Suppr超能文献

探讨金属配合物的细胞积累。

Exploring the cellular accumulation of metal complexes.

机构信息

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

出版信息

Dalton Trans. 2010 Feb 7;39(5):1159-70. doi: 10.1039/b922209j. Epub 2009 Dec 23.

Abstract

Transition metal complexes offer great potential as diagnostic and therapeutic agents, and a growing number of biological applications have been explored. To be effective, these complexes must reach their intended target inside the cell. Here we review the cellular accumulation of metal complexes, including their uptake, localization, and efflux. Metal complexes are taken up inside cells through various mechanisms, including passive diffusion and entry through organic and metal transporters. Emphasis is placed on the methods used to examine cellular accumulation, to identify the mechanism(s) of uptake, and to monitor possible efflux. Conjugation strategies that have been employed to improve the cellular uptake characteristics of metal complexes are also described.

摘要

过渡金属配合物作为诊断和治疗试剂具有巨大的潜力,越来越多的生物应用已经得到了探索。为了有效,这些配合物必须到达细胞内的预期靶点。在这里,我们回顾了金属配合物的细胞积累,包括它们的摄取、定位和外排。金属配合物通过多种机制被细胞摄取,包括被动扩散和通过有机和金属转运体进入。重点介绍了用于检查细胞积累、确定摄取机制以及监测可能的外排的方法。还描述了为了提高金属配合物的细胞摄取特性而采用的偶联策略。

相似文献

1
Exploring the cellular accumulation of metal complexes.探讨金属配合物的细胞积累。
Dalton Trans. 2010 Feb 7;39(5):1159-70. doi: 10.1039/b922209j. Epub 2009 Dec 23.

引用本文的文献

本文引用的文献

7
Mechanisms of endocytosis.内吞作用的机制。
Annu Rev Biochem. 2009;78:857-902. doi: 10.1146/annurev.biochem.78.081307.110540.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验