Cargando…
Bioengineered Zinc Oxide Nanoparticle-Loaded Hydrogel for Combinative Treatment of Spinal Cord Transection
Spinal cord injury (SCI) is one of the most destructive diseases. The neuroinflammation microenvironment needs comprehensive mitigation of damages. Thus, regulation of local, microenvironment drugs could be a potential effective treatment. However, clinical studies on SCI with common treatment have...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793849/ https://www.ncbi.nlm.nih.gov/pubmed/35096792 http://dx.doi.org/10.3389/fbioe.2021.796361 |
_version_ | 1784640696981913600 |
---|---|
author | Lin, Sen Zhao, Hao-sen Xu, Chang Zhou, Zi-peng Wang, Da-hao Chen, Shu-rui Mei, Xi-fan |
author_facet | Lin, Sen Zhao, Hao-sen Xu, Chang Zhou, Zi-peng Wang, Da-hao Chen, Shu-rui Mei, Xi-fan |
author_sort | Lin, Sen |
collection | PubMed |
description | Spinal cord injury (SCI) is one of the most destructive diseases. The neuroinflammation microenvironment needs comprehensive mitigation of damages. Thus, regulation of local, microenvironment drugs could be a potential effective treatment. However, clinical studies on SCI with common treatment have reported it to cause systemic toxicity and side effects. Zinc oxide nanoparticles (ZnONPs) have been widely reported to have satisfying anti-inflammation function. Furthermore, green synthesis procedures can improve the capability and possible utilization of ZnONPs. However, the efficient administration and underlying mechanism of ZnONPs in SCI treatment remain unclear. Herein, an innovative approach was built by utilizing ZnONPs loaded in a skeletal muscle-derived adhesive hydrogel (ZnONPs-Gel). Different from the systemic application of ZnONPs, the local administration of ZnONPs-Gel offered the ZnONPs-loaded extracellular matrix with beneficial biocompatibility to the injured spinal cord, thereby promoting effective function recovery. Mechanistically, the ZnONPs-Gel treatment not only markedly reduced ROS production but also decreased apoptosis in the injured spinal cord. Therefore, the strategy based on local administration of the ZnONPs-Gel in the early stage of SCI may be an effective therapeutic treatment. |
format | Online Article Text |
id | pubmed-8793849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87938492022-01-28 Bioengineered Zinc Oxide Nanoparticle-Loaded Hydrogel for Combinative Treatment of Spinal Cord Transection Lin, Sen Zhao, Hao-sen Xu, Chang Zhou, Zi-peng Wang, Da-hao Chen, Shu-rui Mei, Xi-fan Front Bioeng Biotechnol Bioengineering and Biotechnology Spinal cord injury (SCI) is one of the most destructive diseases. The neuroinflammation microenvironment needs comprehensive mitigation of damages. Thus, regulation of local, microenvironment drugs could be a potential effective treatment. However, clinical studies on SCI with common treatment have reported it to cause systemic toxicity and side effects. Zinc oxide nanoparticles (ZnONPs) have been widely reported to have satisfying anti-inflammation function. Furthermore, green synthesis procedures can improve the capability and possible utilization of ZnONPs. However, the efficient administration and underlying mechanism of ZnONPs in SCI treatment remain unclear. Herein, an innovative approach was built by utilizing ZnONPs loaded in a skeletal muscle-derived adhesive hydrogel (ZnONPs-Gel). Different from the systemic application of ZnONPs, the local administration of ZnONPs-Gel offered the ZnONPs-loaded extracellular matrix with beneficial biocompatibility to the injured spinal cord, thereby promoting effective function recovery. Mechanistically, the ZnONPs-Gel treatment not only markedly reduced ROS production but also decreased apoptosis in the injured spinal cord. Therefore, the strategy based on local administration of the ZnONPs-Gel in the early stage of SCI may be an effective therapeutic treatment. Frontiers Media S.A. 2022-01-13 /pmc/articles/PMC8793849/ /pubmed/35096792 http://dx.doi.org/10.3389/fbioe.2021.796361 Text en Copyright © 2022 Lin, Zhao, Xu, Zhou, Wang, Chen and Mei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Lin, Sen Zhao, Hao-sen Xu, Chang Zhou, Zi-peng Wang, Da-hao Chen, Shu-rui Mei, Xi-fan Bioengineered Zinc Oxide Nanoparticle-Loaded Hydrogel for Combinative Treatment of Spinal Cord Transection |
title | Bioengineered Zinc Oxide Nanoparticle-Loaded Hydrogel for Combinative Treatment of Spinal Cord Transection |
title_full | Bioengineered Zinc Oxide Nanoparticle-Loaded Hydrogel for Combinative Treatment of Spinal Cord Transection |
title_fullStr | Bioengineered Zinc Oxide Nanoparticle-Loaded Hydrogel for Combinative Treatment of Spinal Cord Transection |
title_full_unstemmed | Bioengineered Zinc Oxide Nanoparticle-Loaded Hydrogel for Combinative Treatment of Spinal Cord Transection |
title_short | Bioengineered Zinc Oxide Nanoparticle-Loaded Hydrogel for Combinative Treatment of Spinal Cord Transection |
title_sort | bioengineered zinc oxide nanoparticle-loaded hydrogel for combinative treatment of spinal cord transection |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793849/ https://www.ncbi.nlm.nih.gov/pubmed/35096792 http://dx.doi.org/10.3389/fbioe.2021.796361 |
work_keys_str_mv | AT linsen bioengineeredzincoxidenanoparticleloadedhydrogelforcombinativetreatmentofspinalcordtransection AT zhaohaosen bioengineeredzincoxidenanoparticleloadedhydrogelforcombinativetreatmentofspinalcordtransection AT xuchang bioengineeredzincoxidenanoparticleloadedhydrogelforcombinativetreatmentofspinalcordtransection AT zhouzipeng bioengineeredzincoxidenanoparticleloadedhydrogelforcombinativetreatmentofspinalcordtransection AT wangdahao bioengineeredzincoxidenanoparticleloadedhydrogelforcombinativetreatmentofspinalcordtransection AT chenshurui bioengineeredzincoxidenanoparticleloadedhydrogelforcombinativetreatmentofspinalcordtransection AT meixifan bioengineeredzincoxidenanoparticleloadedhydrogelforcombinativetreatmentofspinalcordtransection |