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Design and synthesis of phosphatidylserine dimers with antitumor effect via the phagocytosis-inducing property

Research Project

Project/Area Number 25670048
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Drug development chemistry
Research InstitutionHokkaido University

Principal Investigator

SHUTO satoshi  北海道大学, 薬学研究科(研究院), 教授 (70241346)

Co-Investigator(Kenkyū-buntansha) FUKUDA Hayato  北海道大学, 薬学研究科(研究院), 助教 (30434450)
Co-Investigator(Renkei-kenkyūsha) ASAI Akira  静岡県立大学, 大学院薬学研究科, 教授 (60381737)
MATSUDA Tadashi  北海道大学, 薬学研究科(研究院), 教授 (20212219)
Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywordsホスファチジルセリン / ファゴサイトーシス / 二量等価体 / クアトロフェニル
Outline of Final Research Achievements

We designed and synthesized dimer derivatives of phosphatidylserine as phagocytosis inducer via exposure of phosphor-serine polar-head moieties on cell surface, which are potentially used in immune cancer therapy. We successfully synthesized these dimer derivatives. We demonstrated that the liposomes containing the synthesized dimer derivatives of phosphatidylserine actually exposed the phosphor-serine polar-head moieties on cell surface in the evaluation with tumor cells.

Report

(3 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • Research Products

    (1 results)

All 2015

All Presentation (1 results)

  • [Presentation] ファゴサイトーシス誘導性ホスファチジルセリン二量体類縁化合物の創製研究2015

    • Author(s)
      佐藤耀、川村周平、平尾徹、室元竜太、福田隼、阿部洋、松田正、周東智
    • Organizer
      日本薬学会第135年会
    • Place of Presentation
      神戸
    • Year and Date
      2015-03-25 – 2015-03-28
    • Related Report
      2014 Annual Research Report

URL: 

Published: 2014-07-25   Modified: 2019-07-29  

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