Evidence map›Paper›PMID 29242160›Full record

ArticleActa biomaterialia2018

The impact of functional groups of poly(ethylene glycol) macromers on the physical properties of photo-polymerized hydrogels and the local inflammatory response in the host.

James R Day, Anu David, Jiwon Kim, Evan A Farkash, Marilia Cascalho, Nikola Milašinović, Ariella Shikanov

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  4. 3DFrontiers in pharmacology · 2025
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  6. A review of advanced hydrogels for cartilage tissue engineering.Frontiers in bioengineering and biotechnology · 2024
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  7. Review
  8. Article
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  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Facile Cell-Friendly Hollow-Core Fiber Diffusion-Limited Photofabrication.Frontiers in bioengineering and biotechnology · 2021
    Article
  17. Article
  18. Article
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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 1 country.

James R DayUniversity of Michigan, Department of Biomedical Engineering, 1101 Beal Avenue, Ann Arbor 48109, MI, USA. Electronic address: dayjr@umich.edu.
Anu DavidUniversity of Michigan, Department of Biomedical Engineering, 1101 Beal Avenue, Ann Arbor 48109, MI, USA. Electronic address: anudavid@umich.edu.
Jiwon KimUniversity of Michigan, Department of Biomedical Engineering, 1101 Beal Avenue, Ann Arbor 48109, MI, USA. Electronic address: jiwonk@umich.edu.
Evan A FarkashUniversity of Michigan Medical School, Department of Pathology, Ann Arbor 48109, MI, USA. Electronic address: efarkash@med.umich.edu.
Marilia CascalhoUniversity of Michigan Medical School, Transplantation Biology, Medical Science Research Building I, 1150 West Medical Center Drive, A520B, Ann Arbor 48109, MI, USA. Electronic address: marilia@umich.edu.
Nikola MilašinovićDepartment of Forensics, Academy of Criminalistic and Police Studies, Cara Dušana 196, 11080 Belgrade, Serbia. Electronic address: nikola.milasinovic@kpa.edu.rs.
Ariella ShikanovUniversity of Michigan, Department of Biomedical Engineering, 1101 Beal Avenue, Ann Arbor 48109, MI, USA; University of Michigan, Department of Macromolecular Sciences and Engineering, 1101 Beal Avenue, Ann Arbor 48109, MI, USA. Electronic address: shikanov@umich.edu.
University of Michigan–Ann Arbor · USRegional West Medical Center · US

Funding

Engineering an immuno-isolating hydrogel for restoring ovarian endocrine functionR01EB022033 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHIKANOV, ARIELLA · 2016 to 2019
$1.5M
C4d-independent diagnosis of chronic antibody mediated renal allograft rejectionK23AI108951 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FARKASH, EVAN A · 2014 to 2018
$706k
NIAID NIH HHS K23 AI108951NIBIB NIH HHS R01 EB022033
6 · The paper itself

Abstract

Poly(ethylene glycol) (PEG) can be functionalized and modified with various moieties allowing for a multitude of cross-linking chemistries. Here, we investigate how vinyl sulfone, acrylate, and maleimide functional end groups affect hydrogel formation, physical properties, viability of encapsulated cells, post-polymerization modification, and inflammatory response of the host. We have shown that PEG-VS hydrogels, in the presence of a co-monomer, N-vinyl-2-pyrrolidone (NVP), form more efficiently than PEG-Ac and PEG-Mal hydrogels, resulting in superior physical properties after 6 min of ultraviolet light exposure. PEG-VS hydrogels exhibited hydrolytic stability and non-fouling characteristics, as well as the ability to be modified with biological motifs, such as RGD, after polymerization. Additionally, unmodified PEG-VS hydrogels resulted in lesser inflammatory response, cellular infiltration, and macrophage recruitment after implantation for 28 days in mice. These findings show that altering the end group chemistry of PEG macromer impacts characteristics of the photo-polymerized network. We have developed a tunable non-degradable PEG system that is conducive for cell or tissue encapsulation and evokes a minimal inflammatory response, which could be utilized for future immunoisolation applications. STATEMENT OF SIGNIFICANCE: The objective of this study was to develop a tunable non-degradable PEG system that is conducive for encapsulation and evokes a minimal inflammatory response, which could be utilized for immunoisolation applications. This study has demonstrated that reactive functional groups of the PEG macromers impact free radical mediated network formation. Here, we show PEG-VS hydrogels meet the design criteria for an immunoisolating device as PEG-VS hydrogels form efficiently via photo-polymerization, impacting bulk properties, was stable in physiological conditions, and elicited a minimal inflammatory response. Further, NVP can be added to the precursor solution to expedite the cross-linking process without impacting cellular response upon encapsulation. These findings present an additional approach/chemistry to encapsulate cells or tissue for immunoisolation applications.

Indexed as

LightPolymerizationAnimalsCell SurvivalCross-Linking ReagentsElastic ModulusEmbryo, MammalianFemaleFibroblastsHydrogelsHydrolysisImplants, ExperimentalInflammationMiceOligopeptidesPolyethylene Glycolsarginyl-glycyl-aspartic acidCross-Linking Reagentsdivinyl sulfoneHydrogelsN-vinyl-2-pyrrolidinoneOligopeptidesPolyethylene GlycolsProtective AgentsPyrrolidinonesSulfonesFunctional groupsInflammatory responsePhoto-polymerizationPoly(ethylene glycol)RGD modification

Identifiers

PMID29242160
PMCPMC5794611
OpenAlexW2772032673

What OpenQuestion holds

Textmetadata
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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.