Evidence map›Paper›PMID 32938987›Full record

ArticleScientific reports2020

Effect of design geometry, exposure energy, cytophilic molecules, cell type and load in fabrication of single-cell arrays using micro-contact printing.

Swapnil Vilas Bhujbal, Maren Dekov, Vegar Ottesen, Karen Dunker, Rahmi Lale, Marit Sletmoen

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Swapnil Vilas Bhujbal *Department of Biotechnology and Food Science, Norwegian University of Science and Technology, 7491, Trondheim, Norway.
Maren Dekov *Department of Biotechnology and Food Science, Norwegian University of Science and Technology, 7491, Trondheim, Norway.
Vegar OttesenDepartment of Chemical Engineering, Norwegian University of Science and Technology, 7491, Trondheim, Norway.
Karen DunkerDepartment of Biotechnology and Food Science, Norwegian University of Science and Technology, 7491, Trondheim, Norway.
Rahmi LaleDepartment of Biotechnology and Food Science, Norwegian University of Science and Technology, 7491, Trondheim, Norway.
Marit SletmoenDepartment of Biotechnology and Food Science, Norwegian University of Science and Technology, 7491, Trondheim, Norway. marit.sletmoen@ntnu.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study a range of factors influencing the fabrication of single-cell arrays (SCAs) are identified and investigated. Micro-contact printing was used to introduce spots coated with polyethyleneimine or Matrigel on glass surfaces pre-coated with polyethylene glycol. Unmodified E. coli, Synechococcus sp., Chlamydomonas reinhardtii as well as diverse mammalian cells including HUVEC, AAV293, U87, OHS, PC3, SW480, HepG2 and AY-27 were successfully immobilised onto the chemically coated spots. The developed SCAs show high cell viability and probability for capturing single-cells. A discrepancy between the size and shape of the squares described in the design file and the actual structures obtained in the final PDMS structure is characterised and quantified. The discrepancy is found to be depending on the exposure energy used in the photolithography process as well as the size of the squares and their separation distance as detailed in the design file. In addition to these factors, the effect of the cell density loaded onto the patterned surfaces is also characterised. The systematic characterisation of key parameters that need to be optimised prior to the fabrication of SCAs is essential in order to increase the efficiency and reproducibility of future fabrication of SCAs for single-cell studies.

Indexed as

Cell SurvivalChlamydomonas reinhardtiiEquipment DesignEscherichia coliHep G2 CellsHumansHuman Umbilical Vein Endothelial CellsPolyethylene GlycolsPolyethyleneiminePrinting, Three-DimensionalSingle-Cell AnalysisSurface PropertiesSynechococcusPolyethylene GlycolsPolyethyleneimine

Identifiers

PMID32938987
PMCPMC7494944

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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.