Insights into the formulation of lipid nanoparticles for the optimization of mRNA therapeutics.

Xiangyu Jiao, Xi He, Shugang Qin, Xiaoling Yin, Tingting Song, Xing Duan, Haixing Shi, Shanhui Jiang, Yupei Zhang, Xiangrong Song
{"title":"Insights into the formulation of lipid nanoparticles for the optimization of mRNA therapeutics.","authors":"Xiangyu Jiao, Xi He, Shugang Qin, Xiaoling Yin, Tingting Song, Xing Duan, Haixing Shi, Shanhui Jiang, Yupei Zhang, Xiangrong Song","doi":"10.1002/wnan.1992","DOIUrl":null,"url":null,"abstract":"<p><p>mRNA-based therapeutics increasingly demonstrate significant potential in treating various diseases, including infectious diseases, cancers, and genetic disorders. Effective delivery systems are crucial for advancing mRNA therapeutics. Lipid nanoparticles (LNPs) serve as an excellent carrier, widely validated for their safety and tolerability in commercially available mRNA vaccines. Standard LNPs typically consist of four components: ionizable lipids (ILs), helper lipids, cholesterol, and polyethylene glycol-lipids (PEG-lipids), with the structural design of ILs gradually becoming a focal point of research interest. The chemical structures and formulations of the other components also significantly affect the delivery efficiency, targeting specificity, and stability of LNPs. The complex formulations of LNPs may hinder the clinical transformation of mRNA therapeutics and have raised widespread concerns about their safety. This review aims to summarize the progress of LNPs-based mRNA therapeutics in clinical trials, focusing on adverse effects that occurred during these trials. It also discusses representative innovations in LNP components, highlighting challenges and potential ways in this research field. We firmly believe this review will promote further improvements and designs of LNP compositions to optimize mRNA therapeutics. This article is categorized under: Nanotechnology Approaches to Biology > Nanoscale Systems in Biology Biology-Inspired Nanomaterials > Lipid-Based Structures.</p>","PeriodicalId":94267,"journal":{"name":"Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology","volume":"16 5","pages":"e1992"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/wnan.1992","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

mRNA-based therapeutics increasingly demonstrate significant potential in treating various diseases, including infectious diseases, cancers, and genetic disorders. Effective delivery systems are crucial for advancing mRNA therapeutics. Lipid nanoparticles (LNPs) serve as an excellent carrier, widely validated for their safety and tolerability in commercially available mRNA vaccines. Standard LNPs typically consist of four components: ionizable lipids (ILs), helper lipids, cholesterol, and polyethylene glycol-lipids (PEG-lipids), with the structural design of ILs gradually becoming a focal point of research interest. The chemical structures and formulations of the other components also significantly affect the delivery efficiency, targeting specificity, and stability of LNPs. The complex formulations of LNPs may hinder the clinical transformation of mRNA therapeutics and have raised widespread concerns about their safety. This review aims to summarize the progress of LNPs-based mRNA therapeutics in clinical trials, focusing on adverse effects that occurred during these trials. It also discusses representative innovations in LNP components, highlighting challenges and potential ways in this research field. We firmly believe this review will promote further improvements and designs of LNP compositions to optimize mRNA therapeutics. This article is categorized under: Nanotechnology Approaches to Biology > Nanoscale Systems in Biology Biology-Inspired Nanomaterials > Lipid-Based Structures.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
脂质纳米颗粒配方对优化 mRNA 治疗的启示。
基于 mRNA 的疗法在治疗各种疾病(包括传染病、癌症和遗传性疾病)方面日益显示出巨大的潜力。有效的递送系统对于推进 mRNA 疗法至关重要。脂质纳米颗粒(LNPs)是一种出色的载体,其安全性和耐受性在市售 mRNA 疫苗中得到了广泛验证。标准 LNPs 通常由四种成分组成:可电离脂质(ILs)、辅助脂质、胆固醇和聚乙二醇脂质(PEG-lipids)。其他成分的化学结构和配方也会对 LNPs 的递送效率、靶向特异性和稳定性产生重要影响。LNPs 的复杂配方可能会阻碍 mRNA 疗法的临床转化,并引起人们对其安全性的广泛关注。本综述旨在总结基于 LNPs 的 mRNA 疗法在临床试验中的进展,重点关注这些试验中出现的不良反应。它还讨论了 LNP 成分的代表性创新,强调了该研究领域的挑战和潜在途径。我们坚信,这篇综述将促进 LNP 成分的进一步改进和设计,从而优化 mRNA 疗法。本文归类于生物纳米技术 > 生物学中的纳米尺度系统 生物学启发的纳米材料 > 脂基结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
17.60
自引率
0.00%
发文量
0
期刊最新文献
Iron-Based Nanomaterials for Modulating Tumor Microenvironment. Polymers for mRNA Delivery. Pulmonary Delivery of Nonviral Nucleic Acid-Based Vaccines With Spotlight on Gold Nanoparticles. Recent Advances in Wearable Sweat Sensor Development. Biomimetic Nanomaterials Based on Peptide In Situ Self-Assembly for Immunotherapy Applications.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1