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Hydrogel-based local drug delivery strategies for spinal cord repair

Spinal cord injury results in significant loss of motor, sensory, and autonomic functions. Although a wide range of therapeutic agents have been shown to attenuate secondary injury or promote regeneration/repair in animal models of spinal cord injury, clinical translation of these strategies has bee...

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Detalles Bibliográficos
Autores principales: Shultz, Robert B., Zhong, Yinghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896229/
https://www.ncbi.nlm.nih.gov/pubmed/32859771
http://dx.doi.org/10.4103/1673-5374.290882
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author Shultz, Robert B.
Zhong, Yinghui
author_facet Shultz, Robert B.
Zhong, Yinghui
author_sort Shultz, Robert B.
collection PubMed
description Spinal cord injury results in significant loss of motor, sensory, and autonomic functions. Although a wide range of therapeutic agents have been shown to attenuate secondary injury or promote regeneration/repair in animal models of spinal cord injury, clinical translation of these strategies has been limited, in part due to difficulty in safely and effectively achieving therapeutic concentrations in the injured spinal cord tissue. Hydrogel-based drug delivery systems offer unique opportunities to locally deliver drugs to the injured spinal cord with sufficient dose and duration, while avoiding deleterious side effects associated with systemic drug administration. Such local drug delivery systems can be readily fabricated from biocompatible and biodegradable materials. In this review, hydrogel-based strategies for local drug delivery to the injured spinal cord are extensively reviewed, and recommendations are made for implementation.
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spelling pubmed-78962292021-02-24 Hydrogel-based local drug delivery strategies for spinal cord repair Shultz, Robert B. Zhong, Yinghui Neural Regen Res Review Spinal cord injury results in significant loss of motor, sensory, and autonomic functions. Although a wide range of therapeutic agents have been shown to attenuate secondary injury or promote regeneration/repair in animal models of spinal cord injury, clinical translation of these strategies has been limited, in part due to difficulty in safely and effectively achieving therapeutic concentrations in the injured spinal cord tissue. Hydrogel-based drug delivery systems offer unique opportunities to locally deliver drugs to the injured spinal cord with sufficient dose and duration, while avoiding deleterious side effects associated with systemic drug administration. Such local drug delivery systems can be readily fabricated from biocompatible and biodegradable materials. In this review, hydrogel-based strategies for local drug delivery to the injured spinal cord are extensively reviewed, and recommendations are made for implementation. Wolters Kluwer - Medknow 2020-08-24 /pmc/articles/PMC7896229/ /pubmed/32859771 http://dx.doi.org/10.4103/1673-5374.290882 Text en Copyright: © 2021 Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review
Shultz, Robert B.
Zhong, Yinghui
Hydrogel-based local drug delivery strategies for spinal cord repair
title Hydrogel-based local drug delivery strategies for spinal cord repair
title_full Hydrogel-based local drug delivery strategies for spinal cord repair
title_fullStr Hydrogel-based local drug delivery strategies for spinal cord repair
title_full_unstemmed Hydrogel-based local drug delivery strategies for spinal cord repair
title_short Hydrogel-based local drug delivery strategies for spinal cord repair
title_sort hydrogel-based local drug delivery strategies for spinal cord repair
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896229/
https://www.ncbi.nlm.nih.gov/pubmed/32859771
http://dx.doi.org/10.4103/1673-5374.290882
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