Evidence map›Paper›PMID 28648052›Full record

ArticleACS applied materials & interfaces2017

Anticancer Therapeutic Alginate-Based Tissue Sealants for Lung Repair.

Spencer L Fenn, Patrick N Charron, Rachael A Floreani

Open access · greenAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 38 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

3 authors at 1 institution in 1 country.

Spencer L FennDepartment of Biomedical Engineering, Tufts University , Medford, Massachusetts 02155, United States.ORCID 0000-0001-9379-1582
Patrick N CharronDepartment of Mechanical Engineering, College of Engineering and Mathematical Sciences, University of Vermont , Burlington, Vermont 05405, United States.
Rachael A FloreaniBioengineering Program, College of Engineering and Mathematical Sciences, and Larner College of Medicine, University of Vermont , Burlington, Vermont 05405, United States.
University of Vermont · US

Funding

Multidisciplinary Training in Lung BiologyT32HL076122 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI IRVIN, CHARLES G, POYNTER, MATTHEW E · 2004 to 2023
$6.1M
Development of a Polysaccharide-Based Patch for Use as a Therapeutic Lung SealantR01EB020964 · NIBIB · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI FLOREANI, RACHAEL · 2016 to 2019
$1.5M
NHLBI NIH HHS T32 HL076122NIBIB NIH HHS R01 EB020964
6 · The paper itself

Abstract

Injury to the connective tissue that lines the lung, the pleura, or the lung itself can occur from many causes including trauma or surgery, as well as lung diseases or cancers. To address current limitations for patching lung injuries, to stop air or fluid leaks, an adherent hydrogel sealant patch system was developed, based on methacrylated alginate (AMA) and AMA dialdehyde (AMA-DA) blends, which is capable of sealing damaged tissues and sustaining physiological pressures. Methacrylation of alginate hydroxyl groups rendered the polysaccharide capable of photo-cross-linking when mixed with an eosin Y-based photoinitiator system and exposed to visible green light. Oxidation of alginate yields functional aldehyde groups capable of imine bond formation with proteins found in many tissues. The alginate-based patch system was rigorously tested on a custom burst pressure testing device. Blending of nonoxidized material with oxidized (aldehyde modified) alginates yielded patches with improved burst pressure performance and decreased delamination as compared with pure AMA. Human mesothelial cell (MeT-5A) viability and cytotoxicity were retained when cultured with the hydrogel patches. The release and bioactivity of doxorubicin-encapsulated submicrospheres enabled the fabrication of drug-eluting adhesive patches and were effective in decreasing human lung cancer cell (A549) viability.

Indexed as

AlginatesAlginic AcidAntineoplastic AgentsGlucuronic AcidHexuronic AcidsHumansHydrogelsAlginatesAlginic AcidAntineoplastic AgentsGlucuronic AcidHexuronic AcidsHydrogelsaldehydealginateburst pressuredrug deliverylungtissue sealantvisible-light cross-linking

Identifiers

PMID28648052
PMCPMC5546308
OpenAlexW2716286825

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.