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In-cell synthesis of anticancer drugs from non-toxic precursor compounds by monochromatic X-ray irradiation

Research Project

Project/Area Number 16K12910
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Medical systems
Research InstitutionTokyo Institute of Technology

Principal Investigator

Oguri Yoshiyuki  東京工業大学, 科学技術創成研究院, 教授 (90160829)

Co-Investigator(Kenkyū-buntansha) 羽倉 尚人  東京都市大学, 理工学部, 准教授 (00710419)
Project Period (FY) 2016-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2017: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2016: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Keywordsガン治療 / 化学療法 / 抗ガン剤 / 放射線分解 / X線吸収端 / 陽子線励起単色X線 / 加速器 / 高速液体クロマトグラフィー / 陽子線励起準単色X線 / 浸潤性ガン治療 / 低侵襲治療 / 単色X線 / X線吸収端 / 陽子線 / 静電加速器 / 注射針 / X線増感剤 / 放射線 / 癌 / 量子ビーム / X線
Outline of Final Research Achievements

We investigated the feasibility of a cancer chemotherapy based on in-cell synthesis of anti-cancer drugs from non-toxic precursor compound by X-ray irradiation using a syringe-needle-type proton-induced monochromatic X-ray source inserted into the tumor. The dependence of the yield of decomposition products on the incident X-ray energy was measured using monochromatic X-rays with different energies around the absorption edge of the metallic element in the precursor material. As a result, it was confirmed that even if the absorbed dose was the same, the yield of some specific decomposition products was higher when the X-ray energy exceeded the absorption edge energy. From this result, we found that a minimally invasive treatment for synthesizing anticancer drugs only inside cancer cells is possible in principle, if an energy-optimized proton-induced monochromatic X-ray is used for irradiation of the precursor compound.

Academic Significance and Societal Importance of the Research Achievements

ガンの化学療法に伴う副作用を,低線量の放射線化学反応を用いて根本的に解決する方法を提案し,その原理的実証を行った.従来,放射線化学反応の収量は,物質へのエネルギー付与を基準に議論されてきたが,これに加えて物質を構成する元素の低エネルギー領域におけるX線吸収端構造を考慮して収量の光子エネルギー依存性に注目した.この手法に必要な高性能単色X線源の開発,線量の精密評価,動物実験等による検証,さらに適切な高選択性を持つ抗ガン剤前駆物質の開発が進めば,低線量のX線照射だけで無害の原料物質からガン細胞内部に限定して抗ガン剤を合成できるため,原理的には患者への負担が大幅に軽減される.

Report

(5 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (5 results)

All 2017 2016 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (1 results) (of which Int'l Joint Research: 1 results) Remarks (3 results)

  • [Journal Article] Evaluation of the X-ray distribution of a syringe-needle type proton-induced X-ray source by Geant4 simulation2017

    • Author(s)
      Hu Y.、Fukuda H.、Oguri Y.
    • Journal Title

      X-Ray Spectrometry

      Volume: 46 Issue: 5 Pages: 356-360

    • DOI

      10.1002/xrs.2785

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Presentation] Evaluation of the X-ray distribution of a syringe-needle type proton-induced X-ray source by Geant4 simulation2016

    • Author(s)
      Y. Hu, H. Fukuda and Y. Oguri
    • Organizer
      European Conference on X-ray Spectrometry 2016
    • Place of Presentation
      Gothenburg, Sweden
    • Year and Date
      2016-06-19
    • Related Report
      2016 Research-status Report
    • Int'l Joint Research
  • [Remarks] 研究テーマ:陽子線励起準単色X線の医学利用

    • URL

      http://www.lane.iir.titech.ac.jp/~yoguri/

    • Related Report
      2019 Annual Research Report
  • [Remarks] X線吸収端を用いた被ばく線量の少ないX線診断・治療技術の基礎研究

    • URL

      http://www.nr.titech.ac.jp/~yoguri/research/research.html

    • Related Report
      2018 Research-status Report
  • [Remarks] 小栗研究室 ― 研究室紹介 #38 ―

    • URL

      https://educ.titech.ac.jp/ee/news/2016_10/052795.html

    • Related Report
      2017 Research-status Report

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Published: 2016-04-21   Modified: 2021-02-19  

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