Evidence map›Paper›PMID 32244375›Full record

ArticleMolecules (Basel, Switzerland)2020

Pre-Clinical Investigation of Keratose as an Excipient of Drug Coated Balloons.

Emily Goel, Megan Erwin, Claire V Cawthon, Carson Schaff, Nathaniel Fedor, Trevor Rayl, Onree Wilson, Uwe Christians, Thomas C Register, Randolph L Geary and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  6. The Development of anFrontiers in medical technology · 2021
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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

12 authors at 4 institutions in 1 country.

Emily GoelDepartment of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.
Megan ErwinDepartment of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.ORCID 0000-0002-7014-0856
Claire V CawthonDepartment of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.ORCID 0000-0002-9120-5479
Carson SchaffDepartment of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.
Nathaniel FedorDepartment of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.
Trevor RaylDepartment of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.
Onree WilsonDepartment of Mechanical Engineering, University of South Alabama, Mobile, AL 36688, USA.
Uwe ChristiansiC42 Clinical Research and Development, Department of Anesthesiology, University of Colorado; Aurora, CO 80045, USA.
Thomas C RegisterDepartment of Vascular Surgery, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Randolph L GearyDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Justin SaulDepartment of Chemical, Paper and Biomedical Engineering, Miami University, Oxford, OH 45056, USA.
Saami K YazdaniDepartment of Engineering, Wake Forest University, Winston-Salem, NC 27101, USA.ORCID 0000-0002-9719-6382
University of South Alabama · USWake Forest University · USMiami University · USThe Medical Center of Aurora · US

Funding

A Novel Drug Delivery System to Treat Peripheral Arterial DiseaseR15HL127596 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI YAZDANI, SAAMI K · 2016 to 2016
$413k
American Heart Association 15SDG25880000American Heart Association 16PRE27350003NHLBI NIH HHS R15 HL127596NIH HHS 1R15HL127596
6 · The paper itself

Abstract

backgroundDrug-coated balloons (DCBs), which deliver anti-proliferative drugs with the aid of excipients, have emerged as a new endovascular therapy for the treatment of peripheral arterial disease. In this study, we evaluated the use of keratose (KOS) as a novel DCB-coating excipient to deliver and retain paclitaxel.

methodsA custom coating method was developed to deposit KOS and paclitaxel on uncoated angioplasty balloons. The retention of the KOS-paclitaxel coating, in comparison to a commercially available DCB, was evaluated using a novel vascular-motion simulating

resultsThe KOS coating exhibited greater retention of the paclitaxel at 3 days under pulsatile conditions with vascular motion as compared to the commercially available DCB (14.89 ± 4.12 ng/mg vs. 0.60 ± 0.26 ng/mg,

conclusionsThe ability to enhance drug delivery and retention in targeted arterial segments can ultimately improve clinical peripheral endovascular outcomes.

Indexed as

Coated Materials, BiocompatibleDrug Delivery SystemsKeratosisAngioplasty, BalloonAnimalsAntineoplastic AgentsCardiovascular AgentsDrug CarriersDrug Evaluation, PreclinicalImmunohistochemistryPaclitaxelPeripheral Arterial DiseaseAntineoplastic AgentsCardiovascular AgentsCoated Materials, BiocompatibleDrug CarriersPaclitaxeldrug-coated balloondrug deliveryendovascularKeratosepaclitaxelperipheral arterial diseasepre-clinical

Identifiers

PMID32244375
PMCPMC7180741
OpenAlexW3015014915

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.