Evidence map›Paper›PMID 23917952›Full record

ArticleLab on a chip2013

A contact line pinning based microfluidic platform for modelling physiological flows.

Chih-kuan Tung, Oleh Krupa, Elif Apaydin, Jr-Jiun Liou, Anthony Diaz-Santana, Beum Jun Kim, Mingming Wu

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Open Microfluidic Capillary Systems.Analytical chemistry · 2019
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Technology advancement for integrative stem cell analyses.Tissue engineering. Part B, Reviews · 2014
    Review
  15. Modeling tumor microenvironments in vitro.Journal of biomechanical engineering · 2014
    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

7 authors at 1 institution in 1 country.

Chih-kuan TungDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY, USA. ct348@cornell.edu mw272@cornell.edu.
Oleh Krupa
Elif Apaydin
Jr-Jiun Liou
Anthony Diaz-Santana
Beum Jun Kim
Mingming Wu
Cornell University · US

Funding

TRANS-NETWORK PROJECTSU54CA143876 · NCI · CORNELL UNIVERSITY · PI SHULER, MICHAEL L · 2009 to 2014
$12.6M
A 3D microfluidic platform for quantitative assessments of tumor cell migrationR21CA138366 · NCI · CORNELL UNIVERSITY · PI WU, MINGMING · 2010 to 2011
$347k
NCI NIH HHS R21 CA138366NCI NIH HHS R21CA138366NCI NIH HHS U54 CA143876NCI NIH HHS U54CA143876
6 · The paper itself

Abstract

This work introduces a contact line pinning based microfluidic platform for the generation of interstitial and intramural flows within a three dimensional (3D) microenvironment for cellular behaviour studies. A contact line pinning method was used to confine a natively derived biomatrix, collagen, in microfluidic channels without walls. By patterning collagen in designated wall-less channels, we demonstrated and validated the intramural flows through a microfluidic channel bounded by a monolayer of endothelial cells (mimic of a vascular vessel), as well as slow interstitial flows within a cell laden collagen matrix using the same microfluidic platform. The contact line pinning method ensured the generation of an engineered endothelial tube with straight walls, and spatially uniform interstitial fluid flows through the cell embedded 3D collagen matrix. Using this device, we demonstrated that the breast tumour cells' (MDA-MB-231 cell line) morphology and motility were modulated by the interstitial flows, and the motility of a sub-population of the cells was enhanced by the presence of the flow. The presented microfluidic platform provides a basic framework for studies of cellular behaviour including cell transmigration, growth, and adhesion under well controlled interstitial and intramural flows, and within a physiologically realistic 3D co-culture setting.

Indexed as

Cellular MicroenvironmentModels, BiologicalCell Line, TumorCollagenDimethylpolysiloxanesHumansHuman Umbilical Vein Endothelial CellsMicrofluidic Analytical TechniquesbaysilonCollagenDimethylpolysiloxanes

Identifiers

PMID23917952
PMCPMC4505921
OpenAlexW2069829549

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.