Evidence map›Paper›PMID 33919677›Full record

ArticleInternational journal of molecular sciences2021

Large-Pore Platelet-Rich Fibrin with a Mg Ring to Allow MC3T3-E1 Preosteoblast Migration and to Improve Osteogenic Ability for Bone Defect Repair.

Pei-Chun Wong, Chen-Yun Wang, Jason Shian-Ching Jang, Chian-Her Lee, Jia-Lin Wu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

3 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Platelet rich fibrin is not a barrier membrane! Or is it?World journal of clinical cases · 2023
    Review
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

5 authors at 3 institutions in 1 country.

Pei-Chun WongDepartment of Orthopedics, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.ORCID 0000-0001-8357-5616
Chen-Yun WangSchool of Biomedical Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei 110, Taiwan.
Jason Shian-Ching JangInstitute of Materials Science and Engineering, National Central University, Taoyuan 33043, Taiwan.ORCID 0000-0003-1507-3248
Chian-Her LeeDepartment of Orthopedics, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
Jia-Lin WuDepartment of Orthopedics, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.ORCID 0000-0002-2843-405X
Taipei Medical University Hospital · TWNational Central University · TWTaipei Medical University · TW

Funding

Ministry of Science and Technology of Taiwan MOST109-2314-B-038-149Taipei Medical University Hospital 109TMUH-NE-06
6 · The paper itself

Abstract

Platelet-rich fibrin (PRF) is a natural fibrin meshwork material with multiple functions that are suitable for tissue engineering applications. PRF provides a suitable scaffold for critical-size bone defect treatment due to its platelet cytokines and rich growth factors. However, the structure of PRF not only promotes cell attachment but also, due to its density, provides a pool for cell migration into the PRF to facilitate regeneration. In our study, we used repeated freeze drying to enlarge the pores of PRF to engineer large-pore PRF (LPPRF), a type of PRF that has expanded pores for cell migration. Moreover, a biodegradable Mg ring was used to provide stability to bone defects and the release of Mg ions during degradation may enhance osteoconduction and osteoinduction. Our results revealed that cell migration was more extensive when LPPRF was used rather than when PRF was used and that LPPRF retained the growth factors present in PRF. Moreover, the Mg ions released from the Mg ring during degradation significantly enhanced the calcium deposition of MC3T3-E1 preosteoblasts. In the present study, a bone substitute comprising LPPRF combined with a Mg ring was demonstrated to have much potential for critical-size bone defect repair.

Indexed as

Wound HealingAnimalsBone and BonesCalciumCell DifferentiationCell LineCell MovementCell ProliferationCells, CulturedCell ShapeCell SurvivalIntercellular Signaling Peptides and ProteinsMagnesiumMiceOsteoblastsOsteogenesisCalciumIntercellular Signaling Peptides and ProteinsMagnesiumTitaniumbone defectcalcium depositiondegradationlarge-pore platelet-rich fibrinMg ringmigrationrepeated freeze drying method

Identifiers

PMID33919677
PMCPMC8070656
OpenAlexW3156001098

What OpenQuestion 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 OpenQuestion graph.