摘要
利用放射性元素153Gd合成153Gd-DTPA,经小鼠尾静脉注射后,取5、15、30、60、120、180min六个时相处死小鼠,解剖,测量各脏器放射性计数,计算得到不同时相153Gd-DTPA在各脏器的分布情况。血药清除符合二室模型,t1/2(1)=1.5min、t1/2(2)=29.9min,尿液中药物排泄量t1/2=16min,3h时药物90%量在膀胱中。该药物主要通过肾脏代谢,其余脏器摄取甚少。通过153Gd-DTPA动物实验研究得到了Gd-DTPA的药代动力学数据。
Gd-DTPA was synthesized by 153GdCl3 and DTPA.The mice killed and biodistribution of the organs measured at 5,15,30,60,120 and 180 min post-injection. Blood 153Gd-DTPA clearence curve conformed a two-compartment open model,t1/2(1)= 1.smin,t1/2(2)= 29.gmin. Determination of urine 153Gd-DTPA concentration find: t1/2=16min.Within three hours,90 percent of the drug was concentrated in urine, thereby mainly excreated through kidney.
出处
《核技术》
CAS
CSCD
北大核心
1995年第5期278-281,共4页
Nuclear Techniques
关键词
钇153
小鼠
DTPA
药代动力学
核磁共振成像
Contrast-enhancing agent,Gadolinium-diethylenetriamine pentaacetic acid,153Gd,Pharmacokinetic