Distribution and Excretion of Radioactivity Following Intraportal Administration of $^{166}$ 7Ho-Chitosan Complex to Rats

흰쥐의 간문맥으로 투여한 $_{166}$ Holmium-chitosan의 분포와 배설

  • BAEK, Min Sun (Doping Control Center, Korea Institute of Science and Technology) ;
  • PARK, Kyung Bae (Korea Advanced Energy Research Institute) ;
  • KIM, Dong Hyun (Doping Control Center, Korea Institute of Science and Technology)
  • 백민선 (한국과학기술연구원, 토핑콘트롤센터) ;
  • 박경배 (한국원자력 연구소) ;
  • 김동현 (한국과학기술연구원, 토핑콘트롤센터)
  • Published : 1997.09.01

Abstract

The distribution and excretion of radioactivity were examined after intraportal administration of sup 166/Ho-chitosan complex at a dose of 1 mcitg (10 mg chitosan/kg) to rats. Whole body macroautoluminographs showed that the radioactivity after an administration was concentrated in liver and perfused primarily to organs including kidney, spleen, and bone marrow, then to muscle and brain. Similar profiles were observed from 2 hr to 168 hr after the administration. The relative percentage of radioactivity in bone and spinal column increased with time, suggesting that free $^{166}$ Ho, released from chitosan complex deposited in the liver, selectively binds to these tissues. $^{166}$ Ho-chitosan complex administered intraportally was excreted less than 4% through urine (2.7$\pm$0.8%) and feces (0.65 $\pm$ 0.4%) up to seven days. These results demonstrate that the radio-activity of $_{166}$ Ho-chitusan complex when administered intraportally, mainly localizes in liver without affec-ting other tissues and organs. Considering the short half life of $^{166}$ Ho and the localization to the liver, $^{166}$ Ho-chitosan complex might be a useful agent in the treatment of hepatic carcinoma.

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