局部给药纳米颗粒增强表面渗透性和滞留效果。

IF 3.9 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Yiyang Chen, Zhenghong Liu, Bin Zheng, Chenkai Wang, Xintao Hua, Pu Zhang, Dahong Zhang
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引用次数: 0

摘要

局部给药为纳米颗粒(NPs)提供了到达肿瘤表面的直接途径,比静脉给药具有更局部和直接的治疗效果,同时保证了更高的生物安全性。通过利用肿瘤独特的表面结构,这些颗粒在腔内扩散,然后靶向转运到肿瘤组织中,这被称为增强表面渗透性和保留(ESPR)效应。重要的是,通过局部给药,腔内纳米颗粒的ESPR效应不依赖于肿瘤靶向配体-受体的相互作用。本文综述了局部给药治疗的临床现状,阐述了ESPR作用的机制,并对如何调节ESPR作用进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The enhanced surface permeability and retention effect of topically administrated nanoparticles.

Topical administration provides direct way for nanoparticles (NPs) to reach the tumour surface, inducing a more localised and direct therapeutic effect than what intravenous therapy can do and meanwhile guaranteeing higher biosafety. By leveraging the unique surface structure of tumours, these particles undergo intracavity diffusion and afterwards targeted transport into the tumour tissue, which is termed as the enhanced surface permeability and retention (ESPR) effect. Importantly, the ESPR effect of intracavity nanoparticles via topical administration does not rely on tumour-targeted ligand-receptor interactions. In this review, the current clinical status of topical administration-based therapy is updated, the mechanism of the ESPR effect is elucidated and how to modulate the ESPR effect is summarised.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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