Evidence map›Paper›PMID 27990542›Full record

ArticleLab on a chip2017

3D-templated, fully automated microfluidic input/output multiplexer for endocrine tissue culture and secretion sampling.

Xiangpeng Li, Jessica C Brooks, Juan Hu, Katarena I Ford, Christopher J Easley

Abstract read
In one paragraph

Article in Lab on a chip, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
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  3. Dynamic sampling fromLab on a chip · 2024
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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.

Xiangpeng LiDepartment of Chemistry and Biochemistry, Auburn University, Auburn, AL 36849, USA. chris.easley@auburn.edu.
Jessica C BrooksDepartment of Chemistry and Biochemistry, Auburn University, Auburn, AL 36849, USA. chris.easley@auburn.edu.
Juan HuDepartment of Chemistry and Biochemistry, Auburn University, Auburn, AL 36849, USA. chris.easley@auburn.edu.
Katarena I FordDepartment of Chemistry and Biochemistry, Auburn University, Auburn, AL 36849, USA. chris.easley@auburn.edu.
Christopher J EasleyDepartment of Chemistry and Biochemistry, Auburn University, Auburn, AL 36849, USA. chris.easley@auburn.edu.ORCID 0000-0002-2403-4147

Funding

Unmasking mechanisms of lipolytic dynamics in adipose tissue using high-resolution microfluidic samplingR01DK093810 · NIDDK · AUBURN UNIVERSITY AT AUBURN · PI EASLEY, CHRISTOPHER J · 2012 to 2023
$3.8M
NIDDK NIH HHS R01 DK093810
6 · The paper itself

Abstract

A fully automated, 16-channel microfluidic input/output multiplexer (μMUX) has been developed for interfacing to primary cells and to improve understanding of the dynamics of endocrine tissue function. The device utilizes pressure driven push-up valves for precise manipulation of nutrient input and hormone output dynamics, allowing time resolved interrogation of the cells. The ability to alternate any of the 16 channels from input to output, and vice versa, provides for high experimental flexibility without the need to alter microchannel designs. 3D-printed interface templates were custom designed to sculpt the above-channel polydimethylsiloxane (PDMS) in microdevices, creating millimeter scale reservoirs and confinement chambers to interface primary murine islets and adipose tissue explants to the μMUX sampling channels. This μMUX device and control system was first programmed for dynamic studies of pancreatic islet function to collect ∼90 minute insulin secretion profiles from groups of ∼10 islets. The automated system was also operated in temporal stimulation and cell imaging mode. Adipose tissue explants were exposed to a temporal mimic of post-prandial insulin and glucose levels, while simultaneous switching between labeled and unlabeled free fatty acid permitted fluorescent imaging of fatty acid uptake dynamics in real time over a ∼2.5 hour period. Application with varying stimulation and sampling modes on multiple murine tissue types highlights the inherent flexibility of this novel, 3D-templated μMUX device. The tissue culture reservoirs and μMUX control components presented herein should be adaptable as individual modules in other microfluidic systems, such as organ-on-a-chip devices, and should be translatable to different tissues such as liver, heart, skeletal muscle, and others.

Indexed as

Lab-On-A-Chip DevicesAdipose TissueAnimalsAutomationEquipment DesignIslets of LangerhansMaleMiceMice, Inbred C57BLTissue Culture Techniques

Identifiers

PMID27990542
PMCPMC5293597

What OpenQuestion holds

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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.