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Study of antitumor effect and mechanism of EGCG-PEG modified liposome for 67LR targeting

Research Project

Project/Area Number 15K18931
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Medical pharmacy
Research InstitutionIwate Medical University

Principal Investigator

Sugiyama Ikumi  岩手医科大学, 薬学部, 助教 (80509050)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywordsリポソーム / EGCG / ラミニンレセプター / 抗腫瘍効果
Outline of Final Research Achievements

We studied usability of (-)-epigallocatechin-3-gallate and polyethyleneglycol modified liposomal doxorubicin (EPL) for increase antitumor effect against high grade tumor cell with 67 kDa laminin receptor (67LR). EGCG-monoamine, novel EGCG-derivative was synthesized, was used as modified molecular on liposomal membrane. When tumor bearing mice which was subcutaneously planted on B16F10 mouse melanoma cells was administered EPL, antitumor effect of EPL was stronger than that of PEG modified liposomal doxorubicin (PL). Moreover, EPL became activated caspase-3 in tumor, namely it induced apoptosis by binding 67LR on tumor cells. In conclusion, it was expected that EPL was superior formulation for cancer treatment.

Report

(3 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • Research Products

    (6 results)

All 2016 2015

All Presentation (6 results) (of which Int'l Joint Research: 1 results)

  • [Presentation] カテキン受容体介在性リポソームの開発を目的としたEGCG誘導体の検討2016

    • Author(s)
      杉山育美、開發邦宏、加藤修雄、佐塚泰之
    • Organizer
      日本薬剤学会第 31 年会
    • Place of Presentation
      岐阜
    • Related Report
      2016 Annual Research Report
  • [Presentation] マウスメラノーマ細胞に対するEGCG-PEG修飾リポソ-ムの有用性2016

    • Author(s)
      杉山育美、開發邦宏、加藤修雄、佐塚泰之
    • Organizer
      第32回日本DDS学会学術集会
    • Place of Presentation
      静岡
    • Related Report
      2016 Annual Research Report
  • [Presentation] 標的指向性の増大を目的としたEGCGのリポソ-ム化2015

    • Author(s)
      杉山育美、佐塚泰之
    • Organizer
      第12回日本カテキン学会年次学術大会
    • Place of Presentation
      福岡
    • Year and Date
      2015-12-05
    • Related Report
      2015 Research-status Report
  • [Presentation] 抗腫瘍効果増強を目的としたEGCG誘導体の合成とリポソ-ム修飾2015

    • Author(s)
      杉山育美、佐塚泰之
    • Organizer
      第54回日本薬学会東北支部大会
    • Place of Presentation
      岩手
    • Year and Date
      2015-09-26
    • Related Report
      2015 Research-status Report
  • [Presentation] 67kDaラミニンレセプタ-を標的としたEGCG修飾リポソ-ムの体内動態におけるEGCG誘導体の検討2015

    • Author(s)
      杉山育美、開發邦宏、加藤修雄、佐塚泰之
    • Organizer
      第31回日本DDS学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2015-07-03
    • Related Report
      2015 Research-status Report
  • [Presentation] The Advanced Strategy of Novel EGCG Derivative Modified Liposome with High Targeting Ability to Tumor2015

    • Author(s)
      杉山育美、佐塚泰之
    • Organizer
      Annual Meeting 2015 of the American Association for Cancer Research
    • Place of Presentation
      Philadelphia
    • Year and Date
      2015-04-22
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research

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Published: 2015-04-16   Modified: 2018-03-22  

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