Harnessing exosomes for targeted therapy: strategy and application.

Biomaterials Translational Pub Date : 2024-03-28 eCollection Date: 2024-01-01 DOI:10.12336/biomatertransl.2024.01.005
Xiaoxiang Ren, Ruixue Xu, Chenjie Xu, Jiacan Su
{"title":"Harnessing exosomes for targeted therapy: strategy and application.","authors":"Xiaoxiang Ren, Ruixue Xu, Chenjie Xu, Jiacan Su","doi":"10.12336/biomatertransl.2024.01.005","DOIUrl":null,"url":null,"abstract":"<p><p>Exosomes, nanoscopic extracellular vesicles produced by cells, are pivotal in mediating intracellular communication by transporting nucleic acids, proteins, lipids, and other bioactive molecules, thereby influencing physiological and pathological states. Their endogenous origin and inherent diversity confer distinct advantages over synthetic vehicles like liposomes and nanoparticles in diagnostic and therapeutic applications. Despite their potential, the clinical utility of exosomes is hampered by challenges such as limited storage stability, yield, purity, and targeting efficiency. This review focuses on exosomes as targeted therapeutic agents, examining their biogenesis, classification, isolation, and characterisation, while also addressing the current limitations in yield, purity, and targeting. We delve into the literature to propose optimisation strategies that can enhance their therapeutic efficacy and accelerate the translation of exosome-based therapies into clinical practice.</p>","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 1","pages":"46-58"},"PeriodicalIF":0.0000,"publicationDate":"2024-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11362351/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomaterials Translational","FirstCategoryId":"1087","ListUrlMain":"https://doi.org/10.12336/biomatertransl.2024.01.005","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Exosomes, nanoscopic extracellular vesicles produced by cells, are pivotal in mediating intracellular communication by transporting nucleic acids, proteins, lipids, and other bioactive molecules, thereby influencing physiological and pathological states. Their endogenous origin and inherent diversity confer distinct advantages over synthetic vehicles like liposomes and nanoparticles in diagnostic and therapeutic applications. Despite their potential, the clinical utility of exosomes is hampered by challenges such as limited storage stability, yield, purity, and targeting efficiency. This review focuses on exosomes as targeted therapeutic agents, examining their biogenesis, classification, isolation, and characterisation, while also addressing the current limitations in yield, purity, and targeting. We delve into the literature to propose optimisation strategies that can enhance their therapeutic efficacy and accelerate the translation of exosome-based therapies into clinical practice.

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
利用外泌体进行靶向治疗:策略与应用。
外泌体是细胞产生的纳米级细胞外囊泡,通过运输核酸、蛋白质、脂质和其他生物活性分子,在介导细胞内交流方面发挥着关键作用,从而影响生理和病理状态。在诊断和治疗应用中,与脂质体和纳米颗粒等合成载体相比,小体的内源性来源和固有多样性具有明显优势。尽管外泌体潜力巨大,但其临床应用却受到存储稳定性、产量、纯度和靶向效率等方面挑战的制约。本综述侧重于外泌体作为靶向治疗药物,研究其生物发生、分类、分离和表征,同时探讨目前在产量、纯度和靶向性方面的局限性。我们深入研究文献,提出优化策略,以提高外泌体的疗效,加快将基于外泌体的疗法转化为临床实践。
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
6.70
自引率
0.00%
发文量
9
期刊最新文献
"Yin-Yang philosophy" for the design of anticancer drug delivery nanoparticles. Abalone shell-derived Mg-doped mesoporous hydroxyapatite microsphere drug delivery system loaded with icariin for inducing apoptosis of osteosarcoma cells. Advanced nanoparticles in osteoarthritis treatment. Artificial intelligence-enabled studies on organoid and organoid extracellular vesicles. Corrigendum: Enhanced angiogenesis in porous poly(ε-caprolactone) scaffolds fortified with methacrylated hyaluronic acid hydrogel after subcutaneous transplantation.
×
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