Evidence map›Paper›PMID 36132391›Full record

ArticleNanoscale advances2020

New volumetric CNT-doped gelatin-cellulose scaffolds for skeletal muscle tissue engineering.

Ferran Velasco-Mallorquí, Juan M Fernández-Costa, Luisa Neves, Javier Ramón-Azcón

Abstract read
In one paragraph

Article in Nanoscale advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Tissue Engineered 3D Constructs for Volumetric Muscle Loss.Annals of biomedical engineering · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Highlights on Advancing Frontiers in Tissue Engineering.Tissue engineering. Part B, Reviews · 2022
    Review
  15. Article
  16. Review
  17. Review
  18. Current Strategies for the Regeneration of Skeletal Muscle Tissue.International journal of molecular sciences · 2021
    Review
  19. BioengineeredJournal of tissue engineering
    Review
  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.

Ferran Velasco-MallorquíInstitute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST) Baldiri I Reixac 10-12 Barcelona Spain jramon@ibecbarcelona.eu.
Juan M Fernández-CostaInstitute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST) Baldiri I Reixac 10-12 Barcelona Spain jramon@ibecbarcelona.eu.ORCID https://orcid.org/0000-0002-1854-6082
Luisa NevesMultiwave Imaging, Hotel Technoptic 2 Rue Marc Donadille 13013 Marseille France.
Javier Ramón-AzcónInstitute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST) Baldiri I Reixac 10-12 Barcelona Spain jramon@ibecbarcelona.eu.ORCID https://orcid.org/0000-0002-3636-8013

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, the fabrication of scaffolds for engineered skeletal muscle tissues is unable to reach the millimeter size. The main drawbacks are the poor nutrient diffusion, lack of an internal structure to align the precursor cells, and poor mechanical and electric properties. Herein, we present a combination of gelatin-carboxymethyl cellulose materials polymerised by a cryogelation process that allowed us to reach scaffold fabrication up to millimeter size and solve the main problems related to the large size muscle tissue constructs. (1) By incorporating carbon nanotubes (CNT), we can improve the electrical properties of the scaffold, thereby enhancing tissue maturation when applying an electric pulse stimulus (EPS). (2) We have fabricated an anisotropic internal three-dimensional microarchitecture with good pore distribution and highly aligned morphology to enhance the cell alignment, cell fusion and myotube formation. With this set up, we were able to generate a fully functional skeletal muscle tissue using a combination of EPS and our doped-biocomposite scaffold and obtain a mature tissue on the millimeter scale. We also characterized the pore distribution, swelling, stiffness and conductivity of the scaffold. Moreover, we proved that the cells were viable and could fuse in three-dimensional (3D) functional myotubes throughout the scaffold. In conclusion, we fabricated a biocompatible and customizable scaffold for 3D cell culture suitable for a wide range of applications such as organ-on-a-chip, drug screening, transplantation and disease modelling.

Identifiers

PMID36132391
PMCPMC9418820

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.