Radioimmune & Inorganic Chemistry Section, Radiation Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
Bioorg Med Chem. 2010 Aug 15;18(16):5925-31. doi: 10.1016/j.bmc.2010.06.086. Epub 2010 Jul 8.
In this report we directly compare the in vivo and in vitro MRI properties of gadolinium-dendrimer conjugates of derivatized acyclic diethylenetriamine-N,N',N',N'',N''-pentaacetic acid (1B4M-DTPA) and macrocyclic 1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic acid (C-DOTA). The metal-ligand chelates were pre-formed in alcohol prior to conjugation to the generation 4 PAMAM dendrimer (G4D), and the dendrimer-based agents were purified by Sephadex(R) G-25 column. The analysis and SE-HPLC data indicated chelate to dendrimer ratios of 30:1 and 28:1, respectively. Molar relaxivity measured at pH 7.4, 22 degrees C, and 3T are comparable (29.5 vs 26.9 mM(-1)s(-1)), and both conjugates are equally viable as MRI contrast agents based on the images obtained. The macrocyclic agent however exhibits a faster rate of clearance in vivo (t(1/2)=16 vs 29 min). Our conclusion is that the macrocyclic-based agent is the more suitable agent for in vivo use for these reasons combined with kinetic inertness associated with the Gd(III) DOTA complex stability properties.
在本报告中,我们直接比较了衍生的非循环二亚乙基三胺-N,N',N',N'',N''-五乙酸(1B4M-DTPA)和大环 1,4,7,10-四氮杂环十二烷-N,N',N'',N'''-四乙酸(C-DOTA)的钆树枝状大分子缀合物的体内和体外 MRI 性质。金属配体螯合物在与第 4 代聚酰胺胺(G4D)缀合之前在醇中预先形成,并通过葡聚糖(R)G-25 柱对基于树枝状大分子的试剂进行纯化。分析和 SE-HPLC 数据表明,螯合物与树枝状大分子的比率分别为 30:1 和 28:1。在 pH 7.4、22°C 和 3T 下测量的摩尔弛豫率是可比的(29.5 与 26.9 mM(-1)s(-1)),并且基于获得的图像,两种缀合物均同样适用于 MRI 造影剂。然而,大环试剂在体内的清除速度更快(t(1/2)=16 与 29 分钟)。我们的结论是,基于大环的试剂是更适合体内使用的试剂,原因是与 Gd(III)DOTA 络合物稳定性相关的动力学惰性相结合。