Evidence map›Paper›PMID 30519186›Full record

ReviewFrontiers in pharmacology2018

Targeted Delivery of Bioactive Molecules for Vascular Intervention and Tissue Engineering.

Hannah A Strobel, Elisabet I Qendro, Eben Alsberg, Marsha W Rolle

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  10. Evolution of drug-eluting biomedical implants for sustained drug delivery.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2021
    Review
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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

4 authors at 3 institutions in 1 country.

Hannah A StrobelDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, MA, United States.
Elisabet I QendroGraduate School of Biomedical Sciences, University of Massachusetts Medical School, Worcester, MA, United States.
Eben AlsbergDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, United States.
Marsha W RolleDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, MA, United States.
Worcester Polytechnic Institute · USCase Western Reserve University · USUniversity of Massachusetts Chan Medical School · US

Funding

Medical Scientist Training at UMMS Administrative SupplementT32GM107000 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIEFE, CATARINA I. · 2013 to 2022
$4.9M
Engineering a Self-assembled, multi-tissue Tracheal ReplacementR01EB023907 · NIBIB · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ALSBERG, EBEN, ROLLE, MARSHA W · 2017 to 2020
$1.9M
Engineering a functional human intimal hyperplasia modelR15HL137197 · NHLBI · WORCESTER POLYTECHNIC INSTITUTE · PI ROLLE, MARSHA W · 2018 to 2018
$438k
NHLBI NIH HHS R15 HL137197NIBIB NIH HHS R01 EB023907NIGMS NIH HHS T32 GM107000
6 · The paper itself

Abstract

Cardiovascular diseases are the leading cause of death in the United States. Treatment often requires surgical interventions to re-open occluded vessels, bypass severe occlusions, or stabilize aneurysms. Despite the short-term success of such interventions, many ultimately fail due to thrombosis or restenosis (following stent placement), or incomplete healing (such as after aneurysm coil placement). Bioactive molecules capable of modulating host tissue responses and preventing these complications have been identified, but systemic delivery is often harmful or ineffective. This review discusses the use of localized bioactive molecule delivery methods to enhance the long-term success of vascular interventions, such as drug-eluting stents and aneurysm coils, as well as nanoparticles for targeted molecule delivery. Vascular grafts in particular have poor patency in small diameter, high flow applications, such as coronary artery bypass grafting (CABG). Grafts fabricated from a variety of approaches may benefit from bioactive molecule incorporation to improve patency. Tissue engineering is an especially promising approach for vascular graft fabrication that may be conducive to incorporation of drugs or growth factors. Overall, localized and targeted delivery of bioactive molecules has shown promise for improving the outcomes of vascular interventions, with technologies such as drug-eluting stents showing excellent clinical success. However, many targeted vascular drug delivery systems have yet to reach the clinic. There is still a need to better optimize bioactive molecule release kinetics and identify synergistic biomolecule combinations before the clinical impact of these technologies can be realized.

Indexed as

aneurysmdrug deliverydrug eluting stentnanoparticlevascular graftvascular repairvascular tissue engineering

Identifiers

PMID30519186
PMCPMC6259603
OpenAlexW2900952876

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.