Evidence map›Paper›PMID 30821930›Full record

ArticleJournal of biomedical materials research. Part B, Applied biomaterials2019

Development of surface functionalization strategies for 3D-printed polystyrene constructs.

Max J Lerman, Shin Muramoto, Navein Arumugasaamy, Michael Van Order, Josephine Lembong, Anushka G Gerald, Greg Gillen, John P Fisher

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part B, Applied biomaterials, 2019. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

8 authors.

Max J LermanDepartment of Materials Science and Engineering, University of Maryland, College Park, Maryland.ORCID 0000-0001-7153-9730
Shin MuramotoSurface and Trace Chemical Analysis Group, Materials Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland.
Navein ArumugasaamyCenter for Engineering Complex Tissues, University of Maryland, College Park, Maryland.
Michael Van OrderDepartment of Materials Science and Engineering, University of Maryland, College Park, Maryland.
Josephine LembongCenter for Engineering Complex Tissues, University of Maryland, College Park, Maryland.
Anushka G GeraldCenter for Engineering Complex Tissues, University of Maryland, College Park, Maryland.
Greg GillenSurface and Trace Chemical Analysis Group, Materials Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland.
John P FisherCenter for Engineering Complex Tissues, University of Maryland, College Park, Maryland.

Funding

Training and Dissemination CoreP41EB023833 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI FISHER, JOHN P, MIKOS, ANTONIOS G. · 2017 to 2021
$6.2M
Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI HOFFMAN, ERIC P. · 2016 to 2020
$5.9M
NIBIB NIH HHS P41 EB023833NICHD NIH HHS U54 HD090257NIH HHS 1U54HD090257
6 · The paper itself

Abstract

There is a growing interest in 3D printing to fabricate culture substrates; however, the surface properties of the scaffold remain pertinent to elicit targeted and expected cell responses. Traditional 2D polystyrene (PS) culture systems typically require surface functionalization (oxidation) to facilitate and encourage cell adhesion. Determining the surface properties which enhance protein adhesion from media and cellular extracellular matrix (ECM) production remains the first step to translating 2D PS systems to a 3D culture surface. Here we show that the presence of carbonyl groups to PS surfaces correlated well with successful adhesion of ECM proteins and sustaining ECM production of deposited human mesenchymal stem cells, if the surface has a water contact angle between 50° and 55°. Translation of these findings to custom-fabricated 3D PS scaffolds reveals carbonyl groups continued to enhance spreading and growth in 3D culture. Cumulatively, these data present a method for 3D printing PS and the design considerations required for understanding cell-material interactions. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B:2566-2578, 2019.

Indexed as

Printing, Three-DimensionalAnimalsCattleHumansMesenchymal Stem CellsPolystyrenesSurface PropertiesTissue ScaffoldsPolystyrenes3D printingplasma treatmentpolystyreneprotein adhesionsurface chemical modification

Identifiers

PMID30821930
PMCPMC10320806

What OpenQuestion holds

Textmetadata
LicenceTDM
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.