Evidence map›Paper›PMID 35163411›Full record

ArticleInternational journal of molecular sciences2022

An Innovative Customized Biomimetic Hydrogel for Drug Screening Application Potential: Biocompatibility and Cell Invasion Ability.

Keng-Liang Ou, Chiung-Fang Huang, Wen-Chien Lan, Bai-Hung Huang, Hsu-An Pan, Yung-Kang Shen, Takashi Saito, Hsin-Yu Tsai, Yung-Chieh Cho, Kuo-Sheng Hung and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 51% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Printable Hydrogels Based on Alginate and Halloysite Nanotubes.International journal of molecular sciences · 2022
    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

11 authors at 6 institutions in 2 countries.

Keng-Liang OuDepartment of Dentistry, Taipei Medical University-Shuang Ho Hospital, New Taipei City 235, Taiwan.ORCID 0000-0003-1786-6305
Chiung-Fang HuangSchool of Dental Technology, College of Oral Medicine, Taipei Medical University, Taipei 110, Taiwan.
Wen-Chien LanDepartment of Oral Hygiene Care, Ching Kuo Institute of Management and Health, Keelung 203, Taiwan.
Bai-Hung HuangBiomedical Technology R&D Center, China Medical University, Taichung 404, Taiwan.
Hsu-An PanBiomedical Technology R&D Center, China Medical University, Taichung 404, Taiwan.
Yung-Kang ShenSchool of Dental Technology, College of Oral Medicine, Taipei Medical University, Taipei 110, Taiwan.
Takashi SaitoDivision of Medicine for Function and Morphology of Sensor Organs, Department of Dentistry and Oral Surgery, Osaka Medical College, Osaka 569-8686, Japan.ORCID 0000-0001-8816-7187
Hsin-Yu TsaiDivision of Medicine for Function and Morphology of Sensor Organs, Department of Dentistry and Oral Surgery, Osaka Medical College, Osaka 569-8686, Japan.
Yung-Chieh ChoBiomedical Technology R&D Center, China Medical University, Taichung 404, Taiwan.
Kuo-Sheng HungGraduate Institute of Injury Prevention and Control, College of Public Health, Taipei Medical University, Taipei 110, Taiwan.
Hsin-Hua ChouSchool of Oral Hygiene, College of Oral Medicine, Taipei Medical University, Taipei 110, Taiwan.
China Medical University · TWOsaka Medical and Pharmaceutical University · JPWan Fang Hospital · TWChing Kuo Institute of Management and Health · TWTaipei Medical University · TWTaipei Medical University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability of Pluronic F127 (PF127) conjugated with tetrapeptide Gly-Arg-Gly-Asp (GRGD) as a sequence of Arg-Gly-Asp (RGD) peptide to form the investigated potential hydrogel (hereafter referred to as 3DG bioformer (3BE)) to produce spheroid, biocompatibility, and cell invasion ability, was assessed in this study. The fibroblast cell line (NIH 3T3), osteoblast cell line (MG-63), and human breast cancer cell line (MCF-7) were cultured in the 3BE hydrogel and commercial product (Matrigel) for comparison. The morphology of spheroid formation was evaluated via optical microscopy. The cell viability was observed through cell counting Kit-8 assay, and cell invasion was investigated via Boyden chamber assay. Analytical results indicated that 3BE exhibited lower spheroid formation than Matrigel. However, the 3BE appeared biocompatible to NIH 3T3, MG-63, and MCF-7 cells. Moreover, cell invasion ability and cell survival rate after invasion through the 3BE was displayed to be comparable to Matrigel. Thus, these findings demonstrate that the 3BE hydrogel has a great potential as an alternative to a three-dimensional cell culture for drug screening applications.

Indexed as

AnimalsBiocompatible MaterialsBiomimetic MaterialsDrug Evaluation, PreclinicalHumansHydrogelsMCF-7 CellsMiceNIH 3T3 CellsOligopeptidesPoloxamerBiocompatible Materialsglycyl-arginyl-glycyl-aspartic acidHydrogelsOligopeptidesPoloxamerdrug screeninghydrogelPluronic F127RGD peptidespheroid

Identifiers

PMID35163411
PMCPMC8835991
OpenAlexW4210651613

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.