Evidence map›Paper›PMID 40760197›Full record

ArticleAdvanced biology2025

Spheroid Cell Aggregation Enhanced by Enzyme-Free Ultrasound-Detached Cells.

Julien van Delft, Chikahiro Imashiro, Yuta Kurashina, Makoto Hirano, Jun Homma, Shinsuke Mochizuki, Hideharu Shimozawa, Kenjiro Takemura

Abstract read
In one paragraph

Article in Advanced biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Julien van DelftDepartment of Mechanical Engineering, Keio University, 3-14-1 Hiyoshi Kohoku-ku, Yokohama, 223-8522, Japan.
Chikahiro ImashiroSchool of Engineering, University of Tokyo, Tokyo, 113-8654, Japan.ORCID 0000-0002-0716-2585
Yuta KurashinaDivision of Advanced Mechanical Systems Engineering, Institute of Engineering, Tokyo University of Agriculture and Technology, Tokyo, 184-8588, Japan.ORCID 0000-0003-3752-7204
Makoto HiranoDepartment of Pharmacy, Yasuda Women's University, Hiroshima, 731-0153, Japan.
Jun HommaInstitute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.ORCID 0009-0001-1976-0670
Shinsuke MochizukiMedical Systems and Components Operations, Canon Inc., Tokyo, 146-8501, Japan.ORCID 0009-0005-4116-2246
Hideharu ShimozawaMedical Systems and Components Operations, Canon Inc., Tokyo, 146-8501, Japan.ORCID 0009-0006-5980-8954
Kenjiro TakemuraDepartment of Mechanical Engineering, Keio University, 3-14-1 Hiyoshi Kohoku-ku, Yokohama, 223-8522, Japan.ORCID 0000-0002-0298-5558

Funding

JSPS KAKENHI 23K22661
6 · The paper itself

Abstract

Spheroids are being widely studied as potential building blocks for complex organ engineering, tools for drug screening and cancer study. However, formation time has become the bottleneck of applications due to the need for large-scale high-quality spheroids production. Formation time is often dominated by ECM construction and not cell aggregation. Therefore, this study focuses on the influence of ultrasound detachment replacing conventional enzyme detachment on spheroid formation processes. Thanks to cell surface protein preservation in ultrasound detachment, cell aggregation time is reduced while decreasing the formation variabilities. Moreover, it is confirmed that cells are intrinsically more capable of aggregating through enzyme-free detachment. On top of that, transplantations into rats showed equally successful engraftment properties for enzyme-free detached cells. Finally, the impact on the real co-cultured spheroid application was shown to be beneficial through more localized cell groups inside of the spheroids, possibly improving therapeutic effects and vascularization. Through this study, it is proved that ultrasound detachment can replace enzyme detachment without degrading the final spheroid properties but reducing the formation time, and variability and improving robustness and cell distribution. This opens up a new range of applications for better and faster spheroid formation in numerous bioengineering applications.

Indexed as

Cell AggregationSpheroids, CellularAnimalsCell AdhesionCell Culture TechniquesCoculture TechniquesHumansRatsUltrasonic Waves3D aggregatesenzyme‐freespheroidstissue engineeringultrasound

Identifiers

PMID40760197
PMCPMC12365725

What Socratic 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 Socratic graph.