Suppr超能文献

聚二硫键钆(III)螯合物作为可生物降解的大分子磁共振成像造影剂。

Polydisulfide Gd(III) chelates as biodegradable macromolecular magnetic resonance imaging contrast agents.

作者信息

Lu Zheng-Rong, Mohs Aaron M, Zong Yuda, Feng Yi

机构信息

Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84108, USA.

出版信息

Int J Nanomedicine. 2006;1(1):31-40. doi: 10.2147/nano.2006.1.1.31.

Abstract

Macromolecular gadolinium (Gd)(III) complexes have a prolonged blood circulation time and can preferentially accumulate in solid tumors, depending on the tumor blood vessel hyperpermeability, resulting in superior contrast enhancement in magnetic resonance (MR) cardiovascular imaging and cancer imaging as shown in animal models. Unfortunately, safety concerns related to these agents' slow elimination from the body impede their clinical development. Polydisulfide Gd(III) complexes have been designed and developed as biodegradable macromolecular magnetic resonance imaging (MRI) contrast agents to facilitate the clearance of Gd(III) complexes from the body after MRI examinations. These novel agents can act as macromolecular contrast agents for in vivo imaging and excrete rapidly as low-molecular-weight agents. The rationale and recent development of the novel biodegradable contrast agents are reviewed here. Polydisulfide Gd(III) complexes have relatively long blood circulation time and gradually degrade into small Gd(III) complexes, which are rapidly excreted via renal filtration. These agents result in effective and prolonged in vivo contrast enhancement in the blood pool and tumor tissue in animal models, yet demonstrate minimal Gd(III) tissue retention as the clinically used low-molecular-weight agents. Structural modification of the agents can readily alter the contrast-enhancement kinetics. Polydisulfide Gd(III) complexes are promising for further clinical development as safe, effective, biodegradable macromolecular MRI contrast agents for cardiovascular and cancer imaging, and for evaluation of therapeutic response.

摘要

大分子钆(Gd)(III)配合物具有较长的血液循环时间,并且根据肿瘤血管的高渗透性,能够优先在实体瘤中蓄积,这使得其在动物模型的磁共振(MR)心血管成像和癌症成像中具有卓越的对比增强效果。不幸的是,与这些造影剂从体内缓慢清除相关的安全性问题阻碍了它们的临床开发。聚二硫化合物Gd(III)配合物已被设计和开发为可生物降解的大分子磁共振成像(MRI)造影剂,以便在MRI检查后促进Gd(III)配合物从体内清除。这些新型造影剂可作为体内成像的大分子造影剂,并以低分子量造影剂的形式迅速排出。本文综述了新型可生物降解造影剂的原理及近期进展。聚二硫化合物Gd(III)配合物具有相对较长的血液循环时间,并逐渐降解为小的Gd(III)配合物,这些小配合物通过肾脏滤过迅速排出。在动物模型中,这些造影剂在血池和肿瘤组织中可产生有效且持久的体内对比增强效果,但与临床使用的低分子量造影剂相比,其在组织中的钆(III)潴留量极少。对造影剂进行结构修饰可轻易改变对比增强动力学。聚二硫化合物Gd(III)配合物作为安全、有效、可生物降解的大分子MRI造影剂用于心血管和癌症成像以及治疗反应评估,具有进一步临床开发的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a998/2426761/2f9a30c5bafc/nano0101-31-01.jpg

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