Evidence map›Paper›PMID 29698603›Full record

ArticleBiomacromolecules2018

Zwitterionic PEG-PC Hydrogels Modulate the Foreign Body Response in a Modulus-Dependent Manner.

Lauren E Jansen, Luke D Amer, Esther Y-T Chen, Thuy V Nguyen, Leila S Saleh, Todd Emrick, Wendy F Liu, Stephanie J Bryant, Shelly R Peyton

Open access · greenAbstract read
In one paragraph

Article in Biomacromolecules, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 111 citations in OpenAlex.

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  13. Biomaterial-Based Therapeutic Delivery of Immune Cells.Advanced healthcare materials · 2025
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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

9 authors at 3 institutions in 1 country.

Lauren E Jansen
Luke D AmerDepartment of Chemical and Biological Engineering , University of Colorado Boulder , Boulder , Colorado 80309 , United States.
Esther Y-T ChenDepartment of Biomedical Engineering , University of California, Irvine , Irvine , California 92697 , United States.
Thuy V Nguyen
Leila S SalehDepartment of Chemical and Biological Engineering , University of Colorado Boulder , Boulder , Colorado 80309 , United States.
Wendy F LiuDepartment of Biomedical Engineering , University of California, Irvine , Irvine , California 92697 , United States.
Stephanie J BryantDepartment of Chemical and Biological Engineering , University of Colorado Boulder , Boulder , Colorado 80309 , United States.
University of Massachusetts Amherst · USUniversity of Colorado Boulder · USUniversity of California, Irvine · US

Funding

Tissue-specific stem cells and breast cancer tissue tropism in bioengineered microenvironmentsDP2CA186573 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI PEYTON, SHELLY R. · 2013 to 2015
$2.6M
Engineering Biomaterials to Exert Molecular Control of Immune Cell FunctionDP2DE023319 · NIDCR · UNIVERSITY OF CALIFORNIA-IRVINE · PI LIU, WENDY · 2012 to 2012
$2.3M
Acquisition of an Orbitrap MSS10OD010645 · OD · UNIVERSITY OF MASSACHUSETTS AMHERST · PI EYLES, STEPHEN J. · 2013 to 2013
$600k
The Interplay between Macrophages and Differentiating MSCs in Cell-Laden HydrogelR21AR064436 · NIAMS · UNIVERSITY OF COLORADO · PI BRYANT, STEPHANIE J · 2013 to 2014
$358k
NCI NIH HHS DP2 CA186573NIAMS NIH HHS R21 AR064436NIDCR NIH HHS DP2 DE023319NIH HHS S10 OD010645
6 · The paper itself

Abstract

Reducing the foreign body response (FBR) to implanted biomaterials will enhance their performance in tissue engineering. Poly(ethylene glycol) (PEG) hydrogels are increasingly popular for this application due to their low cost, ease of use, and the ability to tune their compliance via molecular weight and cross-linking densities. PEG hydrogels can elicit chronic inflammation in vivo, but recent evidence has suggested that extremely hydrophilic, zwitterionic materials and particles can evade the immune system. To combine the advantages of PEG-based hydrogels with the hydrophilicity of zwitterions, we synthesized hydrogels with comonomers PEG and the zwitterion phosphorylcholine (PC). Recent evidence suggests that stiff hydrogels elicit increased immune cell adhesion to hydrogels, which we attempted to reduce by increasing hydrogel hydrophilicity. Surprisingly, hydrogels with the highest amount of zwitterionic comonomer elicited the highest FBR. Lowering the hydrogel modulus (165 to 3 kPa), or PC content (20 to 0 wt %), mitigated this effect. A high density of macrophages was found at the surface of implants associated with a high FBR, and mass spectrometry analysis of the proteins adsorbed to these gels implicated extracellular matrix, immune response, and cell adhesion protein categories as drivers of macrophage recruitment. Overall, we show that modulus regulates macrophage adhesion to zwitterionic-PEG hydrogels, and demonstrate that chemical modifications to hydrogels should be studied in parallel with their physical properties to optimize implant design.

Indexed as

AnimalsCell AdhesionCells, CulturedForeign-Body ReactionHydrogelsHydrophobic and Hydrophilic InteractionsMacrophagesMaleMiceMice, Inbred C57BLPhosphorylcholinePolyethylene GlycolsHydrogelsPhosphorylcholinePolyethylene Glycols

Identifiers

PMID29698603
PMCPMC6190668
OpenAlexW2765306627

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.