Evidence map›Paper›PMID 35268968›Full record

ArticleMaterials (Basel, Switzerland)2022

Modified Histopathological Protocol for Poly-ɛ-Caprolactone Scaffolds Preserving Their Trabecular, Honeycomb-like Structure.

Tomasz Dębski, Juliusz Wysocki, Katarzyna Siennicka, Jakub Jaroszewicz, Karol Szlązak, Wojciech Święszkowski, Zygmunt Pojda

Abstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Histological Processing of Scaffolds: Challenges and Solutions.Journal of functional biomaterials · 2025
    Review
  3. Review
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

7 authors.

Tomasz DębskiDepartment of Regenerative Medicine, Maria Sklodowska-Curie National Research Institute of Oncology, Wilhelma Konrada Roentgena 5, 02-781 Warsaw, Poland.ORCID 0000-0003-4924-2177
Juliusz WysockiDepartment of Regenerative Medicine, Maria Sklodowska-Curie National Research Institute of Oncology, Wilhelma Konrada Roentgena 5, 02-781 Warsaw, Poland.
Katarzyna SiennickaDepartment of Regenerative Medicine, Maria Sklodowska-Curie National Research Institute of Oncology, Wilhelma Konrada Roentgena 5, 02-781 Warsaw, Poland.ORCID 0000-0002-1612-939X
Jakub JaroszewiczMaterials Design Division, Faculty of Materials Science and Engineering, Warsaw University of Technology, Woloska 141, 02-507 Warsaw, Poland.
Karol SzlązakMaterials Design Division, Faculty of Materials Science and Engineering, Warsaw University of Technology, Woloska 141, 02-507 Warsaw, Poland.
Wojciech ŚwięszkowskiMaterials Design Division, Faculty of Materials Science and Engineering, Warsaw University of Technology, Woloska 141, 02-507 Warsaw, Poland.
Zygmunt PojdaDepartment of Regenerative Medicine, Maria Sklodowska-Curie National Research Institute of Oncology, Wilhelma Konrada Roentgena 5, 02-781 Warsaw, Poland.ORCID 0000-0001-5562-4433

Funding

European Union Grant POIG.01.01.02-00-022/09National Centre for Research and Development STRATEGMED 3/306888/3/NCBR/2017
6 · The paper itself

Abstract

Poly-ɛ-caprolactone (PCL) is now widely studied in relation to the engineering of bone, cartilage, tendons, and other tissues. Standard histological protocols can destroy the carefully created trabecular and honeycomb-like architecture of PCL scaffolds, and could lead to scaffold fibers swelling, resulting in the displacement or compression of tissues inside the scaffold. The aim of this study was to modify a standard histopathological protocol for PCL scaffold preparation and evaluate it on porous cylindrical PCL scaffolds in a rat model. In 16 inbred Wag rats, 2 PCL scaffolds were implanted subcutaneously to both inguinal areas. Two months after implantation, harvested scaffolds were first subjected to μCT imaging, and then to histopathological analysis with standard (left inguinal area) and modified histopathological protocols (right inguinal area). To standardize the results, soft tissue percentages (STPs) were calculated on scaffold cross-sections obtained from both histopathological protocols and compared with corresponding µCT cross-sections. The modified protocol enabled the assessment of almost 10× more soft tissues on the scaffold cross-section than the standard procedure. Moreover, STP was only 1.5% lower than in the corresponding µCT cross-sections assessed before the histopathological procedure. The presented modification of the histopathological protocol is cheap, reproducible, and allows for a comprehensive evaluation of PCL scaffolds while maintaining their trabecular, honeycomb-like structure on cross-sections.

Indexed as

full cross-section of scaffoldhistopathological protocolPCLscaffoldscaffold architecture preservation

Identifiers

PMID35268968
PMCPMC8911251

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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.