Biomaterials for Local, Controlled Drug Delivery to the Injured Spinal Cord

Affecting approximately 17,000 new people each year, spinal cord injury (SCI) is a devastating injury that leads to permanent paraplegia or tetraplegia. Current pharmacological approaches are limited in their ability to ameliorate this injury pathophysiology, as many are not delivered locally, for a...

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Main Authors: Alexis M. Ziemba, Ryan J. Gilbert
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-05-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fphar.2017.00245/full
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spelling doaj-5540c0713c0341899692a4b76283a7532020-11-25T00:02:48ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122017-05-01810.3389/fphar.2017.00245259505Biomaterials for Local, Controlled Drug Delivery to the Injured Spinal CordAlexis M. ZiembaRyan J. GilbertAffecting approximately 17,000 new people each year, spinal cord injury (SCI) is a devastating injury that leads to permanent paraplegia or tetraplegia. Current pharmacological approaches are limited in their ability to ameliorate this injury pathophysiology, as many are not delivered locally, for a sustained duration, or at the correct injury time point. With this review, we aim to communicate the importance of combinatorial biomaterial and pharmacological approaches that target certain aspects of the dynamically changing pathophysiology of SCI. After reviewing the pathophysiology timeline, we present experimental biomaterial approaches to provide local sustained doses of drug. In this review, we present studies using a variety of biomaterials, including hydrogels, particles, and fibers/conduits for drug delivery. Subsequently, we discuss how each may be manipulated to optimize drug release during a specific time frame following SCI. Developing polymer biomaterials that can effectively release drug to target specific aspects of SCI pathophysiology will result in more efficacious approaches leading to better regeneration and recovery following SCI.http://journal.frontiersin.org/article/10.3389/fphar.2017.00245/fullspinal cord injuryinflammationregenerationdrug deliverybiomaterialshydrogels
collection DOAJ
language English
format Article
sources DOAJ
author Alexis M. Ziemba
Ryan J. Gilbert
spellingShingle Alexis M. Ziemba
Ryan J. Gilbert
Biomaterials for Local, Controlled Drug Delivery to the Injured Spinal Cord
Frontiers in Pharmacology
spinal cord injury
inflammation
regeneration
drug delivery
biomaterials
hydrogels
author_facet Alexis M. Ziemba
Ryan J. Gilbert
author_sort Alexis M. Ziemba
title Biomaterials for Local, Controlled Drug Delivery to the Injured Spinal Cord
title_short Biomaterials for Local, Controlled Drug Delivery to the Injured Spinal Cord
title_full Biomaterials for Local, Controlled Drug Delivery to the Injured Spinal Cord
title_fullStr Biomaterials for Local, Controlled Drug Delivery to the Injured Spinal Cord
title_full_unstemmed Biomaterials for Local, Controlled Drug Delivery to the Injured Spinal Cord
title_sort biomaterials for local, controlled drug delivery to the injured spinal cord
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2017-05-01
description Affecting approximately 17,000 new people each year, spinal cord injury (SCI) is a devastating injury that leads to permanent paraplegia or tetraplegia. Current pharmacological approaches are limited in their ability to ameliorate this injury pathophysiology, as many are not delivered locally, for a sustained duration, or at the correct injury time point. With this review, we aim to communicate the importance of combinatorial biomaterial and pharmacological approaches that target certain aspects of the dynamically changing pathophysiology of SCI. After reviewing the pathophysiology timeline, we present experimental biomaterial approaches to provide local sustained doses of drug. In this review, we present studies using a variety of biomaterials, including hydrogels, particles, and fibers/conduits for drug delivery. Subsequently, we discuss how each may be manipulated to optimize drug release during a specific time frame following SCI. Developing polymer biomaterials that can effectively release drug to target specific aspects of SCI pathophysiology will result in more efficacious approaches leading to better regeneration and recovery following SCI.
topic spinal cord injury
inflammation
regeneration
drug delivery
biomaterials
hydrogels
url http://journal.frontiersin.org/article/10.3389/fphar.2017.00245/full
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