Evidence map›Paper›PMID 23427919›Full record

ArticleAnalytical chemistry2013

Generating arbitrary chemical patterns for multipoint dosing of single cells.

Todd J Hoppe, Samira G Moorjani, Jason B Shear

Abstract read
In one paragraph

Article in Analytical chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Todd J HoppeDepartment of Chemistry and Biochemistry, The University of Texas at Austin, Austin, Texas 78712-0165, United States.
Samira G Moorjani
Jason B Shear

Funding

Precision Multi-site Cellular Dosing using a Membrane-Based Laminar-Flow DeviceR43MH085396 · NIMH · MINOTAUR TECHNOLOGIES, LLC · PI GOFORTH, ROBYN L · 2009 to 2010
$700k
Subcellular Targeting of Dosant Streams in CultureR21GM078228 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI SHEAR, JASON BEN · 2006 to 2007
$307k
NIGMS NIH HHS R21 GM078228NIMH NIH HHS 1R43MH085396-01NIMH NIH HHS R43 MH085396
6 · The paper itself

Abstract

Living cells reside within anisotropic microenvironments that orchestrate a broad range of polarized responses through physical and chemical cues. To unravel how localized chemical signals influence complex behaviors, tools must be developed for establishing patterns of chemical gradients that vary over subcellular dimensions. Here, we present a strategy for addressing this critical need in which an arbitrary number of chemically distinct, subcellular dosing streams are created in real time within a microfluidic environment. In this approach, cells are cultured on a thin polymer membrane that serves as a barrier between the cell-culture environment and a reagent chamber containing multiple reagent species flowing in parallel under low Reynolds number conditions. Focal ablation of the membrane creates pores that allow solution to flow from desired regions within this reagent pattern into the cell-culture chamber, resulting in narrow, chemically distinct dosing streams. Unlike previous dosing strategies, this system provides the capacity to tailor arbitrary patterns of reagents on the fly to suit the geometry and orientation of specific cells.

Indexed as

AnimalsCell Culture TechniquesCell Line, TumorFluorescent DyesLaser TherapyMicrofluidic Analytical TechniquesMicroscopySingle-Cell AnalysisFluorescent Dyes

Identifiers

PMID23427919
PMCPMC3645469

What OpenQuestion holds

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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.