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Physiological and Anatomical Factors Controlling Intestinal Drug Absorption Mechanism

Physiological and Anatomical Factors Controlling Intestinal Drug Absorption Mechanism
控制肠道药物吸收机制的生理和解剖因素
批准号:
63571101
负责人:
HAYASHI Masahiro
金额:
$1.47万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1988
资助国家:
日本
项目状态:
已结题
起止时间:
1988 至 1990

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中文摘要
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英文摘要
As two factors controlling drug absorption mechanism, permeation routes and blood flow dependence were analyzed. The colonic and jejunal absorption of poorly-absorbed cefmetazole were enhanced by sodium caprate (C10) in the rat. Its enhancing effects was greater in the colon than in the jejunum.For the intercellular (paracellular) pathways in the colon, C10 increased the equivalent pore radii ; C10 increased permeability through large and small pores which was obtained from the relationship between the membrane permeability of water-soluble non-electrolytes with various molecular weights and their free diffusion coefficients. Impedance analysis showed that C10 decreased the junctional resistance and increased the membrane capacitance, supporting the increase in junctional leakiness and the enlargement of intercellular space. For the intercellular pathways in the jejunum, no C10 effect was found. The similar site-dependent enhancement was observed also by the voltage clamp method.For th … More e transcellular pathway, fluorescence polarization technique showed that membrane perturbation through the interaction between C10 and membrane protein or lipids enhances the membrane permeability. Transcellular permeability increased by C10 was greater in the jejunum than in the colon. Consequently, the difference between the effects of C10 on the jejunal and colonic absorption of cefmetazole was considered to be due mainly to the difference in its effects on the intercellular pathway.For the blood flow dependent drug absorption, simultaneous luminal and vascular perfusion using the perfluorochemical emulsion as a vascular perfusate was examined. This emulsion was found to retain its normal barrier functions for drug transport. The contribution of blood flow resistance to total resistance of antipyrine absorption exceeded that for salicylic acid absorption. The effects of albumin the vascular perfusate on drug absorption is now under investigation from the direct action of albumin on the capillary wall. Less
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会议论文
Toyohiro Sawada: "Paracellular Channel Characterized by Nonーelectrolyte Permeation through the Colonic Membrane of the Rat" J.PharmacobioーDyn.12. 634-639 (1989)
Toyohiro Sawada:“以非电解质渗透通过大鼠结肠膜为特征的细胞旁通道”J.PharmacobioDyn.12 634-639 (1989)。
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林 正弘(伊賀 立二,奥村 勝彦編集): "生物薬剤学ー最近の進歩" 薬業時報社, 433 (1989)
Masahiro Hayashi(由 Tatsuji Iga 和 Katsuhiko Okumura 编辑):“生物制药 - 最近进展”Yakugyo Jihosha,433 (1989)
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通讯作者:
Hideaki Takahashi.: J.Pharm.Pharmacol. 40. 252-257 (1988)
高桥英明:J.Pharm.Pharmacol。
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通讯作者:
Masahiro Hayashi: "Advances in Biopharmaceutics" Tatsji Iga and Katsuhiko Okumura (eds.). Yakugyojihosha. 31-44 (1989)
Masahiro Hayashi:“生物制药的进展”Tatsji Iga 和 Katsuhiko Okumura(编辑)。
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18
    Investigation on failures of RNA editing and immune system againstviral infection in dyschromatosis symmetrica hereditaria
    • 批准号:
      23791252
    • 项目类别:
      Grant-in-Aid for Young Scientists (B)
    • 资助金额:
      $2.66万
    • 财政年份:
      2011
    • 负责人:
      HAYASHI Masahiro
    • 依托单位:
    Improvement of inflammatory bowel diseases based on expression and functional changes of P-glycoprotein by methylpredonislone and essential fatty acids
    New Prediction System of Infective Disease Based on Changes in Expression and Function of ABC Transporter
    Improvement of intestinal drug absorption based on structural changes of tight junction and functional changes of P-glycoprotein