Evidence map›Paper›PMID 36771970›Full record

ArticlePolymers2023

Accelerated Degradation of Poly-ε-caprolactone Composite Scaffolds for Large Bone Defects.

Evangelos Daskalakis, Mohamed H Hassan, Abdalla M Omar, Anil A Acar, Ali Fallah, Glen Cooper, Andrew Weightman, Gordon Blunn, Bahattin Koc, Paulo Bartolo

Abstract read
In one paragraph

Article in Polymers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  12. 3D printed OActa biomaterialia · 2024
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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

10 authors.

Evangelos DaskalakisSchool of Mechanical, Aerospace and Civil Engineering, University of Manchester, Manchester M13 9PL, UK.ORCID 0000-0003-3855-5442
Mohamed H HassanSchool of Mechanical, Aerospace and Civil Engineering, University of Manchester, Manchester M13 9PL, UK.ORCID 0000-0002-0832-8559
Abdalla M OmarSchool of Mechanical, Aerospace and Civil Engineering, University of Manchester, Manchester M13 9PL, UK.
Anil A AcarIntegrated Manufacturing Technologies Research and Application Center, Sabanci University, Tuzla 34956, Istanbul, Turkey.
Ali FallahIntegrated Manufacturing Technologies Research and Application Center, Sabanci University, Tuzla 34956, Istanbul, Turkey.ORCID 0000-0002-7744-4246
Glen CooperSchool of Mechanical, Aerospace and Civil Engineering, University of Manchester, Manchester M13 9PL, UK.ORCID 0000-0002-9568-8973
Andrew WeightmanSchool of Mechanical, Aerospace and Civil Engineering, University of Manchester, Manchester M13 9PL, UK.ORCID 0000-0001-7232-4942
Gordon BlunnSchool of Pharmacy and Biomedical Sciences, University of Portsmouth, Portsmouth PO1 2DT, UK.ORCID 0000-0003-2141-7385
Bahattin KocIntegrated Manufacturing Technologies Research and Application Center, Sabanci University, Tuzla 34956, Istanbul, Turkey.ORCID 0000-0001-9073-8516
Paulo BartoloSchool of Mechanical, Aerospace and Civil Engineering, University of Manchester, Manchester M13 9PL, UK.

Funding

Engineering and Physical Sciences Research Council EP/R01513/1
6 · The paper itself

Abstract

This research investigates the accelerated hydrolytic degradation process of both anatomically designed bone scaffolds with a pore size gradient and a rectangular shape (biomimetically designed scaffolds or bone bricks). The effect of material composition is investigated considering poly-ε-caprolactone (PCL) as the main scaffold material, reinforced with ceramics such as hydroxyapatite (HA), β-tricalcium phosphate (TCP) and bioglass at a concentration of 20 wt%. In the case of rectangular scaffolds, the effect of pore size (200 μm, 300 μm and 500 μm) is also investigated. The degradation process (accelerated degradation) was investigated during a period of 5 days in a sodium hydroxide (NaOH) medium. Degraded bone bricks and rectangular scaffolds were measured each day to evaluate the weight loss of the samples, which were also morphologically, thermally, chemically and mechanically assessed. The results show that the PCL/bioglass bone brick scaffolds exhibited faster degradation kinetics in comparison with the PCL, PCL/HA and PCL/TCP bone bricks. Furthermore, the degradation kinetics of rectangular scaffolds increased by increasing the pore size from 500 μm to 200 μm. The results also indicate that, for the same material composition, bone bricks degrade slower compared with rectangular scaffolds. The scanning electron microscopy (SEM) images show that the degradation process was faster on the external regions of the bone brick scaffolds (600 μm pore size) compared with the internal regions (200 μm pore size). The thermal gravimetric analysis (TGA) results show that the ceramic concentration remained constant throughout the degradation process, while differential scanning calorimetry (DSC) results show that all scaffolds exhibited a reduction in crystallinity (Xc), enthalpy (Δm) and melting temperature (Tm) throughout the degradation process, while the glass transition temperature (Tg) slightly increased. Finally, the compression results show that the mechanical properties decreased during the degradation process, with PCL/bioglass bone bricks and rectangular scaffolds presenting higher mechanical properties with the same design in comparison with the other materials.

Indexed as

3D printingadditive manufacturingbiomaterialsdegradation process

Identifiers

PMID36771970
PMCPMC9921763

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Registered trials

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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.