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Analysis of drug disposition in the central nervous system based on the transport characteristics across the blood-brain barrier and blood-cerebrospinal fluid barrier : Special focus on Peptide

Research Project

Project/Area Number 04452303
Research Category

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

Allocation TypeSingle-year Grants
Research Field Physical pharmacy
Research InstitutionUniversity of Tokyo

Principal Investigator

SUGIYAMA Yuichi  Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Professor, 薬学部, 教授 (80090471)

Co-Investigator(Kenkyū-buntansha) SUZUKI Hiroshi  Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Research Associ, 薬学部, 助手 (80206523)
Project Period (FY) 1992 – 1993
Project Status Completed (Fiscal Year 1993)
Budget Amount *help
¥4,900,000 (Direct Cost: ¥4,900,000)
Fiscal Year 1993: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1992: ¥4,000,000 (Direct Cost: ¥4,000,000)
KeywordsBlood-Brain Barrier / Blood-CSF Barrier / Peptide / New quinolone / Anti-AIDS drug / Physiological Pharmacokinetics / 血液脳関門 / 能動輸送 / 担体輸送 / 血液・脳関門 / 血液・脳脊髄液関門 / 脳毛細血管内皮細胞 / 脈絡叢上皮細胞 / 薬物速度論
Research Abstract

[1] Inhibition of active efflux of anticancer drugs from cancer cells :
The kinetic analysis of active efflux of anticancer drug, vincristine (VCR), from isolated rat hepatocytes (normal cells) and P-388 cells (cancer cells) was examined, especially focused on the effect of various inhibitors. As a results, (1)After being taken up by the cells, vincristine was either effluxed from the cells in an active transport manner or transferred into the intracellular deep pool compartment. These two roots are competitive pathway. Our study revealed that inhibitors such as verapamil and cyclosporin inhibit only the former pathway. (2) By comparing the inhibitory extent between normal and cancer cells, it has been demonstrated that many inhibitors have higher affinity for P-glycoprotein on the surface membrane of cancer cells than that for one of normal cells, suggesting that these inhibitors possibly can be used as a anticancer drug even in in vivo situation
[2]Kinetic analysis of in vivo disposition of monoclonal antibody against P-glycoprotein :
In vivo disposition and in vitro kinetics of monoclonal antibody against P-glycoprotein, MRK-16, was examined with HCT-15 cells (resistant cells) and Colo Cells (sensitive cells). The amount of surface bound, internalized, and medium were determined with time, and the obtained data were fitted to the appropriate mathematical model to calculate the kinetic parameters. Analysis based on the physiological pharmacokinetic model revealed that the distribution of this antibody after i.v.administration to mice was well-predicted using thus obtained kinetic parameters. From our findings, it is clearly demonstrated that not only expression amount of the P-glycoprotein on the surface of the cancer cells, but the permeability across the capillary endotherial cells of antibody are the important factor to determine the in vivo disposition of the antibody.

Report

(3 results)
  • 1993 Annual Research Report   Final Research Report Summary
  • 1992 Annual Research Report
  • Research Products

    (5 results)

All Other

All Publications (5 results)

  • [Publications] 杉山雄一.大家毅: "In vitro試験管内でのデータを基にした薬物体内動態の予測" ファーマコキネティクス研究の方法と技術. 87-108 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] 鈴木洋史: "血液脳関門透過の評価法:in vivo系,潅流系,単離・培養細胞系での解析" ファーマコキネティクス研究の方法と技術. 227-244 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] Yuichi Sugiyama and Tsuyoshi Ooie: "Prediction of drug disposition with the in vitro data" The methods and technique in pharmacokinetics. 87-108 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] Hiroshi Suzuki: "Evaluation of permeability across the blood-brain barrier : Analysis in in vivo, brain perfusion, isolated and cultured cells" The methods and technique in pharmacokinetics. 227-244 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] 鈴木 洋史: "血液・脳関門透過の評価法:in vitro系,潅流系,in vivo系での評価" 薬物動態研究の方法とその技術. (1993)

    • Related Report
      1992 Annual Research Report

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Published: 1992-04-01   Modified: 2016-04-21  

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