Architectured helically coiled scaffolds from elastomeric poly(butylene succinate) (PBS) copolyester via wet electrospinning

Mater Sci Eng C Mater Biol Appl. 2020 Mar:108:110505. doi: 10.1016/j.msec.2019.110505. Epub 2019 Nov 29.

Abstract

Electrospinning is one of the most investigated methods used to produce polymeric fiber scaffolds that mimic the morphology of native extracellular matrix. These structures have been extensively studied in the context of scaffolds for tissue regeneration. However, the compactness of materials obtained by traditional electrospinning, collected as two-dimensional non-woven scaffolds, can limit cell infiltration and tissue ingrowth. In addition, for applications in smooth muscle tissue engineering, highly elastic scaffolds capable of withstanding cyclic mechanical strains without suffering significant permanent deformations are preferred. In order to address these challenges, we report the fabrication of microscale 3D helically coiled scaffolds (referred as 3D-HCS) by wet-electrospinning method, a modification of the traditional electrospinning process in which a coagulation bath (non-solvent system for the electrospun material) is used as the collector. The present study, for the first time, successfully demonstrates the feasibility of using this method to produce various architectures of 3D helically coiled scaffolds (HCS) from segmented copolyester of poly (butylene succinate-co-dilinoleic succinate) (PBS-DLS), a thermoplastic elastomer. We examined the role of process parameters and propose a mechanism for the HCS formation. Fabricated 3D-HCS showed high specific surface area, high porosity, and good elasticity. Further, the marked increase in cell proliferation on 3D-HCS confirmed the suitability of these materials as scaffolds for soft tissue engineering.

Keywords: Coagulation bath collector; Electrospinning; Helically coiled architectures; Poly(butylene succinate)(PBS); Polyester.

MeSH terms

  • Animals
  • Butylene Glycols / chemistry*
  • Cell Line
  • Cell Proliferation
  • Cell Survival
  • Elasticity
  • Elastomers*
  • Electrochemistry / methods*
  • Imaging, Three-Dimensional
  • Mice
  • Microscopy, Electron, Scanning
  • Polyesters / chemistry*
  • Polymers / chemistry*
  • Porosity
  • Stress, Mechanical
  • Surface Properties
  • Tissue Engineering / methods
  • Tissue Scaffolds*
  • X-Ray Microtomography

Substances

  • Butylene Glycols
  • Elastomers
  • Polyesters
  • Polymers
  • bionole