Evidence map›Paper›PMID 37438409›Full record

ArticleScientific reports2023

OrganoidChip facilitates hydrogel-free immobilization for fast and blur-free imaging of organoids.

Khashayar Moshksayan, Anirudha Harihara, Sudip Mondal, Evan Hegarty, Todd Atherly, Dipak K Sahoo, Albert E Jergens, Jonathan P Mochel, Karin Allenspach, Janet Zoldan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 16 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Khashayar Moshksayan *Department of Mechanical Engineering, University of Texas at Austin, Austin, TX, USA.
Anirudha Harihara *Department of Mechanical Engineering, University of Texas at Austin, Austin, TX, USA.
Sudip MondalDepartment of Mechanical Engineering, University of Texas at Austin, Austin, TX, USA.
Evan HegartyDepartment of Mechanical Engineering, University of Texas at Austin, Austin, TX, USA.
Todd AtherlyDepartment of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Dipak K SahooDepartment of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Albert E JergensDepartment of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Jonathan P MochelDepartment of Biomedical Sciences, Iowa State University, Ames, IA, USA.
Karin AllenspachDepartment of Veterinary Clinical Sciences, Iowa State University, Ames, IA, USA.
Janet ZoldanDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX, USA.
Adela Ben-YakarDepartment of Mechanical Engineering, University of Texas at Austin, Austin, TX, USA. ben-yakar@mail.utexas.edu.
The University of Texas at Austin · USIowa State University · US

Funding

A Large-Scale Microfluidics Imaging Platform for High-Throughput Toxicity Testing using Canine Intestinal OrganoidsR43ES029890 · NIEHS · VIVOVERSE, LLC · PI HEGARTY, EVAN · 2019 to 2019
$223k
NIEHS NIH HHS R43 ES029890
6 · The paper itself

Abstract

Organoids are three-dimensional structures of self-assembled cell aggregates that mimic anatomical features of in vivo organs and can serve as in vitro miniaturized organ models for drug testing. The most efficient way of studying drug toxicity and efficacy requires high-resolution imaging of a large number of organoids acquired in the least amount of time. Currently missing are suitable platforms capable of fast-paced high-content imaging of organoids. To address this knowledge gap, we present the OrganoidChip, a microfluidic imaging platform that incorporates a unique design to immobilize organoids for endpoint, fast imaging. The chip contains six parallel trapping areas, each having a staging and immobilization chamber, that receives organoids transferred from their native culture plates and anchors them, respectively. We first demonstrate that the OrganoidChip can efficiently immobilize intestinal and cardiac organoids without compromising their viability and functionality. Next, we show the capability of our device in assessing the dose-dependent responses of organoids' viability and spontaneous contraction properties to Doxorubicin treatment and obtaining results that are similar to off-chip experiments. Importantly, the chip enables organoid imaging at speeds that are an order of magnitude faster than conventional imaging platforms and prevents the acquisition of blurry images caused by organoid drifting, swimming, and fast stage movements. Taken together, the OrganoidChip is a promising microfluidic platform that can serve as a building block for a multiwell plate format that can provide high-throughput and high-resolution imaging of organoids in the future.

Indexed as

Bone PlatesHydrogelsDiagnostic ImagingDoxorubicinOrganoidsDoxorubicinHydrogels

Identifiers

PMID37438409
PMCPMC10338466
OpenAlexW4384023930

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.