Drug-delivering nerve conduit improves regeneration in a critical-sized gap.


Journal

Biotechnology and bioengineering
ISSN: 1097-0290
Titre abrégé: Biotechnol Bioeng
Pays: United States
ID NLM: 7502021

Informations de publication

Date de publication:
01 2019
Historique:
received: 22 06 2018
revised: 04 09 2018
accepted: 05 09 2018
pubmed: 20 9 2018
medline: 18 12 2019
entrez: 20 9 2018
Statut: ppublish

Résumé

Autologous nerve grafts are the current "gold standard" for repairing large nerve gaps. However, they cause morbidity at the donor nerve site and only a limited amount of nerve can be harvested. Nerve conduits are a promising alternative to autografts and can act as guidance cues for the regenerating axons, without the need to harvest donor nerve. Separately, it has been shown that localized delivery of GDNF can enhance axon growth and motor recovery. FK506, an FDA approved small molecule, has also been shown to enhance peripheral nerve regeneration. This paper describes the design of a novel hole-based drug delivery apparatus integrated with a polytetrafluoroethylene (PTFE) nerve conduit for controlled local delivery of a protein such as GDNF or a small molecule such as FK506. The PTFE devices were tested in a diffusion chamber, and the bioactivity of the released media was evaluated by measuring neurite growth of dorsal root ganglions (DRGs) exposed to the released drugs. The drug delivering nerve guide was able to release bioactive concentrations of FK506 or GDNF. Following these tests, optimized drug releasing nerve conduits were implanted across 10 mm sciatic nerve gaps in a BL6 yellow fluorescent protein (YFP) mouse model, where they demonstrated significant improvement in muscle mass, compound muscle action potential, and axon myelination in vivo as compared with nerve conduits without the drug. The drug delivery nerve guide could release drug for extended periods of time and enhance axon growth in vitro and in vivo.

Identifiants

pubmed: 30229866
doi: 10.1002/bit.26837
doi:

Substances chimiques

Drug Carriers 0
Glial Cell Line-Derived Neurotrophic Factor 0
Polytetrafluoroethylene 9002-84-0
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

143-154

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Pratima Labroo (P)

Department of Mechanical Engineering, University of Utah, Salt Lake City, Utah.

David Hilgart (D)

Department of Bioengineering, University of Utah, Salt Lake City, Utah.

Brett Davis (B)

Department of Bioengineering, University of Utah, Salt Lake City, Utah.

Christopher Lambert (C)

Department of Mechanical Engineering, University of Utah, Salt Lake City, Utah.

Himanshu Sant (H)

Department of Mechanical Engineering, University of Utah, Salt Lake City, Utah.

Bruce Gale (B)

Department of Mechanical Engineering, University of Utah, Salt Lake City, Utah.

Jill E Shea (JE)

Department of Surgery, University of Utah, Salt Lake City, Utah.

Jayant Agarwal (J)

Department of Surgery, University of Utah, Salt Lake City, Utah.

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Classifications MeSH