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一种以脂肪族硫醇作为共配体的新型“3 + 1”混合配体99mTc配合物的合成、表征及生物学评价

Synthesis, characterization and biological evaluation of a novel "3 + 1" mixed ligand 99mTc complex having an aliphatic thiol as coligand.

作者信息

Rey A, Papadopoulos M, Leon E, Mallo L, Pirmettis Y, Manta E, Raptopoulou C, Chiotellis E, Leon A

机构信息

Cátedra de Radioquímica, Facultad de Química, Montevideo, Uruguay.

出版信息

Appl Radiat Isot. 2001 Mar;54(3):429-34. doi: 10.1016/s0969-8043(00)00285-2.

Abstract

A novel "3 + 1" mixed ligand 99mTc complex with N,N-bis(2-mercaptoethyl)-N'N'-diethyl-ethilenediamine as ligand and 1-octanethiol as coligand was prepared and evaluated as potential brain radiopharmaceutical. Preparation at tracer level was accomplished by substitution, using 99mTc-glucoheptonate as precursor and a coligand/ligand ratio of 5. Under these conditions the labeling yield was over 80% and a major product with radiochemical purity >80% was isolated by HPLC methods and used for biological evaluation. Chemical characterization at carrier level was developed using the corresponding rhenium and 99gTc complexes. Results were consistent with the expected "3 + 1" structure and X-ray diffraction study demonstrated that the complex adopted a distorted trigonal bipyramidal geometry. All sulphur atoms underwent ionization leading to the formation of a neutral compound. Biodistribution in mice demonstrated early brain uptake, fast blood clearance and excretion through hepatobiliary system. Although brain/blood ratio increased significantly with time, this novel 99mTc complex did not exhibit ideal properties as brain perfusion radiopharmaceutical since brain uptake was too low.

摘要

制备了一种新型的“3 + 1”混合配体99mTc配合物,以N,N-双(2-巯基乙基)-N',N'-二乙基亚乙基二胺为配体,1-辛硫醇为共配体,并将其作为潜在的脑放射性药物进行评估。在示踪剂水平下,以99mTc-葡庚糖酸盐为前体,共配体/配体比例为5,通过取代反应完成制备。在这些条件下,标记产率超过80%,通过高效液相色谱法分离出放射化学纯度>80%的主要产物,并用于生物学评估。在载体水平上,使用相应的铼和99gTc配合物进行化学表征。结果与预期的“3 + 1”结构一致,X射线衍射研究表明该配合物采用扭曲的三角双锥几何结构。所有硫原子均发生电离,形成中性化合物。在小鼠体内的生物分布表明,该配合物早期脑摄取、血液清除快且通过肝胆系统排泄。尽管脑/血比随时间显著增加,但由于脑摄取过低,这种新型99mTc配合物作为脑灌注放射性药物并未表现出理想的性质。

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