Evidence map›Paper›PMID 30120625›Full record

ArticleJournal of materials science. Materials in medicine2018

Pluronic F127 blended polycaprolactone scaffolds via e-jetting for esophageal tissue engineering.

Bin Wu, Nobuyoshi Takeshita, Yang Wu, Sanjairaj Vijayavenkataraman, Khek Yu Ho, Wen Feng Lu, Jerry Ying Hsi Fuh

Abstract read
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In one paragraph

Article in Journal of materials science. Materials in medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 16% of its field
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

9 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Nanoformulation of CCL21 greatly increases its effectiveness as an immunotherapy for neuroblastoma.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
  7. Article
  8. Article
  9. Rapid and efficientInternational journal of bioprinting · 2019
    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

7 authors at 2 institutions in 2 countries.

Bin WuDepartment of Mechanical Engineering, National University of Singapore, Singapore, 117576, Singapore.
Nobuyoshi TakeshitaYong Loo Lin School of Medicine, National University of Singapore, Singapore, 119228, Singapore.
Yang WuEngineering Science and Mechanics Department, Penn State University, University Park, PA, 16802, USA.
Sanjairaj VijayavenkataramanDepartment of Mechanical Engineering, National University of Singapore, Singapore, 117576, Singapore.
Khek Yu HoYong Loo Lin School of Medicine, National University of Singapore, Singapore, 119228, Singapore.
Wen Feng LuDepartment of Mechanical Engineering, National University of Singapore, Singapore, 117576, Singapore.
Jerry Ying Hsi FuhDepartment of Mechanical Engineering, National University of Singapore, Singapore, 117576, Singapore. jerry.fuh@nus.edu.sg.
National University of Singapore · SGPennsylvania State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several attempts have been made to fabricate esophageal tissue engineering scaffolds. However, most of these scaffolds possess randomly oriented fibres and uncontrollable pore sizes. In order to mimic the native esophageal tissue structure, electro-hydrodynamic jetting (e-jetting) was used in this study to fabricate scaffolds with aligned fibres and controlled pore size. A hydrophilic additive, Pluronic F127 (F127), was blended with polycaprolactone (PCL) to improve the wettability of the scaffolds and hence the cell adhesion. PCL/F127 composite scaffolds with different weight ratios (0-12%) were fabricated. The wettability, phase composition, and the mechanical properties of the fabricated scaffolds were investigated. The results show that the e-jetted scaffolds have controllable fibres orientated in two perpendicular directions, which are similar to the human esophagus structure and suitable pore size for cell infiltration. In addition, the scaffolds with 8% F127 exhibited better wettability (contact angle of 14°) and an ultimate tensile strength (1.2 MPa) that mimics the native esophageal tissue. Furthermore, primary human esophageal fibroblasts were seeded on the e-jetted scaffolds. PCL/F127 scaffolds showed enhanced cell proliferation and expression of the vascular endothelial growth factor (VEGF) compared to pristine PCL scaffolds (1.5- and 25.8- fold increase, respectively; P < 0.001). An in vitro wound model made using the PCL/F127 scaffolds showed better cell migration than the PCL scaffolds. In summary, the PCL/F127 e-jetted scaffolds offer a promising strategy for the esophagus tissue repair.

Indexed as

EsophagusTissue ScaffoldsCell AdhesionCell ProliferationCell SurvivalFibroblastsHumansHydrophobic and Hydrophilic InteractionsImaging, Three-DimensionalMaterials TestingMicroscopy, ConfocalPoloxamerPolyestersPorosityStress, MechanicalTensile StrengthPoloxamerpolycaprolactonePolyestersVascular Endothelial Growth Factor A

Identifiers

PMID30120625
OpenAlexW2886196570

What OpenQuestion holds

Textmetadata
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.