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一种新型三齿三羟吡啶酮的镓配合物用于潜在的核诊断成像:67Ga 标记物的溶液和体内研究。

A gallium complex with a new tripodal tris-hydroxypyridinone for potential nuclear diagnostic imaging: solution and in vivo studies of 67Ga-labeled species.

机构信息

Centro de Química Estrutural, Instituto Superior Técnico-UTL, 1049-001 Lisboa, Portugal.

出版信息

J Inorg Biochem. 2011 Jan;105(1):31-8. doi: 10.1016/j.jinorgbio.2010.09.012. Epub 2010 Oct 7.

Abstract

The gallium(III) complex of a new tripodal 3-hydroxy-4-pyridinone (3,4-HP) chelator has been studied in terms of its physico-chemical and in vivo properties aimed at potential application as probe for nuclear imaging. In particular, based on spectrophotometric titrations, the hexa-coordinated (1:1) gallium complex appeared as the major species in a wide physiological acid-neutral pH range and its high stability (pGa=27.5) should avoid drug-induced toxicity resulting from Ga(III) accumulation in tissues due to processes of transmetallation with endogenenous ligands or demetallation. A multinuclear ((1)H and (71)Ga) NMR study gave some insights into the structure and dynamics of the gallium(III) chelate in solution, which are consistent with the tris-(3,4-HP) coordination and an eventual pseudo-octahedral geometry. Biodistribution and scintigraphic studies of the (67)Ga(III) labelled chelate, performed in Wistar rats, confirmed the in vivo stability of the radiolabelled complex, its non interaction with blood proteins and its quick renal clearance. These results indicate good perspectives for potential application of extrafunctionalized analogues in radiodiagnostic techniques.

摘要

一种新的三齿 3-羟基-4-吡啶酮(3,4-HP)螯合剂的镓(III)配合物,在物理化学和体内性质方面进行了研究,旨在将其作为核成像探针进行潜在应用。特别是,基于分光光度滴定法,六配位(1:1)镓配合物在广泛的生理酸碱 pH 范围内表现为主要物种,其高稳定性(pGa=27.5)应避免由于 Ga(III)与内源性配体的转金属作用或脱金属作用而在组织中积累导致的药物诱导毒性。多核(^1H 和 ^71Ga)NMR 研究为溶液中镓(III)螯合物的结构和动力学提供了一些见解,这与三-(3,4-HP)配位和最终的拟八面体几何结构一致。在 Wistar 大鼠中进行的(^67Ga(III)标记螯合物的生物分布和闪烁显像研究证实了放射性标记配合物的体内稳定性、与血液蛋白的非相互作用以及快速的肾脏清除。这些结果表明,在放射性诊断技术中,具有额外功能化类似物的镓(III)配合物具有良好的应用前景。

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