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Wet‐Spinning of Biocompatible Core–Shell Polyelectrolyte Complex Fibers for Tissue Engineering
Author(s) -
Cui Qing,
Bell Daniel Josef,
Rauer Sebastian Bernhard,
Wessling Matthias
Publication year - 2020
Publication title -
advanced materials interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.671
H-Index - 65
ISSN - 2196-7350
DOI - 10.1002/admi.202000849
Subject(s) - polyelectrolyte , materials science , spinning , ultimate tensile strength , chemical engineering , polystyrene sulfonate , chitosan , composite material , fiber , synthetic fiber , electrospinning , polymer , engineering , pedot:pss
Polyelectrolyte complex fibers (PEC fibers) have great potential with regard to biomedical applications as they can be fabricated from biocompatible and water‐soluble polyelectrolytes under mild process conditions. The present publication describes a novel method for the continuous fabrication of PEC fibers in a water‐based wet‐spinning process by interfacial complexation within a core–shell spinneret. This process combines the robustness and flexibility of nonsolvent‐induced phase separation (NIPS) spinning processes conventionally used in the membrane industry with the complexation between oppositely charged polyelectrolytes. The produced fibers demonstrate a core–shell structure with a low‐density core and a highly porous polyelectrolyte complex shell of ≈800 μm diameter. In the case of chitosan and polystyrene sulfonate (PSS), mechanical fiber properties could be enhanced by doping the PSS with poly(ethylene oxide) (PEO). The resulting CHI/PSS‐PEO fibers present a Young modulus of 3.78 GPa and a tensile strength of 165 MPa, which is an excellent combination of elongation at break and break stress compared to literature. The suitability of the CHI/PSS‐PEO fibers as a scaffold for cell culture applications is verified by a four‐day cultivation of human HeLa cells on PEO‐reinforced fibers with a subsequent analysis of cell viability by fluorescence‐based live/dead assay.
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