Biofunctionalized PEDOT-coated microfibers for the treatment of spinal cord injury.

Biomaterials

Neural Repair and Biomaterials Laboratory, Hospital Nacional de Parapléjicos (SESCAM), Finca La Peraleda s/n, 45071 Toledo, Spain. Electronic address:

Published: May 2016

AI Article Synopsis

  • PEDOT-MFs, coated carbon microfibers, show potential for neuroprostheses and neural repair by integrating well with spinal cord tissue and reducing scarring after injury.
  • Functionalizing these microfibers with a combination of PLL, heparin, bFGF, and fibronectin enhances cellular interaction and promotes healing, compared to non-functionalized microfibers which induce inflammation and damage.
  • The study highlights the benefits of using biofunctionalized PEDOT-MFs in developing treatments for spinal cord injuries, supporting their role in neuro-electronic interfaces and tissue regeneration.

Article Abstract

Poly(3, 4-ethylenedioxythiophene)-coated carbon microfibers (PEDOT-MFs) hold promise for developing advanced neuroprostheses and neural repair devices. We investigated the chronic cellular responses to PEDOT-MFs implanted into the uninjured and the transected rat spinal cord, and compared the effects of polymer surface biofunctionalization with covalently attached polylysine (PLL) or a multimolecular complex of PLL, heparin, basic fibroblast growth factor (bFGF), and fibronectin. An alginate gel was used to facilitate microfiber implantation and reduce connective tissue scarring after spinal cord injury (SCI). PLL/heparin/bFGF/fibronectin-functionalized PEDOT-MFs showed excellent integration within the uninjured and injured spinal cord, frequently establishing contact with neuronal somas, axons, dendrites and glial cells, accompanied by very little or absent scarring response. On the contrary, non-functionalized and PLL-functionalized microfibers provoked inflammation and fibrosis with loss of neural elements in the surrounding tissue. Within the lesion, the PEDOT-MFs by themselves facilitated longitudinal alignment of migratory cells and growing axons, and their modification with PLL/heparin/bFGF/fibronectin promoted tissue healing, enhancing blood vessel formation and axonal regeneration without increasing inflammation. These results support the incorporation of biofunctionalized electroconducting microfibers in neuro-electronic interfaces and lesion-bridging systems for the treatment of SCI.

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Source
http://dx.doi.org/10.1016/j.biomaterials.2016.02.037DOI Listing

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