Suppr超能文献

利用静电相互作用促进聚(酰胺)胺(PAMAM)树枝状大分子的F-18放射性标记。

Utilizing electrostatic interactions to facilitate F-18 radiolabeling of poly(amido)amine (PAMAM) dendrimers.

作者信息

Zhou Dong, Kim Sung Hoon, Carroll Vincent M, Dence Carmen S, Katzenellenbogen John A

机构信息

Washington University Medical School, Mallinckrodt Institute of Radiology, Saint Louis, MO 63110, USA.

出版信息

Org Biomol Chem. 2014 Nov 21;12(43):8696-701. doi: 10.1039/c4ob01616e.

Abstract

The development of methods for the facile conjugation and radiolabeling of poly(amido)amine (PAMAM) dendrimers would be of great benefit in evaluating biomedical applications of these intriguing molecularly defined polymers. Two anionic N-hydroxysuccinimide (NHS) esters (7 and 10) were developed and radiolabeled with fluorine-18 using Cu(I)-catalyzed click reactions. The radiolabeling of a primary amine-terminated PAMAM generation-6 (G6) dendrimer with [(18)F]7 or [(18)F]10 was complete in water or methanol within 5 min at room temperature. This highly efficient conjugation reaction benefits from a high, localized concentration of these NHS esters on the surface of PAMAM dendrimers, due to the electrostatic attraction between the anionic NHS esters and the positively-charged PAMAM dendrimers. The large medium effect (pH, salt, solvent) observed for these conjugation reactions is consistent with this mechanism. This novel strategy of utilizing electrostatic interactions provides a novel, facile, and efficient method for the conjugation and radiolabeling of PAMAM dendrimers that also has potential for radiolabeling other appropriate nanoparticles.

摘要

开发用于聚(酰胺)胺(PAMAM)树枝状大分子的简便共轭和放射性标记方法,对于评估这些有趣的分子定义聚合物的生物医学应用将大有裨益。开发了两种阴离子N-羟基琥珀酰亚胺(NHS)酯(7和10),并使用铜(I)催化的点击反应将其用氟-18进行放射性标记。在室温下,用[(18)F]7或[(18)F]10对伯胺封端的第6代(G6)PAMAM树枝状大分子进行放射性标记,在水或甲醇中5分钟内即可完成。这种高效的共轭反应得益于这些NHS酯在PAMAM树枝状大分子表面的高局部浓度,这是由于阴离子NHS酯与带正电荷的PAMAM树枝状大分子之间的静电吸引。这些共轭反应中观察到的较大介质效应(pH、盐、溶剂)与该机制一致。这种利用静电相互作用的新策略为PAMAM树枝状大分子的共轭和放射性标记提供了一种新颖、简便且高效的方法,该方法也具有对其他合适的纳米颗粒进行放射性标记的潜力。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验