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Can Manganese Dioxide Microspheres be Used as Intermediaries to Alleviate Intervertebral Disc Degeneration With Strengthening Drugs?

Degenerative disc disease (DDD) is a pathological condition associated with intervertebral discs (IVDs) that causes chronic back pain. IVD degeneration has become a significant issue in contemporary society. To date, numerous biological therapies have been applied to alleviate the progression of DDD...

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Autores principales: Zhang, Wentao, Yang, Ming, Sun, Tianze, Zhang, Jing, Zhao, Yantao, Li, Jingmin, Li, Zhonghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011040/
https://www.ncbi.nlm.nih.gov/pubmed/35433668
http://dx.doi.org/10.3389/fbioe.2022.866290
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author Zhang, Wentao
Yang, Ming
Sun, Tianze
Zhang, Jing
Zhao, Yantao
Li, Jingmin
Li, Zhonghai
author_facet Zhang, Wentao
Yang, Ming
Sun, Tianze
Zhang, Jing
Zhao, Yantao
Li, Jingmin
Li, Zhonghai
author_sort Zhang, Wentao
collection PubMed
description Degenerative disc disease (DDD) is a pathological condition associated with intervertebral discs (IVDs) that causes chronic back pain. IVD degeneration has become a significant issue in contemporary society. To date, numerous biological therapies have been applied to alleviate the progression of DDD, among which therapeutic protein injection is the most direct and convenient. However, there are some limitations to applying direct protein injection therapy, the most significant being that the efficacy of this method has a short duration, which is a major factor in its effectiveness and the resulting patient satisfaction. How do we solve this problem? Or how can the effectiveness of the treatment be enhanced? It has been proved that manganese dioxide (MnO(2)) microspheres, widely used in environmental science, not only regulate the expression of cell genes and cytokines in the microenvironment, but also have the ability to release drugs slowly. We propose that direct injection of protein encapsulated in hollow MnO(2) (h-MnO(2)) microspheres could solve the problem of rapid drug release. In addition, the use of a MnO(2) and protein injection in the treatment of DDD may have a synergistic effect, which would be highly significant for the degradation of pro-inflammatory factors in the DDD microenvironment. Therefore, the combination of MnO(2) and protein may provide a new therapeutic approach to alleviate the progression of DDD.
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spelling pubmed-90110402022-04-16 Can Manganese Dioxide Microspheres be Used as Intermediaries to Alleviate Intervertebral Disc Degeneration With Strengthening Drugs? Zhang, Wentao Yang, Ming Sun, Tianze Zhang, Jing Zhao, Yantao Li, Jingmin Li, Zhonghai Front Bioeng Biotechnol Bioengineering and Biotechnology Degenerative disc disease (DDD) is a pathological condition associated with intervertebral discs (IVDs) that causes chronic back pain. IVD degeneration has become a significant issue in contemporary society. To date, numerous biological therapies have been applied to alleviate the progression of DDD, among which therapeutic protein injection is the most direct and convenient. However, there are some limitations to applying direct protein injection therapy, the most significant being that the efficacy of this method has a short duration, which is a major factor in its effectiveness and the resulting patient satisfaction. How do we solve this problem? Or how can the effectiveness of the treatment be enhanced? It has been proved that manganese dioxide (MnO(2)) microspheres, widely used in environmental science, not only regulate the expression of cell genes and cytokines in the microenvironment, but also have the ability to release drugs slowly. We propose that direct injection of protein encapsulated in hollow MnO(2) (h-MnO(2)) microspheres could solve the problem of rapid drug release. In addition, the use of a MnO(2) and protein injection in the treatment of DDD may have a synergistic effect, which would be highly significant for the degradation of pro-inflammatory factors in the DDD microenvironment. Therefore, the combination of MnO(2) and protein may provide a new therapeutic approach to alleviate the progression of DDD. Frontiers Media S.A. 2022-04-01 /pmc/articles/PMC9011040/ /pubmed/35433668 http://dx.doi.org/10.3389/fbioe.2022.866290 Text en Copyright © 2022 Zhang, Yang, Sun, Zhang, Zhao, Li and Li. 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
Zhang, Wentao
Yang, Ming
Sun, Tianze
Zhang, Jing
Zhao, Yantao
Li, Jingmin
Li, Zhonghai
Can Manganese Dioxide Microspheres be Used as Intermediaries to Alleviate Intervertebral Disc Degeneration With Strengthening Drugs?
title Can Manganese Dioxide Microspheres be Used as Intermediaries to Alleviate Intervertebral Disc Degeneration With Strengthening Drugs?
title_full Can Manganese Dioxide Microspheres be Used as Intermediaries to Alleviate Intervertebral Disc Degeneration With Strengthening Drugs?
title_fullStr Can Manganese Dioxide Microspheres be Used as Intermediaries to Alleviate Intervertebral Disc Degeneration With Strengthening Drugs?
title_full_unstemmed Can Manganese Dioxide Microspheres be Used as Intermediaries to Alleviate Intervertebral Disc Degeneration With Strengthening Drugs?
title_short Can Manganese Dioxide Microspheres be Used as Intermediaries to Alleviate Intervertebral Disc Degeneration With Strengthening Drugs?
title_sort can manganese dioxide microspheres be used as intermediaries to alleviate intervertebral disc degeneration with strengthening drugs?
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011040/
https://www.ncbi.nlm.nih.gov/pubmed/35433668
http://dx.doi.org/10.3389/fbioe.2022.866290
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