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Nanomaterials for mRNA‐based therapeutics: Challenges and opportunities

Messenger RNA (mRNA) holds great potential in developing immunotherapy, protein replacement, and genome editing. In general, mRNA does not have the risk of being incorporated into the host genome and does not need to enter the nucleus for transfection, and it can be expressed even in nondividing cel...

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Autores principales: Li, De‐feng, Liu, Qi‐song, Yang, Mei‐feng, Xu, Hao‐ming, Zhu, Min‐zheng, Zhang, Yuan, Xu, Jing, Tian, Cheng‐mei, Yao, Jun, Wang, Li‐sheng, Liang, Yu‐jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189457/
https://www.ncbi.nlm.nih.gov/pubmed/37206219
http://dx.doi.org/10.1002/btm2.10492
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author Li, De‐feng
Liu, Qi‐song
Yang, Mei‐feng
Xu, Hao‐ming
Zhu, Min‐zheng
Zhang, Yuan
Xu, Jing
Tian, Cheng‐mei
Yao, Jun
Wang, Li‐sheng
Liang, Yu‐jie
author_facet Li, De‐feng
Liu, Qi‐song
Yang, Mei‐feng
Xu, Hao‐ming
Zhu, Min‐zheng
Zhang, Yuan
Xu, Jing
Tian, Cheng‐mei
Yao, Jun
Wang, Li‐sheng
Liang, Yu‐jie
author_sort Li, De‐feng
collection PubMed
description Messenger RNA (mRNA) holds great potential in developing immunotherapy, protein replacement, and genome editing. In general, mRNA does not have the risk of being incorporated into the host genome and does not need to enter the nucleus for transfection, and it can be expressed even in nondividing cells. Therefore, mRNA‐based therapeutics provide a promising strategy for clinical treatment. However, the efficient and safe delivery of mRNA remains a crucial constraint for the clinical application of mRNA therapeutics. Although the stability and tolerability of mRNA can be enhanced by directly retouching the mRNA structure, there is still an urgent need to improve the delivery of mRNA. Recently, significant progress has been made in nanobiotechnology, providing tools for developing mRNA nanocarriers. Nano‐drug delivery system is directly used for loading, protecting, and releasing mRNA in the biological microenvironment and can be used to stimulate the translation of mRNA to develop effective intervention strategies. In the present review, we summarized the concept of emerging nanomaterials for mRNA delivery and the latest progress in enhancing the function of mRNA, primarily focusing on the role of exosomes in mRNA delivery. Moreover, we outlined its clinical applications so far. Finally, the key obstacles of mRNA nanocarriers are emphasized, and promising strategies to overcome these obstacles are proposed. Collectively, nano‐design materials exert functions for specific mRNA applications, provide new perception for next‐generation nanomaterials, and thus revolution of mRNA technology.
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spelling pubmed-101894572023-05-18 Nanomaterials for mRNA‐based therapeutics: Challenges and opportunities Li, De‐feng Liu, Qi‐song Yang, Mei‐feng Xu, Hao‐ming Zhu, Min‐zheng Zhang, Yuan Xu, Jing Tian, Cheng‐mei Yao, Jun Wang, Li‐sheng Liang, Yu‐jie Bioeng Transl Med Review Articles Messenger RNA (mRNA) holds great potential in developing immunotherapy, protein replacement, and genome editing. In general, mRNA does not have the risk of being incorporated into the host genome and does not need to enter the nucleus for transfection, and it can be expressed even in nondividing cells. Therefore, mRNA‐based therapeutics provide a promising strategy for clinical treatment. However, the efficient and safe delivery of mRNA remains a crucial constraint for the clinical application of mRNA therapeutics. Although the stability and tolerability of mRNA can be enhanced by directly retouching the mRNA structure, there is still an urgent need to improve the delivery of mRNA. Recently, significant progress has been made in nanobiotechnology, providing tools for developing mRNA nanocarriers. Nano‐drug delivery system is directly used for loading, protecting, and releasing mRNA in the biological microenvironment and can be used to stimulate the translation of mRNA to develop effective intervention strategies. In the present review, we summarized the concept of emerging nanomaterials for mRNA delivery and the latest progress in enhancing the function of mRNA, primarily focusing on the role of exosomes in mRNA delivery. Moreover, we outlined its clinical applications so far. Finally, the key obstacles of mRNA nanocarriers are emphasized, and promising strategies to overcome these obstacles are proposed. Collectively, nano‐design materials exert functions for specific mRNA applications, provide new perception for next‐generation nanomaterials, and thus revolution of mRNA technology. John Wiley & Sons, Inc. 2023-01-29 /pmc/articles/PMC10189457/ /pubmed/37206219 http://dx.doi.org/10.1002/btm2.10492 Text en © 2023 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Articles
Li, De‐feng
Liu, Qi‐song
Yang, Mei‐feng
Xu, Hao‐ming
Zhu, Min‐zheng
Zhang, Yuan
Xu, Jing
Tian, Cheng‐mei
Yao, Jun
Wang, Li‐sheng
Liang, Yu‐jie
Nanomaterials for mRNA‐based therapeutics: Challenges and opportunities
title Nanomaterials for mRNA‐based therapeutics: Challenges and opportunities
title_full Nanomaterials for mRNA‐based therapeutics: Challenges and opportunities
title_fullStr Nanomaterials for mRNA‐based therapeutics: Challenges and opportunities
title_full_unstemmed Nanomaterials for mRNA‐based therapeutics: Challenges and opportunities
title_short Nanomaterials for mRNA‐based therapeutics: Challenges and opportunities
title_sort nanomaterials for mrna‐based therapeutics: challenges and opportunities
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189457/
https://www.ncbi.nlm.nih.gov/pubmed/37206219
http://dx.doi.org/10.1002/btm2.10492
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