Poly(3,4-ethylenedioxythiophene) nanoparticle and poly(ɛ-caprolactone) electrospun scaffold characterization for skeletal muscle regeneration

Injuries to peripheral nerves and/or skeletal muscle can cause scar tissue formation and loss of function. The focus of this article is the creation of a conductive, biocompatible scaffold with appropriate mechanical properties to regenerate skeletal muscle. Poly(3,4‐ethylenedioxythiophene) (PEDOT)...

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Veröffentlicht in:Journal of biomedical materials research. Part A 2015-11, Vol.103 (11), p.3633-3641
Hauptverfasser: McKeon-Fischer, Kristin D., Browe, Daniel P., Olabisi, Ronke M., Freeman, Joseph W.
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Sprache:eng
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Zusammenfassung:Injuries to peripheral nerves and/or skeletal muscle can cause scar tissue formation and loss of function. The focus of this article is the creation of a conductive, biocompatible scaffold with appropriate mechanical properties to regenerate skeletal muscle. Poly(3,4‐ethylenedioxythiophene) (PEDOT) nanoparticles (Np) were electrospun with poly(ɛ‐caprolactone) (PCL) to form conductive scaffolds. During electrospinning, ribboning, larger fiber diameters, and unaligned scaffolds were observed with increasing PEDOT amounts. To address this, PEDOT Np were sonicated prior to electrospinning, which resulted in decreased conductivity and increased mechanical properties. Multi‐walled carbon nanotubes (MWCNT) were added to the 1:2 solution in an effort to increase conductivity. However, the addition of MWCNT had little effect on scaffold conductivity, and the elastic modulus and yield stress of the scaffold increased as a result. Rat muscle cells attached and were active on the 1–10, 1–2, 3–4, and 1–1 PCL‐PEDOT scaffolds; however, the 3–4 scaffolds had the lowest level of metabolic activity. Although the scaffolds were cytocompatible, further development of the fabrication method is necessary to produce more highly aligned scaffolds capable of promoting skeletal muscle cell alignment and eventual regeneration. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 3633–3641, 2015.
ISSN:1549-3296
1552-4965
DOI:10.1002/jbm.a.35481