Evidence map›Paper›PMID 38806765›Full record

ReviewBiomedical microdevices2024

Uniform sized cancer spheroids production using hydrogel-based droplet microfluidics: a review.

Sungjin Kim, Po Yi Lam, Arul Jayaraman, Arum Han

Abstract readReview
In one paragraph

Review in Biomedical microdevices, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
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.

Sungjin KimDepartment of Electrical and Computer Engineering, Texas A&M University, College Station, TX, USA.
Po Yi LamDepartment of Electrical and Computer Engineering, Texas A&M University, College Station, TX, USA.
Arul JayaramanDepartment of Chemical Engineering, Texas A&M University, College Station, TX, USA.
Arum HanDepartment of Electrical and Computer Engineering, Texas A&M University, College Station, TX, USA. arum.han@ece.tamu.edu.

Funding

Single cell, multi-parametric high throughput platform to classify endocrine disruptor potential of mixturesP42ES027704 · NIEHS · TEXAS A&M UNIVERSITY · PI Thomas Joseph McDonald · 2017 to 2026
$21.2M
Advanced Research Projects Agency for Health 1AY1AX000010-01Army Research Office W911NF-19-1-0290Defense Advanced Research Projects Agency W911NF1920013NIEHS NIH HHS P42 ES027704NIEHS NIH HHS P42ES027704
6 · The paper itself

Abstract

Three-dimensional (3D) cell culture models have been extensively utilized in various mechanistic studies as well as for drug development studies as superior in vitro platforms than conventional two-dimensional (2D) cell culture models. This is especially the case in cancer biology, where 3D cancer models, such as spheroids or organoids, have been utilized extensively to understand the mechanisms of cancer development. Recently, many sophisticated 3D models such as organ-on-a-chip models are emerging as advanced in vitro models that can more accurately mimic the in vivo tissue functions. Despite such advancements, spheroids are still considered as a powerful 3D cancer model due to the relatively simple structure and compatibility with existing laboratory instruments, and also can provide orders of magnitude higher throughput than complex in vitro models, an extremely important aspects for drug development. However, creating well-defined spheroids remain challenging, both in terms of throughputs in generation as well as reproducibility in size and shape that can make it challenging for drug testing applications. In the past decades, droplet microfluidics utilizing hydrogels have been highlighted due to their potentials. Importantly, core-shell structured gel droplets can avoid spheroid-to-spheroid adhesion that can cause large variations in assays while also enabling long-term cultivation of spheroids with higher uniformity by protecting the core organoid area from external environment while the outer porous gel layer still allows nutrient exchange. Hence, core-shell gel droplet-based spheroid formation can improve the predictivity and reproducibility of drug screening assays. This review paper will focus on droplet microfluidics-based technologies for cancer spheroid production using various gel materials and structures. In addition, we will discuss emerging technologies that have the potential to advance the production of spheroids, prospects of such technologies, and remaining challenges.

Indexed as

HydrogelsSpheroids, CellularAnimalsCell Culture TechniquesCell Culture Techniques, Three DimensionalHumansLab-On-A-Chip DevicesMicrofluidicsNeoplasmsHydrogels3D cell cultureCancer AggregateCaner SpheroidCore-shell dropletDroplet microfluidicsGel Microdroplet

Identifiers

PMID38806765
PMCPMC11241584

What OpenQuestion holds

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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.