a chip2021

Self-aligned sequential lateral field non-uniformities over channel depth for high throughput dielectrophoretic cell deflection.

XuHai Huang, Karina Torres-Castro, Walter Varhue, Armita Salahi, Ahmed Rasin, Carlos Honrado, Audrey Brown, Jennifer Guler, Nathan S Swami

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Tutorial on Lateral Dielectrophoretic Manipulations in Microfluidic Systems.IEEE transactions on biomedical circuits and systems · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. 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

9 authors at 1 institution in 1 country.

XuHai HuangElectrical & Computer Engineering, University of Virginia, Charlottesville, USA. nswami@virginia.edu.
Karina Torres-CastroElectrical & Computer Engineering, University of Virginia, Charlottesville, USA. nswami@virginia.edu.ORCID 0000-0001-9959-6040
Walter VarhueElectrical & Computer Engineering, University of Virginia, Charlottesville, USA. nswami@virginia.edu.
Armita SalahiElectrical & Computer Engineering, University of Virginia, Charlottesville, USA. nswami@virginia.edu.
Ahmed RasinElectrical & Computer Engineering, University of Virginia, Charlottesville, USA. nswami@virginia.edu.ORCID 0000-0002-7279-3762
Carlos HonradoElectrical & Computer Engineering, University of Virginia, Charlottesville, USA. nswami@virginia.edu.ORCID 0000-0002-4151-2147
Audrey BrownBiology, University of Virginia, Charlottesville, USA.
Jennifer GulerBiology, University of Virginia, Charlottesville, USA.
Nathan S SwamiElectrical & Computer Engineering, University of Virginia, Charlottesville, USA. nswami@virginia.edu and Chemistry, University of Virginia, Charlottesville, USA.ORCID 0000-0002-0492-1160
Charlottesville Medical Research · US

Funding

The integrated Translational Health Research Institute of Virginia (iTHRIV): Using Data to Improve HealthUL1TR003015 · NCATS · UNIVERSITY OF VIRGINIA · PI BROWN, DONALD E, JOHNSTON, KAREN C. · 2019 to 2023
$20.3M
Training in Cell and Molecular BiologyT32GM139787 · NIGMS · UNIVERSITY OF VIRGINIA · PI Bryce Paschal · 2021 to 2026
$2.5M
Optimizing Inter-Microbial Antagonisms to Control Clostridium Difficile InfectionR21AI130902 · NIAID · UNIVERSITY OF VIRGINIA · PI SWAMI, NATHAN, WARREN, CIRLE ALCANTARA · 2017 to 2018
$413k
NCATS NIH HHS UL1 TR003015NIAID NIH HHS R21 AI130902NIGMS NIH HHS T32 GM139787
6 · The paper itself

Abstract

Dielectrophoresis (DEP) enables the separation of cells based on subtle subcellular phenotypic differences by controlling the frequency of the applied field. However, current electrode-based geometries extend over a limited depth of the sample channel, thereby reducing the throughput of the manipulated sample (sub-μL min-1 flow rates and <105 cells per mL). We present a flow through device with self-aligned sequential field non-uniformities extending laterally across the sample channel width (100 μm) that are created by metal patterned over the entire depth (50 μm) of the sample channel sidewall using a single lithography step. This enables single-cell streamlines to undergo progressive DEP deflection with minimal dependence on the cell starting position, its orientation versus the field and intercellular interactions. Phenotype-specific cell separation is validated (>μL min-1 flow and >106 cells per mL) using heterogeneous samples of healthy and glutaraldehyde-fixed red blood cells, with single-cell impedance cytometry showing that the DEP collected fractions are intact and exhibit electrical opacity differences consistent with their capacitance-based DEP crossover frequency. This geometry can address the vision of an "all electric" selective cell isolation and cytometry system for quantifying phenotypic heterogeneity of cellular systems.

Indexed as

Microfluidic Analytical TechniquesCell SeparationElectric ImpedanceElectrodesElectrophoresis

Identifiers

PMID33532812
PMCPMC8019514
OpenAlexW3125611473

What OpenQuestion holds

Textmetadata
LicenceTDM
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.