Evidence map›Paper›PMID 35442705›Full record

ArticleScience translational medicine2022

Reactive oxygen species-degradable polythioketal urethane foam dressings to promote porcine skin wound repair.

Prarthana Patil, Katherine A Russo, Joshua T McCune, Alonda C Pollins, Matthew A Cottam, Bryan R Dollinger, Carlisle R DeJulius, Mukesh K Gupta, Richard D'Arcy, Juan M Colazo and 10 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
11.4field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 118 citations in OpenAlex.

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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

20 authors at 3 institutions in 1 country.

Prarthana PatilDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0002-3708-301X
Katherine A RussoDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Joshua T McCuneDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0003-4984-176X
Alonda C PollinsDepartment of Plastic Surgery, Vanderbilt University Medical Center, Nashville, TN 37212, USA.ORCID 0000-0002-8331-7665
Matthew A CottamDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.ORCID 0000-0003-0619-1605
Bryan R DollingerDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Carlisle R DeJuliusDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Mukesh K GuptaDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0002-9571-3454
Richard D'ArcyDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0002-8567-368X
Juan M ColazoDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0002-3591-4246
Fang YuDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0002-9022-2410
Mariah G BezoldDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0002-2616-4826
John R MartinDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0003-1681-3818
Nancy L CardwellDepartment of Plastic Surgery, Vanderbilt University Medical Center, Nashville, TN 37212, USA.ORCID 0000-0002-5221-898X
Jeffrey M DavidsonDepartment of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.ORCID 0000-0002-8782-3565
Callie M ThompsonVanderbilt Burn Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0002-1529-5687
Adrian BarbulDepartment of Surgery, Vanderbilt University Medical Center, Nashville, TN 37212, USA.ORCID 0000-0002-6283-6255
Alyssa H HastyDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Scott A GuelcherDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0002-9871-8058
Craig L DuvallDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0003-3979-0620
Vanderbilt University · USVanderbilt University Medical Center · USUnited States Department of Veterans Affairs · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ben Ho Park · 1995 to 2026
$172.8M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Substrate Mediated siRNA Delivery from Scaffolds to Promote Wound RepairR01EB019409 · NIBIB · VANDERBILT UNIVERSITY · PI Craig Lewis Duvall · 2014 to 2026
$4.0M
Integrated Training in Engineering and DiabetesT32DK101003 · NIDDK · VANDERBILT UNIVERSITY · PI Jamey D. Young · 2014 to 2026
$3.9M
Hybrid Synthetic and Biologic Shear Thinning Hydrogels for Diabetic Wound HealingR01EB028690 · NIBIB · VANDERBILT UNIVERSITY · PI DUVALL, CRAIG LEWIS, GUPTA, MUKESH KUMAR · 2019 to 2023
$2.0M
BLRD Merit Review Research Career Scientist (RCS) Award (IK6)IK6BX005649 · VA · VETERANS HEALTH ADMINISTRATION · PI HASTY, ALYSSA H · 2021 to 2023
–
BLRD VA IK6 BX005649NCI NIH HHS P30 CA068485NIBIB NIH HHS R01 EB019409NIBIB NIH HHS R01 EB028690NIDDK NIH HHS T32 DK101003NIDDK NIH HHS U24 DK059637
6 · The paper itself

Abstract

Porous, resorbable biomaterials can serve as temporary scaffolds that support cell infiltration, tissue formation, and remodeling of nonhealing skin wounds. Synthetic biomaterials are less expensive to manufacture than biologic dressings and can achieve a broader range of physiochemical properties, but opportunities remain to tailor these materials for ideal host immune and regenerative responses. Polyesters are a well-established class of synthetic biomaterials; however, acidic degradation products released by their hydrolysis can cause poorly controlled autocatalytic degradation. Here, we systemically explored reactive oxygen species (ROS)-degradable polythioketal (PTK) urethane (UR) foams with varied hydrophilicity for skin wound healing. The most hydrophilic PTK-UR variant, with seven ethylene glycol (EG7) repeats flanking each side of a thioketal bond, exhibited the highest ROS reactivity and promoted optimal tissue infiltration, extracellular matrix (ECM) deposition, and reepithelialization in porcine skin wounds. EG7 induced lower foreign body response, greater recruitment of regenerative immune cell populations, and resolution of type 1 inflammation compared to more hydrophobic PTK-UR scaffolds. Porcine wounds treated with EG7 PTK-UR foams had greater ECM production, vascularization, and resolution of proinflammatory immune cells compared to polyester UR foam-based NovoSorb Biodegradable Temporizing Matrix (BTM)-treated wounds and greater early vascular perfusion and similar wound resurfacing relative to clinical gold standard Integra Bilayer Wound Matrix (BWM). In a porcine ischemic flap excisional wound model, EG7 PTK-UR treatment led to higher wound healing scores driven by lower inflammation and higher reepithelialization compared to NovoSorb BTM. PTK-UR foams warrant further investigation as synthetic biomaterials for wound healing applications.

Indexed as

Biocompatible MaterialsWound HealingAnimalsBandagesInflammationPolyestersReactive Oxygen SpeciesSkinSwineBiocompatible MaterialsPolyestersReactive Oxygen Species

Identifiers

PMID35442705
PMCPMC10165619
OpenAlexW4224240832

What OpenQuestion holds

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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.