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首页> 外文期刊>Bulletin of the Korean Chemical Society >Gadolinium Complex of 1,4,7,10-Tetraazacyclododecane-1,4,7-trisacetic acid (DO3A) Conjugate of [(p-aniline benzothiazole)methyl]pyridine as a Tumor-Targeting MRI Contrast Agent
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Gadolinium Complex of 1,4,7,10-Tetraazacyclododecane-1,4,7-trisacetic acid (DO3A) Conjugate of [(p-aniline benzothiazole)methyl]pyridine as a Tumor-Targeting MRI Contrast Agent

机译:1,4,7,10-四氮杂环十二烷-1,4,7-三乙酸(DO3A)[配合物[( p -苯胺苯并噻唑)甲基]吡啶作为靶向肿瘤的MRI对比代理商

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The synthesis of a DO3A conjugate of [(p-aniline benzothiazole)methyl]pyridine (L2H3) and its gadolinium complex of the type [Gd(L2)(H2O)] (GdL2) is described. The R1 relaxivity (= 4.50 mM−1sec−1) and kinetic inertness of GdL2 compares well with those of structurally analogous Dotarem® (R1 = 3.70 mM−1sec−1), a typical extracellular (ECF) MRI contrast agent (CA). Yet, by comparison with Dotarem®, GdL2 exhibits noncovalent interactions with human serum albumin (HSA) as evidenced by the ε* titration curve along with in vivo MR signal enhancement in both aorta and heart. Liver-specific nature of GdL2 is also observed as excretion is made through gallbladder. Most notably, GdL2 further demonstrates specificity toward the MDAMB- 231 breast cancer.
机译:描述了[(对苯胺苯并噻唑)甲基]吡啶(L2H3)及其类型为[Gd(L2)(H2O)](GdL2)的DO配合物的DO3A共轭物的合成。 GdL2的R1弛豫度(= 4.50 mM-1sec-1)和动力学惰性与结构类似的Dotarem®(R1 = 3.70 mM-1sec-1)(一种典型的细胞外(ECF)MRI造影剂(CA))相比较。然而,通过与Dotarem®的比较,GdL2与人血清白蛋白(HSA)表现出非共价相互作用,这由ε*滴定曲线以及主动脉和心脏的体内MR信号增强所证明。还可以观察到GdL2的肝脏特异性,因为它是通过胆囊排泄的。最值得注意的是,GdL2进一步显示出对MDAMB-231乳腺癌的特异性。

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