^(125)I-MIL50在大鼠体内的药代动力学及生物分布  

Pharmacokinetics and Biodistribution of ^(125)I-MIL50 in Wistar Rats

作　　者：雷晓[1,2] 朱晓霞[2] 王德才[1] 孟志云[2] 甘慧[2] 顾若兰[2] 吴卓娜[2] 郑颖[2] 李俭[2] 吕明[3] 窦桂芳[2] 

机构地区：[1]泰山医学院,山东泰安271000 [2]军事医学科学院野战输血研究所,北京100850 [3]军事医学科学院基础医学研究所,北京100850

出　　处：《同位素》2016年第2期65-70,共6页Journal of Isotopes

基　　金：国家高技术研究发展计划项目(2012AA022001-05)

摘　　要：为探究^(125)I标记重组抗蓖麻毒素(Ricin)人源化单克隆抗体(^(125)I-MIL50)在大鼠体内的药代动力学、生物分布及排泄特点,采用Iodogen法对MIL50进行^(125)I标记,结合TCA法测定不同时间^(125)IMIL50在大鼠血清、组织、体液和排泄物中的含量。结果表明:Ricin染毒组和直接给药组血药浓度在14d内没有差异,14d后染毒组^(125)I-MIL50消除快于未染毒组;血清中^(125)I-MIL50浓度高于其他组织和体液,肾、膀胱组织中浓度较高,脑、脊髓、脂肪等脂性组织中浓度一直较低;^(125)I-MIL50给药后27d内经尿累积排泄率约为62.6%,经粪便的排泄率为15.5%。研究结果为临床实验和给药方案提供参考依据。In order to study the impact of Ricin on the pharmacokinetics of ^125I-MIL50 and to investigate the tissue distribution and excretion of ^125I-MIL50 in Wistar rats, MIL50 was labeled with ^125I using the Iodogen method. Then, the concentration of ^125I-MIL50 in serum, tissues, body fluids and excretions was measured by TCA method at different time. The results showed that ^25I-MIL50 was eliminated faster after 14 days in the Ricin administrated group. The concentration of ^125I-MIL50 in serum was always higher than that in other tissues. The level in kidney and bladder were high and in brain, spine and fat were low. The cumulative excretion rate of ^125I-MIL50 was 62.6% in urine, and 15.5% in feces within 27 days. Ricin could fasten the elimination of ^125I-MIL50 when the concentration of ^125 I-MIL50 was low in Wistar rats. It might because of the interaction between antigen and antibody, ^125I-MIL50 had no specific combination with tissues and it could hardly entered into lipophilic tissues. Urinary excretion represented the major pathway of elimination of ^125I-MIL-0. The results of the study provide a reference for clinical trials and drug administration program.

关 键 词：蓖麻毒素 ^125I-MIL50 药代动力学 生物分布 排泄 

分 类 号：TL923[核科学技术—核燃料循环与材料]