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多价药物递送-物极必反?

Multivalency in Drug Delivery-When Is It Too Much of a Good Thing?

机构信息

School of Chemistry, the Australian Centre for Nanomedicine and the ARC Centre of Excellence in Convergent Bio-Nano Science and Technology , The University of New South Wales , Sydney , New South Wales 2052 , Australia.

出版信息

Bioconjug Chem. 2019 Mar 20;30(3):503-514. doi: 10.1021/acs.bioconjchem.8b00804. Epub 2019 Feb 22.

Abstract

Multivalency plays a large role in many biological and synthetic systems. The past 20 years of research have seen an explosion in the study of multivalent drug delivery systems based on scaffolds such as dendrimers, polymers, and other nanoparticles. The results from these studies suggest that when it comes to the number of ligands, sometimes, to quote Shakespeare, "too much of a good thing" is an apt description. Recent theoretical studies on multivalency indicate that the field may have had a misplaced emphasis on maximizing binding strength where in fact it is the selectivity of multivalent drug delivery systems that is the key to success. This Topical Review will summarize these theoretical developments. We will then illustrate how these developments can be used to rationalize the immunoresponses and drug uptake mechanisms for multivalent systems and show the path forward toward the design of better multivalent drug delivery systems.

摘要

多价性在许多生物和合成系统中起着重要作用。在过去的 20 年中,基于树状聚合物、聚合物和其他纳米粒子等支架的多价药物传递系统的研究呈爆炸式增长。这些研究的结果表明,就配体的数量而言,有时,用莎士比亚的话说,“太多的好事”是一个恰当的描述。最近关于多价性的理论研究表明,该领域可能过分强调了最大化结合强度,而实际上,多价药物传递系统的选择性是成功的关键。本专题评论将总结这些理论进展。然后,我们将说明如何利用这些进展来合理化多价系统的免疫反应和药物摄取机制,并展示设计更好的多价药物传递系统的前进道路。

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