Evidence map›Paper›PMID 34881524›Full record

ArticleAdvanced healthcare materials2022

Polysalicylic Acid Polymer Microparticle Decoys Therapeutically Treat Acute Respiratory Distress Syndrome.

Emma R Brannon, William J Kelley, Michael W Newstead, Alison L Banka, Kathryn E Uhrich, Colleen E O'Connor, Theodore J Standiford, Omolola Eniola-Adefeso

Open access · bronzeAbstract read
In one paragraph

Article in Advanced healthcare materials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 18 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

8 authors at 3 institutions in 1 country.

Emma R BrannonDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
William J KelleyDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Michael W NewsteadDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI, 48109, USA.
Alison L BankaDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Kathryn E UhrichDepartment of Chemistry, University of California Riverside, Riverside, CA, 92521, USA.
Colleen E O'ConnorDepartment of Bioengineering, University of Washington, Seattle, WA, 98195, USA.
Theodore J StandifordDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI, 48109, USA.
Omolola Eniola-AdefesoDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID 0000-0002-8728-6608
University of Michigan · USUniversity of California, Riverside · USUniversity of Washington · US

Funding

Cellular Biotechnology Training Program (CBTP)T32GM008353 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHWENDEMAN, ANNA · 1991 to 2021
$9.3M
Cellular Biotechnology Training Program (CBTP) - Years 31-35T32GM145304 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Guizhi Zhu · 2022 to 2026
$2.6M
Development of PolyAspirin Particles for Therapeutic Intervention in ALI/ARDS via the Passive Restraint of Neutrophil FunctionR01HL145709 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SINGER, BENJAMIN HERSCHEL · 2020 to 2023
$1.6M
NHLBI NIH HHS R01 HL145709NIGMS NIH HHS T32 GM008353NIGMS NIH HHS T32 GM145304
6 · The paper itself

Abstract

Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) remain problematic due to high mortality rates and lack of effective treatments. Neutrophilic injury contributes to mortality in ALI/ARDS. Here, technology for rapid ARDS intervention is developed and evaluated, where intravenous salicylic acid-based polymer microparticles, i.e., Poly-Aspirin (Poly-A), interfere with neutrophils in blood, reducing lung neutrophil infiltration and injury in vivo in mouse models of ALI/ARDS. Importantly, Poly-A particles reduce multiple inflammatory cytokines in the airway and bacterial load in the bloodstream in a live bacteria lung infection model of ARDS, drastically improving survival. It is observed that phagocytosis of the Poly-A microparticles, with salicylic acid in the polymer backbone, alters the neutrophil surface expression of adhesion molecules, potentially contributing to their added therapeutic benefits. Given the proven safety profile of the microparticle degradation products-salicylic acid and adipic acid-it is anticipated that the Poly-A particles represent a therapeutic strategy in ARDS with a rare opportunity for rapid clinical translation.

Indexed as

Acute Lung InjuryRespiratory Distress SyndromeAnimalsMiceNeutrophil InfiltrationPolymersSalicylic AcidPolymersSalicylic Acidinflammationlung injurymicroparticlesneutrophilsphagocytosis

Identifiers

PMID34881524
PMCPMC8986552
OpenAlexW4200326675

What OpenQuestion holds

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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.