Evidence map›Paper›PMID 27245782›Full record

ArticleScientific reports2016

A neuron-in-capillary platform for facile collection and mass spectrometric characterization of a secreted neuropeptide.

Chang Young Lee, Yi Fan, Stanislav S Rubakhin, Sook Yoon, Jonathan V Sweedler

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Cell Analysis on Microfluidics Combined with Mass Spectrometry.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2021
    Review
  3. Review
  4. Review
  5. Single Cell Neurometabolomics.ACS chemical neuroscience · 2018
    Review
  6. Article
  7. Review
  8. 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

5 authors at 2 institutions in 2 countries.

Chang Young LeeDepartment of Chemistry and the Beckman Institute, University of Illinois, Urbana, IL 61801, USA.
Yi FanDepartment of Chemistry and the Beckman Institute, University of Illinois, Urbana, IL 61801, USA.
Stanislav S RubakhinDepartment of Chemistry and the Beckman Institute, University of Illinois, Urbana, IL 61801, USA.
Sook YoonSchool of Energy and Chemical Engineering, School of Life Sciences, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.
Jonathan V SweedlerDepartment of Chemistry and the Beckman Institute, University of Illinois, Urbana, IL 61801, USA.
University of Illinois Urbana-Champaign · USUlsan National Institute of Science and Technology · KR

Funding

The UIUC Neuroproteomics Center on Cell-Cell SignalingP30DA018310 · NIDA · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI Elena V Romanova · 2004 to 2026
$24.9M
The National Resource for Aplysia-Curation & Informatics.P40OD010952 · OD · UNIVERSITY OF MIAMI ROSENTEIL SCHOOL · PI M Danielle McDonald · 2012 to 2026
$10.7M
NIDA NIH HHS P30 DA018310NIH HHS P40 OD010952
6 · The paper itself

Abstract

The integration of microfluidic devices-which efficiently handle small liquid volumes-with separations/mass spectrometry (MS) is an effective approach for profiling the neurochemistry occurring in selected neurons. Interfacing the microfluidic cell culture to the mass spectrometer is challenging because of geometric and scaling issues. Here we demonstrate the hyphenation of a neuron-in-capillary platform to a solid phase extraction device and off-line MS. A primary neuronal culture of Aplysia californica neurons was established directly inside a cylindrical polyimide capillary. The approach also uses a particle-embedded monolith to condition neuropeptide releasates collected from several Aplysia neurons cultured in the capillary, with the subsequent characterization of released peptides via MS. This system presents a number of advances compared to more traditional microfluidic devices fabricated with polydimethylsiloxane. These include low cost, easy access to cell culture, rigidity, ease of transport, and minimal fluid handling. The cylindrical geometry of the platform allows convenient interface with a wide range of analytical tools that utilize capillary columns.

Indexed as

AnimalsAplysiaCell Culture TechniquesDimethylpolysiloxanesLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesNeuronsNeuropeptidesPotassium ChloridePrimary Cell CultureResins, SyntheticSolid Phase ExtractionSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationbaysilonDimethylpolysiloxanesNeuropeptidespolyimide resinPotassium ChlorideResins, Synthetic

Identifiers

PMID27245782
PMCPMC4887886
OpenAlexW2493673247

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.