Evidence map›Paper›PMID 25105251›Full record

ArticleThe Analyst2014

Microfluidic device with tunable post arrays and integrated electrodes for studying cellular release.

Asmira Selimovic, Jayda L Erkal, Dana M Spence, R Scott Martin

Abstract read
In one paragraph

Article in The Analyst, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Insert-based microfluidics for 3D cell culture with analysis.Analytical and bioanalytical chemistry · 2018
    Article
  9. Article
  10. Article
  11. Review
  12. 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.

Asmira SelimovicDepartment of Chemistry, Saint Louis University, 3501 Laclede Ave, St. Louis, MO 63103, USA. martinrs@slu.edu.
Jayda L Erkal
Dana M Spence
R Scott Martin
Michigan State University · USSaint Louis University · US

Funding

Microchip-based Cell Reactor/Analysis SystemR15GM084470 · NIGMS · SAINT LOUIS UNIVERSITY · PI MARTIN, ROBERT SCOTT · 2008 to 2019
$1.3M
Modular Microfluidics as an Enhanced Bioanalytical ToolR21EB016379 · NIBIB · MICHIGAN STATE UNIVERSITY · PI SPENCE, DANA M · 2013 to 2014
$393k
NIBIB NIH HHS R21 EB016379NIBIB NIH HHS R21EB016379-01NIGMS NIH HHS R15 GM084470NIGMS NIH HHS R15GM084470-03
6 · The paper itself

Abstract

In this paper, we describe the development of a planar, pillar array device that can be used to image either side of a tunable membrane, as well as sample and detect small molecules in a cell-free region of the microchip. The pores are created by sealing two parallel PDMS microchannels (a cell channel and a collector channel) over a gold pillar array (5 or 10 μm in height), with the device being characterized and optimized for small molecule cross-over while excluding a flowing cell line (here, red blood cells, RBCs). The device was characterized in terms of the flow rate dependence of analyte cross-over and cell exclusion as well as the ability to perform amperometric detection of catechol and nitric oxide (NO) as they cross-over into the collector channel. Using catechol as the test analyte, the limits of detection (LOD) of the cross-over for the 10 μm and 5 μm pillar array heights were shown to be 50 nM and 105 nM, respectively. Detection of NO was made possible with a glassy carbon detection electrode (housed in the collector channel) modified with Pt-black and Nafion, to enhance sensitivity and selectivity, respectively. Reproducible cross-over of NO as a function of concentration resulted in a linear correlation (r(2) = 0.995, 7.6-190 μM), with an LOD for NO of 230 nM on the glassy carbon/Pt-black/0.05% Nafion electrode. The applicability of the device was demonstrated by measuring the NO released from hypoxic RBCs, with the device allowing the released NO to cross-over into a cell free channel where it was detected in close to real-time. This type of device is an attractive alternative to the use of 3-dimensional devices with polycarbonate membranes, as either side of the membrane can be imaged and facile integration of electrochemical detection is possible.

Indexed as

ElectrodesCatecholsErythrocytesFlow Injection AnalysisHumansLimit of DetectionMicrofluidicsNitric OxidecatecholCatecholsNitric Oxide

Identifiers

PMID25105251
PMCPMC4313528
OpenAlexW2056710781

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.