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The Application of ^<203>Pb for Radiopharmaceuticals

Research Project

Project/Area Number 01570585
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Radiation science
Research InstitutionKanazawa University

Principal Investigator

ANDO Atsushi  Kanazawa University, school of Allied Medical Professions, Professor, 医療技術短期大学部, 教授 (50019915)

Co-Investigator(Kenkyū-buntansha) YAGI Kazuo  Kanazawa University, school of Allied Medical Professions, Instructor, 医療技術短期大学部, 助手 (50201819)
ANDO Itsuko  Kanazawa University, school of Allied Medical Professions, Instructor, 医療技術短期大学部, 助手 (60211017)
Project Period (FY) 1989 – 1990
Project Status Completed (Fiscal Year 1990)
Budget Amount *help
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1990: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1989: ¥1,100,000 (Direct Cost: ¥1,100,000)
KeywordsPb-203 / Ga-67 / Tl-201 / Radiopharmaceutical / Tumor imaging agent / Tlー203 / 悪性腫瘍陽性描画剤 / Pb-203 / 悪性腫瘍陽性描画
Research Abstract

The radionuclide ^<203>Pb decays completely by electron capture to stable ^<203>Tl with a halfーlife of 52 hours. The present study was undertaken to investigate the application of ^<203>Pb for radiopharmaceuticals (especially tumor imaging agent).
^<203>Pbーchloride solution was injected into the tumorーbearing rats, tumor-bearing mice and inflammatoryーinduced rats. These animals were killed at various time intervals from 3 hours to 48 hours. Tumor tissue and normal tissues were excised. The retention values of ^<203>Pb in the tissues were calculated against the administered dose of ^<203>Pb. The results obtained from the experiments about ^<203>Pbーcholoride were compared with previously described results of ^<67>Gaーcitrate and ^<201> Tlーchloride. In addition, bio-distribution of ^<203>Pb in animal body was observed by whole body autoradiography and that of this nuclide in tumor tissue was observed by macro-auto-radiography. Subcellular distribution of ^<203>Pb in tumor tissue was determined by the modified method of Hogeboom and Schneider.
Retention values of ^<203>Pb in tumor tissue was smaller than those for ^<67>Ga, and much larger than those for ^<201>Tl. But retention values of ^<203>Pb in inflammatory tissue were smaller than those for ^<67>Ga and ^<201>Tl. The avid uptake of ^<203>Pb in bone and the uptake of this nuclide in tumor and liver were observed by whole body autoradiography. Accumulation of this nuclide in viable tumor tissue was observed by macroautoradiography.
From the results described above, it was deduced that ^<203>Pbーchloride was a potential tumor imaging agent which hardly accumulated in inflammatory tissue.

Report

(3 results)
  • 1990 Annual Research Report   Final Research Report Summary
  • 1989 Annual Research Report
  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] 安東 醇: "Pbー203 chlorideのがん親和性" 核医学. 26. 701 (1989)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] 安東 醇: "塩化鉛(Pbー203)の悪性腫瘍および炎症巣への集積" 日本薬学会第110年会講演要旨集. 4. 233 (1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Ando, Atsushi: "Tumor affinity of Pbーchloride (Pb-203)" Jpn. J. Nucl. Med.vol. 26. 701 (1989)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Ando, Atsushi: "Accumulation of read (11) chloride (Pbー203) in malignant tumor and inflammatory lesion" Abstract Book of the 110th Annual Meeting of the Pharmaceutical Society of Japan. 4. 233 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] 安東 醇: "塩化鉛(Pbー203)の悪性腫瘍および炎症巣への集積" 日本薬学会第110年会講演要旨集. 4. 233 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] 安東醇: "塩化鉛(Pb-3203)の癌および臓器親和性" 核医学. 26. 1080 (1989)

    • Related Report
      1989 Annual Research Report

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Published: 1989-04-01   Modified: 2016-04-21  

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