Evidence map›Paper›PMID 38488736›Full record

ArticleACS applied materials & interfaces2024

Effects of Drag-Reducing Polymers on Hemodynamics and Whole Blood-Endothelial Interactions in 3D-Printed Vascular Topologies.

Louis S Paone, Matthew Szkolnicki, Brandon J DeOre, Kiet A Tran, Noah Goldman, Allison M Andrews, Servio H Ramirez, Peter A Galie

Open access · hybridAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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 2 institutions in 1 country.

Louis S PaoneDepartment of Biomedical Engineering, Rowan University, Glassboro, New Jersey 08028, United States.ORCID 0000-0002-4098-2569
Matthew SzkolnickiDepartment of Biomedical Engineering, Rowan University, Glassboro, New Jersey 08028, United States.
Brandon J DeOreDepartment of Biomedical Engineering, Rowan University, Glassboro, New Jersey 08028, United States.
Kiet A TranDepartment of Biomedical Engineering, Rowan University, Glassboro, New Jersey 08028, United States.
Noah GoldmanDepartment of Biomedical Engineering, Rowan University, Glassboro, New Jersey 08028, United States.
Allison M AndrewsDepartment of Pathology, Immunology, & Laboratory Medicine, College of Medicine, University of Florida, Gainesville, Florida 32611, United States.
Servio H RamirezDepartment of Pathology, Immunology, & Laboratory Medicine, College of Medicine, University of Florida, Gainesville, Florida 32611, United States.
Peter A GalieDepartment of Biomedical Engineering, Rowan University, Glassboro, New Jersey 08028, United States.
Rowan University · USUniversity of Florida · US

Funding

Role of Patrolling Monocytes in Cerebral Vascular Repair during HIV/Substance AbuseK01DA046308 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI ANDREWS, ALLISON MICHELLE · 2019 to 2023
$749k
NIDA NIH HHS K01 DA046308
6 · The paper itself

Abstract

Most in vitro models use culture medium to apply fluid shear stress to endothelial cells, which does not capture the interaction between blood and endothelial cells. Here, we describe a new system to characterize whole blood flow through a 3D-printed, endothelialized vascular topology that induces flow separation at a bifurcation. Drag-reducing polymers, which have been previously studied as a potential therapy to reduce the pressure drop across the vascular bed, are evaluated for their effect on mitigating the disturbed flow. Polymer concentrations of 1000 ppm prevented recirculation and disturbed flow at the wall. Proteomic analysis of plasma collected from whole blood recirculated through the vascularized channel with and without drag-reducing polymers provides insight into the effects of flow regimes on levels of proteins indicative of the endothelial-blood interaction. The results indicate that blood flow alters proteins associated with coagulation, inflammation, and other processes. Overall, these proof-of-concept experiments demonstrate the importance of using whole blood flow to study the endothelial response to perfusion.

Indexed as

Endothelial CellsPolymersHemodynamicsPrinting, Three-DimensionalProteomicsStress, MechanicalPolymersbioprintingblood-enothelial interactionshemodynamics

Identifiers

PMID38488736
PMCPMC10982934
OpenAlexW4392845947

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.