Evidence map›Paper›PMID 37899763›Full record

ArticleAsian biomedicine : research, reviews and news2023

Alginate-gelatin hydrogel supplemented with platelet concentrates can be used as bioinks for scaffold printing.

Tuyet Thi Vi Le, Nghia Thi Hieu Phan, Ha Le Bao Tran

Open access · hybridAbstract read
In one paragraph

Article in Asian biomedicine : research, reviews and news, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

3 authors at 2 institutions in 1 country.

Tuyet Thi Vi LeDepartment of Physiology and Animal Biotechnology, Biology and Biotechnology Faculty, University of Science, Ho Chi Minh City 700000, Vietnam.
Nghia Thi Hieu PhanDepartment of Physiology and Animal Biotechnology, Biology and Biotechnology Faculty, University of Science, Ho Chi Minh City 700000, Vietnam.
Ha Le Bao TranDepartment of Physiology and Animal Biotechnology, Biology and Biotechnology Faculty, University of Science, Ho Chi Minh City 700000, Vietnam.
Vietnam National University Ho Chi Minh City · VNHo Chi Minh City University of Science · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Owing to the growing global demand for organ replacement and tissue regeneration, three-dimensional (3D) printing is widely recognized as an essential technology in tissue engineering. Biomaterials become a potential source of raw materials for printing ink by containing factors that promote tissue regeneration. Platelet concentrates are autologous biological products that are capable of doing that. Objectives: This study was carried out to create bioinks capable of providing biological signals by combining gelatin-alginate with platelet concentrates. Methods: This study combined platelet concentrates, including platelet-rich plasma (PRP) and platelet-rich fibrin (PRF), with gelatin and alginate to create bioinks. Bioink properties, including gelatinization and pH, were assessed before printing. After that, the scaffolds were done, and the growth factor (GF) release and cytotoxicity from these scaffolds were performed. Results: Results showed that all the three bioinks, including alginate-gelatin (AG), alginate-gelatin-PRP (AGP), and alginate-gelatin-PRF (AGF) were gelatinized right at the end of bioink fabrication and had a pH around 7. The scaffolds from bioinks supplemented with platelet concentrates secreted GFs that remained for 12 d, and the extracts from them were not cytotoxic for the L929 cell line. Conclusion: In summary, bioinks were made by combining AG with platelet concentrates and had properties suitable for creating scaffolds with cell-oriented grafts in the development of artificial tissues and organs.

Indexed as

bioinksbiosignalsgrowth factorshydrogelsprintingscaffoldstissue regeneration

Identifiers

PMID37899763
PMCPMC10602633
OpenAlexW4388035333

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.