Evidence map›Paper›PMID 40653897›Full record

ArticleAdvanced healthcare materials2025

Thermoresponsive BrushGel Microcarriers for Efficient Cell Expansion and Enzyme-Reduced Harvesting.

Esfandyar Askari, Mahdieh Shokrollahi Barough, Amir Seyfoori, Mahmood Razzaghi, Joel Alexander Ninan, Aidan B P Murray, Mahmoud Salkhordeh, Yuan Tan, Shirley H J Mei, Mohsen Akbari

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

10 authors.

Esfandyar AskariLaboratory for Innovations in Micro Engineering (LiME), Department of Mechanical Engineering, Victoria, BC, V8P 5C2, Canada.
Mahdieh Shokrollahi BaroughLaboratory for Innovations in Micro Engineering (LiME), Department of Mechanical Engineering, Victoria, BC, V8P 5C2, Canada.
Amir SeyfooriLaboratory for Innovations in Micro Engineering (LiME), Department of Mechanical Engineering, Victoria, BC, V8P 5C2, Canada.
Mahmood RazzaghiLaboratory for Innovations in Micro Engineering (LiME), Department of Mechanical Engineering, Victoria, BC, V8P 5C2, Canada.
Joel Alexander NinanLaboratory for Innovations in Micro Engineering (LiME), Department of Mechanical Engineering, Victoria, BC, V8P 5C2, Canada.
Aidan B P MurrayRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON, K1H 8L6, Canada.
Mahmoud SalkhordehRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON, K1H 8L6, Canada.
Yuan TanRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON, K1H 8L6, Canada.
Shirley H J MeiRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON, K1H 8L6, Canada.
Mohsen AkbariLaboratory for Innovations in Micro Engineering (LiME), Department of Mechanical Engineering, Victoria, BC, V8P 5C2, Canada.ORCID https://orcid.org/0000-0003-2902-6557

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scaling up cell therapy requires efficient expansion of high-quality cells. Microcarrier(MC)-based systems offer high surface-to-volume ratios and reduce culture media usage. In this study, we developed BrushGel, a temperature-responsive MC composed of gelatin methacryloyl (GelMA) hydrogel particles coated with poly(N-isopropyl acrylamide) (PNIPAM) polymer brushes via covalent grafting. BrushGel was fabricated using a flow-focusing droplet microfluidic device and functionalized using carbodiimide chemistry ( 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide-N-Hydroxysuccinimide, EDC-NHS). The degree of PNIPAM coating was tuned by varying the degree of methacrylation (DOM) of GelMA and the concentration of PNIPAM. Human dermal fibroblast (HNDF) cells cultured on the BrushGel under dynamic conditions showed a 4.9 fold increase in cell density, 12-fold upregulation in COL1A1 gene expression and elevated procollagen protein secretion compared to static culture. Low temperature detachment (4 °C) yeilded up to 65% detachment efficiency with >95% post-detachment viability. Clinical grade human bone marrow-derived mesenchymal stromal/stem cells (MSCs) expnaded 5.3 fold over five days on BrushGel with 69% detachment efficiency and 80% post-harvest viability using 10-fold less enzyme. BrushGel supported over 10 days of culture in spinner flasks, enabling enzyme-minimized, scalable cell expansion.  These findings position BrushGel as a promising platfrom for dyanmic cell culture systems in regenerative medicine.

Indexed as

Cell Culture TechniquesHydrogelsAcrylic ResinsCell ProliferationCells, CulturedCollagen Type IFibroblastsGelatinHumansMethacrylatesTemperatureAcrylic ResinsCollagen Type IGelatingelatin methacryloylHydrogelsMethacrylatespoly-N-isopropylacrylamidecell expansiondynamic culturemesenchymal stem cellmicrocarriertemperature‐responsive

Identifiers

PMID40653897
PMCPMC12417781

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.