Bryant L H, Brechbiel M W, Wu C, Bulte J W, Herynek V, Frank J A
Laboratory of Diagnostic Radiology Research (CC), National Institutes of Health, Bethesda, Maryland 20892, USA.
J Magn Reson Imaging. 1999 Feb;9(2):348-52. doi: 10.1002/(sici)1522-2586(199902)9:2<348::aid-jmri30>3.0.co;2-j.
A series of high-generation (G) ethylenediamine-core polyamidoamine (PAMAM) dendrimers corresponding to G = 5, 7, 9, and 10 were conjugated with the bifunctional chelate 2-(4-isothiocyanatobenzyl)- 1,4,7,10-tetraazacyclododecane-N,N',N",N"'-tetraacetate (p-SCN-Bz-DOTA). Gadolinium (III) ion was added to the macromolecules, and the 1/T1 and 1/T2 NMRD profiles were measured at 3 degrees, 23 degrees, and 37 degrees C. The synthesis resulted in preparations that ranged from an average of 127 chelates and 96 Gd3+ ions per G = 5 dendrimer to an average of 3727 chelates and 1860 Gd3+ ions per G = 10 dendrimer. At 20 MHz and 23 degrees C, the 1/T1 ion relaxivity increased from 30 mM(-1) s(-1) for the G = 5 to 35 mM(-1) s(-1) for the G = 7 PAMAM dendrimer-DOTA-Gd, reaching a plateau at 36 mM(-1) s(-1) for the G = 9 and G = 10 dendrimers. A similar plateau was observed for 1/T2 with values of 36 mM(-1) s(-1) for G = 5, 42 mM(-1) s(-1) for G = 7, and 45 mM(-1) s(-1) for the G = 9 and G = 10 dendrimers. This "saturation" of ion relaxivity for high-generation dendrimers occurred over the entire frequency range studied. The 1/T1 and 1/T2 relaxivities decreased as the temperature decreased for each generation of dendrimer studied, implying that slow water exchange of bound water molecules with the bulk solvent limits the relaxivity. In such circumstances, increases in the rotational correlation time of the macromolecules associated with higher generations of dendrimer does not result in significant increases in the ion relaxivity. Although the ion relaxivity does not increase, the total molecular relaxivities increased from 2880 mM(-1) s(-1) to 66960 mM(-1) s(-1) for the G = 5 to the G = 10 dendrimer. The current findings are relevant for the design of high-generation dendrimer-based receptor agents.
一系列高代数(G)的以乙二胺为核的聚酰胺-胺(PAMAM)树枝状大分子,对应G = 5、7、9和10,与双功能螯合剂2-(4-异硫氰酸苄基)-1,4,7,10-四氮杂环十二烷-N,N',N",N"'-四乙酸(p-SCN-Bz-DOTA)进行共轭。向大分子中加入钆(III)离子,并在3℃、23℃和37℃下测量1/T1和1/T2核磁共振弛豫分散(NMRD)曲线。合成得到的制剂范围从每个G = 5树枝状大分子平均含127个螯合物和96个Gd3+离子到每个G = 10树枝状大分子平均含3727个螯合物和1860个Gd3+离子。在20 MHz和23℃下,1/T1离子弛豫率从G = 5的30 mM-1 s-1增加到G = 7的PAMAM树枝状大分子-DOTA-Gd的35 mM-1 s-1,对于G = 9和G = 10树枝状大分子在36 mM-1 s-1处达到平稳状态。对于1/T2也观察到类似的平稳状态,G = 5的值为36 mM-1 s-1,G = 7为42 mM-1 s-1,G = 9和G = 10树枝状大分子为45 mM-1 s-1。高代数树枝状大分子的离子弛豫率的这种“饱和”现象在所研究的整个频率范围内都出现。对于所研究的每一代树枝状大分子,随着温度降低,1/T1和1/T2弛豫率都降低,这意味着结合水分子与大量溶剂之间的缓慢水交换限制了弛豫率。在这种情况下,与更高代数树枝状大分子相关的大分子旋转相关时间的增加并不会导致离子弛豫率显著增加。尽管离子弛豫率没有增加,但从G = 5到G = 10树枝状大分子,总分子弛豫率从2880 mM-1 s-1增加到66960 mM-1 s-1。当前的研究结果与基于高代数树枝状大分子的受体剂的设计相关。