Evidence map›Paper›PMID 26250488›Full record

ArticleJournal of biomolecular screening2015

Magnetic Alignment of Microelements Containing Cultured Neuronal Networks for High-Throughput Screening.

Kent R Gordon, Yuli Wang, Nancy L Allbritton, Anne Marion Taylor

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomolecular screening, 2015. 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
0.1field-weighted citation impact, top 54% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  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

4 authors at 2 institutions in 1 country.

Kent R GordonUNC/NCSU Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Chapel Hill and Raleigh, NC.
Yuli WangDepartment of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Nancy L AllbrittonUNC/NCSU Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Chapel Hill and Raleigh, NC Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Anne Marion TaylorUNC/NCSU Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Chapel Hill and Raleigh, NC Neuroscience Center, University of North Carolina at Chapel Hill, Chapel Hill, NC Carolina Institute for Developmental Disabilities, Carrboro, NC amtaylor@unc.edu.
North Carolina State University · USUniversity of North Carolina at Chapel Hill · US

Funding

UNC Neuroscience Center Research Cores: MicroscopyP30NS045892 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ZYLKA, MARK J. · 2003 to 2022
$11.5M
Generation of a Gene-Targeted Human iPS Cell Library for Macular DegenerationR01EY024556 · NEI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ALLBRITTON, NANCY L. · 2014 to 2018
$2.9M
A user-friendly scalable microfluidic platform for enhanced neuron-cell cultureR42MH097377 · NIMH · XONA MICROFLUIDICS, LLC · PI TAYLOR, ANNE MARION · 2016 to 2018
$2.0M
A user-friendly scalable microfluidic platform for enhanced neuron-cell cultureR41MH097377 · NIMH · XONA MICROFLUIDICS, LLC · PI TAYLOR, ANNE MARION · 2013 to 2014
$679k
NEI NIH HHS R01 EY024556NEI NIH HHS R01EY024556NIMH NIH HHS R41 MH097377NIMH NIH HHS R41MH097377NIMH NIH HHS R42 MH097377NINDS NIH HHS P30 NS045892
6 · The paper itself

Abstract

High-throughput screening (HTS) on neurons presents unique difficulties because they are postmitotic, limited in supply, and challenging to harvest from animals or generate from stem cells. These limitations have hindered neurological drug discovery, leaving an unmet need to develop cost-effective technology for HTS using neurons. Traditional screening methods use up to 20,000 neurons per well in 384-well plates. To increase throughput, we use "microraft" arrays, consisting of 1600 square, releasable, paramagnetic, polystyrene microelements (microrafts), each providing a culture surface for 500-700 neurons. These microrafts can be detached from the array and transferred to 384-well plates for HTS; however, they must be centered within wells for automated imaging. Here, we developed a magnet array plate, compatible with HTS fluid-handling systems, to center microrafts within wells. We used finite element analysis to select an effective size of the magnets and confirmed that adjacent magnetic fields do not interfere. We then experimentally tested the plate's centering ability and found a centering efficiency of 100%, compared with 4.35% using a flat magnet. We concluded that microrafts could be centered after settling randomly within the well, overcoming friction, and confirmed these results by centering microrafts containing hippocampal neurons cultured for 8 days.

Indexed as

AnimalsCells, CulturedCell SurvivalDrug Evaluation, PreclinicalHigh-Throughput Screening AssaysMagnetic PhenomenaNerve NetNeuronsRats, Sprague-Dawleyfinite element analysishigh-throughput screeningmagnetic centeringmicrofabricationmicroraft arraysprimary neurons

Identifiers

PMID26250488
PMCPMC4852856
OpenAlexW1610655214

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.