Evidence map›Paper›PMID 28889250›Full record

ReviewPflugers Archiv : European journal of physiology2018

Surface-modified CMOS IC electrochemical sensor array targeting single chromaffin cells for highly parallel amperometry measurements.

Meng Huang, Joannalyn B Delacruz, John C Ruelas, Shailendra S Rathore, Manfred Lindau

Abstract readReview
In one paragraph

Review in Pflugers Archiv : European journal of physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

5 authors.

Meng HuangSchool of Applied and Engineering Physics, Cornell University, Ithaca, NY, 14853, USA.
Joannalyn B DelacruzSchool of Applied and Engineering Physics, Cornell University, Ithaca, NY, 14853, USA.
John C RuelasExoCytronics LLC, 1601 S Providence Rd, Columbia, MO, 65211, USA.
Shailendra S RathoreSchool of Applied and Engineering Physics, Cornell University, Ithaca, NY, 14853, USA.
Manfred LindauSchool of Applied and Engineering Physics, Cornell University, Ithaca, NY, 14853, USA. ml95@cornell.edu.

Funding

Scalable sensor array platform for analysis of quantal transmitter release eventsR01MH095046 · NIMH · CORNELL UNIVERSITY · PI LINDAU, MANFRED · 2011 to 2014
$1.5M
Scalable amperometric microchip array for high-throughput screening of small molecules, peptides or genetic perturbations for modulation of quantal transmitter releaseR43MH109212 · NIMH · EXOCYTRONICS, LLC · PI LINDAU, MANFRED, LIU, XIN ALICE · 2016 to 2017
$869k
NIMH NIH HHS R01 MH095046NIMH NIH HHS R01MH095046NIMH NIH HHS R43 MH109212NIMH NIH HHS R43MH109212
6 · The paper itself

Abstract

Amperometry is a powerful method to record quantal release events from chromaffin cells and is widely used to assess how specific drugs modify quantal size, kinetics of release, and early fusion pore properties. Surface-modified CMOS-based electrochemical sensor arrays allow simultaneous recordings from multiple cells. A reliable, low-cost technique is presented here for efficient targeting of single cells specifically to the electrode sites. An SU-8 microwell structure is patterned on the chip surface to provide insulation for the circuitry as well as cell trapping at the electrode sites. A shifted electrode design is also incorporated to increase the flexibility of the dimension and shape of the microwells. The sensitivity of the electrodes is validated by a dopamine injection experiment. Microwells with dimensions slightly larger than the cells to be trapped ensure excellent single-cell targeting efficiency, increasing the reliability and efficiency for on-chip single-cell amperometry measurements. The surface-modified device was validated with parallel recordings of live chromaffin cells trapped in the microwells. Rapid amperometric spikes with no diffusional broadening were observed, indicating that the trapped and recorded cells were in very close contact with the electrodes. The live cell recording confirms in a single experiment that spike parameters vary significantly from cell to cell but the large number of cells recorded simultaneously provides the statistical significance.

Indexed as

AnimalsChromaffin CellsElectrochemical TechniquesHigh-Throughput Screening AssaysHumansLab-On-A-Chip DevicesMicrochip Analytical ProceduresAmperometryBiosensorCell trappingHigh throughputOn-chip recordingPost-fabricationShift electrode

Identifiers

PMID28889250
PMCPMC5750066

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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.