Knapp F F, Ambrose K R, Callahan A P, Ferren L A, Grigsby R A, Irgolic K J
J Nucl Med. 1981 Nov;22(11):988-93.
A series of Te-123m-labeled fatty acids has been synthesized and studied in rats. In the series of compounds studied, the position of the Te-123m heteroatom was not as important as the total chain length, which dramatically affected the heart uptake. Five minutes after injection, significant heart uptake (1.7-2.3% of injected dose) was observed for agents with C15, C17, and C21 chain lengths, in which Te-123m replaced a methylene group in either the 6, 9, 11, or 17 positions, and the heart-to-blood ratios were high. An important observation was the prolonged retention of radioactivity for at least one hour after injection. In contrast, agents with shorter C13 chain lengths, with Te-123m in either the 6 or the 9 position, exhibited only low heart uptake (0.1-0.3% of injected dose).
已合成了一系列用锝-123m标记的脂肪酸,并在大鼠身上进行了研究。在所研究的一系列化合物中,锝-123m杂原子的位置不如总链长重要,总链长对心脏摄取有显著影响。注射后五分钟,观察到碳链长度为C15、C17和C21的化合物有显著的心脏摄取(占注射剂量的1.7 - 2.3%),其中锝-123m取代了6、9、11或17位的亚甲基,且心脏与血液的比率较高。一个重要的观察结果是注射后放射性至少持续保留一小时。相比之下,碳链长度较短的C13化合物,锝-123m位于6或9位,仅表现出较低的心脏摄取(占注射剂量的0.1 - 0.3%)。