Cited by 22Electrospun Nanofibers in Biomedical Applicationsbiodegradable polymer synthesis and propertiesBone Tissue Engineering Materials

Comparison and characterization of different polyester nano/micro fibres for use in tissue engineering applications

Mikes, Petr, Horakova, Jana, Saman, Ales, Vejsadova, Lucie, Topham, Paul, Punyodom, Winita, Dumklang, Manita, Jencova, Vera·2021·Journal of Industrial Textiles

Abstract

The study focuses on a comparison of the electrospinning of various polylactide and polycaprolactone (PLCL) copolymers and poly-L-lactide (PLLA) and polycaprolactone (PCL) homopolymers. The chemical characterisation, electrospinnability, fibrous morphology, degradation rate and interactions with fibroblasts were assessed with respect to copolymers and homopolymers with both lower (around 50,000) and higher (around 95,000) molecular weights. The research investigated commercially available as well as synthesised copolymers. The results revealed that the electrospinnability of polymeric solutions depends on both the molecular weight and the PLA/PCL ratio in the final copolymer. It was determined that PLCL copolymers with a higher content of PCL (≥20%) were not spinnable via the electrospinning process. With the exception of PCL, the resulting fibrous materials were found to be homogeneous and with fibre diameters of slightly more than 1 µm with respect to both the tested molecular weights. The degradation rate was tested under simulation conditions via the utilisation of the lipase and Proteinase K enzymes. The degree of degradation was found to depend on the molecular weight, the crystallinity of the polymer and the specificity of the enzyme applied. While lipase was responsible for the degradation of the PCL polymer, it exerted a minor impact on the PLLA and the copolymers. Proteinase K degraded all the tested polymers with a higher specificity towards PLLA and the PLCL copolymers. All the tested polymers were affected by the surface erosion degradation process via fibrous morphology changes and mass loss with no accompanying shift in the molar mass. The electrospun PLLA materials supported both fibroblast adhesion and proliferation. All the tested materials were determined to be cytocompatible with 3T3 mouse fibroblasts.

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Crossref · 10.1177/1528083719848155

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  • By adjusting the ratio of L-lactide to ε-caprolactone and the molecular weight of synthesized PLCL, the degradation time of PLCL can be flexibly adjusted from weeks to years.

    “By adjusting the ratio of L-lactide to ε-caprolactone and the molecular weight of the synthesized PLCL, the degradation time of PLCL can be flexibly adjusted from weeks to years [42].”

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Authors
Mikes, P., Horakova, J., Saman, A., Vejsadova, L., Topham, P., Punyodom, W., Dumklang, M., & Jencova, V.
Affiliations
  • Technical University of Liberec, Liberec, Czech Republic
  • Technical University of Liberec (CZ)
  • Aston University (GB)
  • Chiang Mai University (TH)
  • Rajamangala University of Technology Lanna (TH)
Venue
Journal of Industrial Textiles
Published
2019-05-08
Volume
50
Issue
6
Pages
870-890
ISSN
  • 0093-4658 (ISSN-L)
  • 1528-0837
  • 1530-8057
OpenAlex
W2944709028
Cited by
22
References
35
Citations by year
2026: 4 · 2025: 1 · 2024: 1 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 4 · 2019: 3
FWCI
0.92
Type
journal article
Language
en
Open access
closed
Locations
Journal of Industrial Textiles (publishedVersion)
Funders
Grantová Agentura Ćeské Republiky (GACR 17-02448S)
Topics
  • Physical Sciences › Materials Science › Biomaterials › Electrospun Nanofibers in Biomedical Applications
  • Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
Keywords
electrospinning, polylactic acid, polycaprolactone, poly(L-lactic acid), electrospinnability, molecular weight, copolymer ratio, enzyme degradation, lipase, proteinase K, surface erosion, crystallinity, fibroblast adhesion, fibroblast proliferation, 3T3 fibroblasts, cytocompatibility, tissue engineering scaffolds

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