Evidence map›Paper›PMID 25113941›Full record

ArticleMacromolecular rapid communications2014

Cell-friendly inverse opal-like hydrogels for a spatially separated co-culture system.

Jaeyun Kim, Sidi A Bencherif, Weiwei Aileen Li, David J Mooney

Abstract read
In one paragraph

Article in Macromolecular rapid communications, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Mitigating Metal-Organic Framework (MOF) Toxicity for Biomedical Applications.Chemical engineering journal (Lausanne, Switzerland : 1996) · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Latest Advances in 3D Bioprinting of Cardiac Tissues.Advanced materials technologies · 2022
    Article
  10. Article
  11. Article
  12. Reversed-engineered human alveolar lung-on-a-chip model.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

4 authors.

Jaeyun KimSchool of Chemical Engineering, Sungkyunkwan University, Suwon, 440-746, Republic of Korea; School of Engineering and Applied Sciences and Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, 01238, USA.
Sidi A Bencherif
Weiwei Aileen Li
David J Mooney

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008152 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ARDEHALI, HOSSEIN · 1987 to 2021
$24.0M
Biomaterial based breast cancer vaccineR01EB015498 · NIBIB · HARVARD MEDICAL SCHOOL · PI MOONEY, DAVID J · 2013 to 2016
$1.5M
Programming antigen specific dendritic cells in situ for type 1 diabetes immunothF30DK088518 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SANDS, ROGER WARREN · 2010 to 2012
$126k
NIBIB NIH HHS 1R01EB015498NIBIB NIH HHS R01 EB015498NIDDK NIH HHS F30 DK088518NIDDK NIH HHS F30DK088518-03NIGMS NIH HHS T32 GM008152NIGMS NIH HHS T32-GM008152
6 · The paper itself

Abstract

Three-dimensional macroporous scaffolds have extensively been studied for cell-based tissue engineering but their use is mostly limited to mechanical support for cell adhesion and growth on the surface of macropores. Here, a templated fabrication method is described to prepare cell-friendly inverse opal-like hydrogels (IOHs) allowing both cell encapsulation within the hydrogel matrix and cell seeding on the surface of macropores. Ionically crosslinked alginate microbeads and photocrosslinkable biocompatible polymers are used as a sacrificial template and as a matrix, respectively. The alginate microbeads are easily removed by a chelating agent, with minimal toxicity for the encapsulated cells during template removal. The outer surface of macropores in IOHs can also provide a space for cell adherence. The cells encapsulated or attached in IOHs are able to remain viable and to proliferate over time. The elastic modulus and cell-adhesion properties of IOHs can be easily controlled and tuned. Finally, it is demonstrated that IOH can be used to co-culture two distinct cell populations in different spatial positions. This cell-friendly IOH system provides a 3D scaffold for organizing different cell types in a controllable microenvironment to investigate biological processes such as stem cell niches or tumor microenvironments.

Indexed as

AlginatesAnimalsBiocompatible MaterialsCell AdhesionCell Line, TumorCells, CulturedCoculture TechniquesGreen Fluorescent ProteinsHumansHuman Umbilical Vein Endothelial CellsHydrogel, Polyethylene Glycol DimethacrylateLuminescent ProteinsMesenchymal Stem CellsMiceMicroscopy, FluorescenceMicrospheresAlginatesBiocompatible MaterialsGreen Fluorescent ProteinsHydrogel, Polyethylene Glycol DimethacrylateLuminescent ProteinsPolymersRed Fluorescent Proteinalginateco-culture systemgelatinhydrogelsinverse opal structure

Identifiers

PMID25113941
PMCPMC4318565

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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.