Influence of the Fabrication Accuracy of Hot-Embossed PCL Scaffolds on Cell Growths.

cell viability demolding force hot embossing microstructured scaffolds polycaprolactone

Journal

Frontiers in bioengineering and biotechnology
ISSN: 2296-4185
Titre abrégé: Front Bioeng Biotechnol
Pays: Switzerland
ID NLM: 101632513

Informations de publication

Date de publication:
2020
Historique:
received: 29 08 2019
accepted: 29 01 2020
entrez: 3 3 2020
pubmed: 3 3 2020
medline: 3 3 2020
Statut: epublish

Résumé

Polycaprolactone (PCL) is a biocompatible and biodegradable polymer widely used for the realization of 3D scaffold for tissue engineering applications. The hot embossing technique (HE) allows the obtainment of PCL scaffolds with a regular array of micro pillars on their surface. The main drawback affecting this kind of micro fabrication process is that such structural superficial details can be damaged when detaching the replica from the mold. Therefore, the present study has focused on the optimization of the HE processes through the development of an analytical model for the prediction of the demolding force as a function of temperature. This model allowed calculating the minimum demolding force to obtain regular micropillars without defects. We demonstrated that the results obtained by the analytical model agree with the experimental data. To address the importance of controlling accurately the fabricated microstructures, we seeded on the PCL scaffolds human stromal cell line (HS-5) and monocytic leukemia cell line (THP-1) to evaluate how the presence of regular or deformed pillars affect cells viability.

Identifiants

pubmed: 32117950
doi: 10.3389/fbioe.2020.00084
pmc: PMC7033415
doi:

Types de publication

Journal Article

Langues

eng

Pagination

84

Informations de copyright

Copyright © 2020 Limongi, Dattola, Botta, Coluccio, Candeloro, Cucè, Scopacasa, Gallo Cantafio, Critello, Pullano, Fiorillo, Tagliaferri, Tassone, Lamanna, Di Fabrizio and Perozziello.

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Auteurs

Tania Limongi (T)

Department of Applied Science and Technology, Polytechnic University of Turin, Turin, Italy.

Elisabetta Dattola (E)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.

Cirino Botta (C)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Maria Laura Coluccio (ML)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Patrizio Candeloro (P)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Maria Cucè (M)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Bernadette Scopacasa (B)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Maria Eugenia Gallo Cantafio (ME)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Costantino Davide Critello (CD)

Department of Health Sciences, University of Magna Graecia, Catanzaro, Italy.

Salvatore Andrea Pullano (SA)

Department of Health Sciences, University of Magna Graecia, Catanzaro, Italy.

Antonino S Fiorillo (AS)

Department of Health Sciences, University of Magna Graecia, Catanzaro, Italy.

Pierosandro Tagliaferri (P)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Pierfrancesco Tassone (P)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Ernesto Lamanna (E)

Department of Health Sciences, University of Magna Graecia, Catanzaro, Italy.

Enzo Di Fabrizio (E)

Department of Applied Science and Technology, Polytechnic University of Turin, Turin, Italy.
King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.

Gerardo Perozziello (G)

Department of Experimental and Clinical Medicine, University of Magna Graecia, Catanzaro, Italy.

Classifications MeSH