Evidence map›Paper›PMID 32636450›Full record

ArticleScientific reports2020

Preparation and modeling of three-layered PCL/PLGA/PCL fibrous scaffolds for prolonged drug release.

Miljan Milosevic, Dusica B Stojanovic, Vladimir Simic, Mirjana Grkovic, Milos Bjelovic, Petar S Uskokovic, Milos Kojic

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  7. Long-Acting Ocular Injectables: Are We Looking In The Right Direction?Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Miljan Milosevic *Bioengineering Research and Development Center BioIRC Kragujevac, Prvoslava Stojanovica 6, Kragujevac, 34000, Serbia.
Dusica B Stojanovic *Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, Belgrade, 11000, Serbia.ORCID http://orcid.org/0000-0001-6308-7586
Vladimir SimicBioengineering Research and Development Center BioIRC Kragujevac, Prvoslava Stojanovica 6, Kragujevac, 34000, Serbia.
Mirjana GrkovicFaculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, Belgrade, 11000, Serbia.
Milos BjelovicDepartment for Minimally Invasive Upper Digestive Surgery, Clinical Center of Serbia, Hospital for Digestive Surgery - First Surgical Hospital, Dr Koste Todorovica 66, Belgrade, 11000, Serbia.
Petar S UskokovicFaculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, Belgrade, 11000, Serbia.
Milos KojicBioengineering Research and Development Center BioIRC Kragujevac, Prvoslava Stojanovica 6, Kragujevac, 34000, Serbia. mkojic42@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The authors present the preparation procedure and a computational model of a three-layered fibrous scaffold for prolonged drug release. The scaffold, produced by emulsion/sequential electrospinning, consists of a poly(D,L-lactic-co-glycolic acid) (PLGA) fiber layer sandwiched between two poly(ε-caprolactone) (PCL) layers. Experimental results of drug release rates from the scaffold are compared with the results of the recently introduced computational finite element (FE) models for diffusive drug release from nanofibers to the three-dimensional (3D) surrounding medium. Two different FE models are used: (1) a 3D discretized continuum and fibers represented by a simple radial one-dimensional (1D) finite elements, and (2) a 3D continuum discretized by composite smeared finite elements (CSFEs) containing the fiber smeared and surrounding domains. Both models include the effects of polymer degradation and hydrophobicity (as partitioning) of the drug at the fiber/surrounding interface. The CSFE model includes a volumetric fraction of fibers and diameter distribution, and is additionally enhanced by using correction function to improve the accuracy of the model. The computational results are validated on Rhodamine B (fluorescent drug l) and other hydrophilic drugs. Agreement with experimental results proves that numerical models can serve as efficient tools for drug release to the surrounding porous medium or biological tissue. It is demonstrated that the introduced three-layered scaffold delays the drug release process and can be used for the time-controlled release of drugs in postoperative therapy.

Indexed as

MethacrylatesPolyestersPolylactic Acid-Polyglycolic Acid CopolymerDrug Delivery SystemsDrug LiberationModels, ChemicalRhodaminesMethacrylatespoly(epsilon-caprolactone) dimethacrylatePolyestersPolylactic Acid-Polyglycolic Acid Copolymerrhodamine BRhodamines

Identifiers

PMID32636450
PMCPMC7341868

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LicenceCC BY
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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.