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克服药物递送中的内体捕获。

Overcoming Endosomal Entrapment in Drug Delivery.

机构信息

Department of Chemistry and Biochemistry , The Ohio State University , 484 West 12th Avenue , Columbus , Ohio 43210 , United States.

出版信息

Bioconjug Chem. 2019 Feb 20;30(2):273-283. doi: 10.1021/acs.bioconjchem.8b00778. Epub 2018 Dec 19.

DOI:10.1021/acs.bioconjchem.8b00778
PMID:30525488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6501178/
Abstract

Intracellular delivery of biological agents such as peptides, proteins, and nucleic acids generally rely on the endocytic pathway as the major uptake mechanism, resulting in their entrapment inside the endosome and lysosome. The recent discovery of cell-penetrating molecules of exceptionally high endosomal escape and cytosolic delivery efficiencies and elucidation of their mechanism of action represent major breakthroughs in this field. In this Topical Review, we provide an overview of the recent progress in understanding and enhancing the endosomal escape process and the new opportunities opened up by these recent findings.

摘要

细胞内递呈生物制剂(如肽、蛋白质和核酸)通常依赖内吞途径作为主要的摄取机制,导致它们被捕获在内体和溶酶体中。最近发现了具有极高的内体逃逸和细胞质递呈效率的细胞穿透分子,并阐明了它们的作用机制,这是该领域的重大突破。在这篇专题综述中,我们概述了对内体逃逸过程的理解和增强的最新进展,以及这些新发现带来的新机遇。

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J Mater Chem B. 2017 Jan 7;5(1):74-84. doi: 10.1039/c6tb02862d. Epub 2016 Nov 30.
2
The great escape: how cationic polyplexes overcome the endosomal barrier.大逃亡:阳离子多聚体如何克服内体屏障。
J Mater Chem B. 2018 Nov 21;6(43):6904-6918. doi: 10.1039/c8tb00967h. Epub 2018 Sep 26.
3
Non-Peptidic Cell-Penetrating Motifs for Mitochondrion-Specific Cargo Delivery.
ACS Omega. 2025 Jul 25;10(30):32744-32753. doi: 10.1021/acsomega.4c11519. eCollection 2025 Aug 5.
4
A modular polymer platform for efficient mRNA delivery in cancer immunotherapy.一种用于癌症免疫治疗中高效递送信使核糖核酸的模块化聚合物平台。
Nanoscale Horiz. 2025 Aug 7. doi: 10.1039/d5nh00299k.
5
Harnessing Nanomaterials for Precision Intracellular Sensing.利用纳米材料进行精准细胞内传感。
JACS Au. 2025 Jul 10;5(7):2939-2952. doi: 10.1021/jacsau.5c00420. eCollection 2025 Jul 28.
6
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Pharmaceutics. 2025 Jul 12;17(7):903. doi: 10.3390/pharmaceutics17070903.
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Discov Nano. 2025 Jul 26;20(1):119. doi: 10.1186/s11671-025-04316-5.
8
Riding the wave of innovation: nanotechnology in nucleic acid-based cancer therapy.乘创新之浪:基于核酸的癌症治疗中的纳米技术
3 Biotech. 2025 Jul;15(7):226. doi: 10.1007/s13205-025-04397-0. Epub 2025 Jun 27.
9
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