Evidence map›Paper›PMID 39564556›Full record

ArticleIEEE open journal of engineering in medicine and biology2025

A Strategy for the In-Silico Assessment of Drug Eluting Stents: A Comparative Study for the Evaluation of Retinoic Acid as a Novel Drug Candidate for Drug Eluting Stents.

Dimitrios S Pleouras, Vasileios S Loukas, Georgia Karanasiou, Christos Katsouras, Arsen Semertzioglou, Anargyros N Moulas, Lambros K Michalis, Dimitrios I Fotiadis

Abstract read
In one paragraph

Article in IEEE open journal of engineering in medicine and biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Dimitrios S PleourasUnit of Medical Technology and Intelligent Information Systems, Department of Materials Science and EngineeringUniversity of Ioannina GR45110 Ioannina Greece.ORCID https://orcid.org/0000-0002-8000-8218
Vasileios S LoukasUnit of Medical Technology and Intelligent Information Systems, Department of Materials Science and EngineeringUniversity of Ioannina GR45110 Ioannina Greece.ORCID https://orcid.org/0000-0001-6390-884X
Georgia KaranasiouUnit of Medical Technology and Intelligent Information Systems, Department of Materials Science and EngineeringUniversity of Ioannina GR45110 Ioannina Greece.ORCID https://orcid.org/0000-0001-9478-0375
Christos KatsourasDepartment of Cardiology, Medical SchoolUniversity of Ioannina GR45110 Ioannina Greece.ORCID https://orcid.org/0000-0001-7638-9217
Arsen SemertzioglouRontis Corporation S.A. GR15125 Athens Greece.ORCID https://orcid.org/0009-0003-0388-8594
Anargyros N MoulasDepartment of Agricultural TechnologyUniversity of Thessaly GR35100 Lamia Greece.ORCID https://orcid.org/0000-0002-4681-6174
Lambros K MichalisBiomedical Research Institute - FORTHUniversity Campus of Ioannina GR45110 Ioannina Greece.ORCID https://orcid.org/0000-0001-8834-4462
Dimitrios I FotiadisUnit of Medical Technology and Intelligent Information Systems, Department of Materials Science and EngineeringUniversity of Ioannina GR45110 Ioannina Greece.ORCID https://orcid.org/0000-0002-5987-9350

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work, a methodology for the in-silico evaluation of drug eluting stents (DES) is presented. A stent model developed by Rontis S.A. has been employed. For modeling purposes two different stent parts have been considered: the metal core and the coating. For the arterial models, we used animal specific imaging data and realistic geometries were reconstructed which were used as input to the drug-delivery model. More specifically, optical coherence tomography (OCT) imaging data from two coney iliac arterial segments were 3D reconstructed, and the preprocessed 3D stent was deployed in-silico. The deformed geometries of the in-silico deployed stents and the dilated arterial segments were used as input to the drug elution model. The same reconstructed arteries were used in three different cases: (i) Case A. The coatings contain retinoic acid at an initial concentration 49.2% w/w. (ii) Case B. The coatings contain retinoic acid at an initial concentration 1% w/w. (iii) Case C. The coatings contain sirolimus at an initial concentration 0.85% w/w. In each case, two different coatings were examined: (a) polylactic acid and (b) polylactic-co-glycolic acid. The results proved that retinoic acid is a very promising drug candidate for DES due to its binding time to the smooth muscle cells of the arterial wall that exceeds the corresponding time of sirolimus, while being non-toxic to the smooth muscle cells.

Indexed as

computational modelingcontrolled release. retinoic acidDrug eluting stentssirolimus

Identifiers

PMID39564556
PMCPMC11573404

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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.