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量子ドットによる新規セラノスティックナノ粒子の開発

Research Project

Project/Area Number 18F18766
Research Category

Grant-in-Aid for JSPS Fellows

Allocation TypeSingle-year Grants
Section外国
Research Field Biomedical engineering/Biomaterial science and engineering
Research InstitutionNational Institutes for Quantum and Radiological Science and Technology

Principal Investigator

青木 伊知男  国立研究開発法人量子科学技術研究開発機構, 量子生命科学領域, 統括グループリーダー(定常) (10319519)

Co-Investigator(Kenkyū-buntansha) SEMKOVA SEVERINA  国立研究開発法人量子科学技術研究開発機構, 分子イメージング診断治療研究部・機能分子計測グループ, 外国人特別研究員
Project Period (FY) 2018-10-12 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2019: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2018: ¥400,000 (Direct Cost: ¥400,000)
Keywordstheranostics / quantum dots / nitroxide / imaging / redox / MRI / EPR
Outline of Annual Research Achievements

We developed new theranostic nanoparticles, based on quantum dots (QDs), conjugated with multispin nitroxide-cyclodextrins (QD@CD-TEMPO and QD@CD-TEMPOH) and triphenylphosphonium (TPP). Both sensors are applicable for quantitative imaging assays of oxidative stress and redox-status of living cells and tissues.
These nanoparticles combine several features: (i) three imaging modalities (MRI, EPR, optical); (ii) intracellular delivery and localization mainly into the mitochondria due to TPP; (iii) possibility to sense and visualize the areas of oxidative stress and redox-status in living cells and tissues – due to dynamics of their contrast properties, based on the balance between oxidizers and reducers; (iv) redox-modulating activity and possibility to induce apoptosis in cancer cells, without significant effect on viability of normal cells due to SOD-mimetic feature of nitroxide residues.
The analytical tests using both sensors were validated by conventional redox analyses (mitoSOX, DHE, DCF, TAC).
Both sensors were applied for:
1. EPR/optical imaging of oxidative stress and total reducing capacity in cultured cells with exogenously induced mitochondrial dysfunction. Cytotoxicity and induction of apoptosis on normal and cancer cells were also analysed (MTS assay, Annexin-V test).
2. MR imaging in animals with kidney dysfunction, induced by oxidative stress.

Research Progress Status

令和元年度が最終年度であるため、記入しない。

Strategy for Future Research Activity

令和元年度が最終年度であるため、記入しない。

Report

(2 results)
  • 2019 Annual Research Report
  • 2018 Annual Research Report
  • Research Products

    (4 results)

All 2019 2018 Other

All Int'l Joint Research (2 results) Journal Article (2 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 2 results)

  • [Int'l Joint Research] Trakia University/Sofia University/Bulgarian academy of science(ブルガリア)

    • Related Report
      2019 Annual Research Report
  • [Int'l Joint Research] Bulgarian Academy of Science/Sofia University/Torakia University(ブルガリア)

    • Related Report
      2018 Annual Research Report
  • [Journal Article] Resveratrol Modulates the Redox-status and Cytotoxicity of Anticancer Drugs by Sensitizing Leukemic Lymphocytes and Protecting Normal Lymphocytes2019

    • Author(s)
      IVANOVA DONIKA、ZHELEV ZHIVKO、SEMKOVA SEVERINA、AOKI ICHIO、BAKALOVA RUMIANA
    • Journal Title

      Anticancer Research

      Volume: 39 Issue: 7 Pages: 3745-3755

    • DOI

      10.21873/anticanres.13523

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] Loading Efficiency of Polymersomes with Contrast Agents and their Intracellular Delivery: Quantum Dots Versus Organic Dyes2018

    • Author(s)
      Semkova S, Nikolova B, Zhelev Z, Tsoneva I, Zlateva G, Aoki I, Bakalova R.
    • Journal Title

      Anticancer Research

      Volume: 38 Issue: 2 Pages: 825-831

    • DOI

      10.21873/anticanres.12290

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Int'l Joint Research

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Published: 2018-10-15   Modified: 2024-03-26  

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