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作 者:张俊波[1] 任佳蕾[1] 林艳[1] 王学斌[1]
机构地区:[1]北京师范大学化学学院放射性药物教育部重点实验室,北京100875
出 处:《北京师范大学学报(自然科学版)》2007年第4期423-426,共4页Journal of Beijing Normal University(Natural Science)
基 金:国家自然科学基金青年基金资助项目(20201004);北京市科技新星计划资助项目(2004A20);北京市优秀人才培养基金资助项目(20042D0503101)
摘 要:采用fac-[99mTc(CO)3(H2O)3]+与N-甲基-N-环己基氨荒酸盐(MECHDTC)在室温下发生配体交换反应制得99mTc(CO)3-MECHDTC配合物.用薄层层析(TLC)法和高效液相色谱(HPLC)法鉴定该配合物的放射化学纯度(R)大于90%.该配合物是一种体外稳定性良好的脂溶性电中性物质.99mTc(CO)3-MECHDTC配合物和99mTcN-MECHDTC配合物在小鼠体内生物分布结果表明,前者在小鼠心肌和脑中摄取量均较低且明显低于后者,说明在MECHDTC配体中并不适合引入[99mTc(CO)3]+核.The organometallic precursor fac-[^99mTc(CO)3(H2O)3]^+ is reacted with N-methyl, N-cyclohexyl dithiocarbamate (MECHDTC) at room temperature to produce the ^99mTc(CO)3-MECHDTC complex. The radiochemical purity (RCP) of the product is over 90% as measured by thin layer chromatography (TLC) and by high performance liquid chromatography (HPLC). No decomposition of the complex at room temperature (RT) is observed over a period of 6 h. The complex is neutral and lipophilic, and has good stability at room temperature. The biodistribution comparisons in mice of the ^99mTc(CO)3-MECHDTC complex and the ^99mTcN(MECHDTC)2 complex show that the former has a much lower heart and brain uptake as compared to that of the latter, suggesting the incorporation of the [^99mTc(CO)3]^+ core into the MECHDTC ligand is not suitable to develop new better diagnostic agents.
关 键 词:锝-99m [^99mTc(CO)3]^+核 氨荒酸盐 生物分布
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