跨细胞药物传递的直接转移方法。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2023-12-01 Epub Date: 2023-11-30 DOI:10.1080/10717544.2023.2288799
Yi-Fan Wang, Ze-Fan Shen, Fang-Yue Xiang, Heng Wang, Pu Zhang, Qi Zhang
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引用次数: 0

摘要

近年来引起越来越多关注的一种有前途的药物给药范例是纳米颗粒的直接转移(DT),用于跨细胞药物递送。DT要求细胞间直接接触,促进相邻细胞间的单向和双向物质交换。因此,DT可以使药物快速深入渗透到目标组织中。这篇综述讨论了直接转移的概念,它可以分为以下三种不同的模式:膜接触直接转移,间隙连接介导的直接转移(GJ-DT)和隧道纳米管介导的直接转移(tnt - dt)。此外,还总结了每种直接转移方式的细胞间结构及其各自的优缺点。本文还讨论了可激活DT的药物或药物传递系统的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The direct transfer approach for transcellular drug delivery.

A promising paradigm for drug administration that has garnered increasing attention in recent years is the direct transfer (DT) of nanoparticles for transcellular drug delivery. DT requires direct cell-cell contact and facilitates unidirectional and bidirectional matter exchange between neighboring cells. Consequently, DT enables fast and deep penetration of drugs into the targeted tissues. This comprehensive review discusses the direct transfer concept, which can be delineated into the following three distinct modalities: membrane contact-direct transfer, gap junction-mediated direct transfer (GJ-DT), and tunneling nanotubes-mediated direct transfer (TNTs-DT). Further, the intercellular structures for each modality of direct transfer and their respective merits and demerits are summarized. The review also discusses the recent progress on the drugs or drug delivery systems that could activate DT.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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