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Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment

Peripheral nerve injuries account for roughly 3% of all trauma patients with over 900,000 repair procedures annually in the US. Of all extremity peripheral nerve injuries, 51% require nerve repair with a transected gap. The current gold-standard treatment for peripheral nerve injuries, autograft rep...

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Autores principales: Manoukian, Ohan S., Rudraiah, Swetha, Arul, Michael R., Bartley, Jenna M., Baker, Jiana T., Yu, Xiaojun, Kumbar, Sangamesh G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907220/
https://www.ncbi.nlm.nih.gov/pubmed/33718669
http://dx.doi.org/10.1016/j.bioactmat.2021.02.016
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author Manoukian, Ohan S.
Rudraiah, Swetha
Arul, Michael R.
Bartley, Jenna M.
Baker, Jiana T.
Yu, Xiaojun
Kumbar, Sangamesh G.
author_facet Manoukian, Ohan S.
Rudraiah, Swetha
Arul, Michael R.
Bartley, Jenna M.
Baker, Jiana T.
Yu, Xiaojun
Kumbar, Sangamesh G.
author_sort Manoukian, Ohan S.
collection PubMed
description Peripheral nerve injuries account for roughly 3% of all trauma patients with over 900,000 repair procedures annually in the US. Of all extremity peripheral nerve injuries, 51% require nerve repair with a transected gap. The current gold-standard treatment for peripheral nerve injuries, autograft repair, has several shortcomings. Engineered constructs are currently only suitable for short gaps or small diameter nerves. Here, we investigate novel nerve guidance conduits with aligned microchannel porosity that deliver sustained-release of neurogenic 4-aminopyridine (4-AP) for peripheral nerve regeneration in a critical-size (15 mm) rat sciatic nerve transection model. The results of functional walking track analysis, morphometric evaluations of myelin development, and histological assessments of various markers confirmed the equivalency of our drug-conduit with autograft controls. Repaired nerves showed formation of thick myelin, presence of S100 and neurofilament markers, and promising functional recovery. The conduit's aligned microchannel architecture may play a vital role in physically guiding axons for distal target reinnervation, while the sustained release of 4-AP may increase nerve conduction, and in turn synaptic neurotransmitter release and upregulation of critical Schwann cell neurotrophic factors. Overall, our nerve construct design facilitates efficient and efficacious peripheral nerve regeneration via a drug delivery system that is feasible for clinical applications.
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spelling pubmed-79072202021-03-12 Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment Manoukian, Ohan S. Rudraiah, Swetha Arul, Michael R. Bartley, Jenna M. Baker, Jiana T. Yu, Xiaojun Kumbar, Sangamesh G. Bioact Mater Article Peripheral nerve injuries account for roughly 3% of all trauma patients with over 900,000 repair procedures annually in the US. Of all extremity peripheral nerve injuries, 51% require nerve repair with a transected gap. The current gold-standard treatment for peripheral nerve injuries, autograft repair, has several shortcomings. Engineered constructs are currently only suitable for short gaps or small diameter nerves. Here, we investigate novel nerve guidance conduits with aligned microchannel porosity that deliver sustained-release of neurogenic 4-aminopyridine (4-AP) for peripheral nerve regeneration in a critical-size (15 mm) rat sciatic nerve transection model. The results of functional walking track analysis, morphometric evaluations of myelin development, and histological assessments of various markers confirmed the equivalency of our drug-conduit with autograft controls. Repaired nerves showed formation of thick myelin, presence of S100 and neurofilament markers, and promising functional recovery. The conduit's aligned microchannel architecture may play a vital role in physically guiding axons for distal target reinnervation, while the sustained release of 4-AP may increase nerve conduction, and in turn synaptic neurotransmitter release and upregulation of critical Schwann cell neurotrophic factors. Overall, our nerve construct design facilitates efficient and efficacious peripheral nerve regeneration via a drug delivery system that is feasible for clinical applications. KeAi Publishing 2021-02-22 /pmc/articles/PMC7907220/ /pubmed/33718669 http://dx.doi.org/10.1016/j.bioactmat.2021.02.016 Text en © 2021 [The Author/The Authors] http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Manoukian, Ohan S.
Rudraiah, Swetha
Arul, Michael R.
Bartley, Jenna M.
Baker, Jiana T.
Yu, Xiaojun
Kumbar, Sangamesh G.
Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment
title Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment
title_full Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment
title_fullStr Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment
title_full_unstemmed Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment
title_short Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment
title_sort biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: in vivo structural and functional assessment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907220/
https://www.ncbi.nlm.nih.gov/pubmed/33718669
http://dx.doi.org/10.1016/j.bioactmat.2021.02.016
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