Physiological and Anatomical Factors Controlling Intestinal Drug Absorption Mechanism
Physiological and Anatomical Factors Controlling Intestinal Drug Absorption Mechanism
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
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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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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通讯作者:
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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Hideaki Takahashi.: J.Pharm.Pharmacol. 40. 252-257 (1988)
高桥英明:J.Pharm.Pharmacol。
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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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Masahiro Hayashi: "Modern Biopharmaceutics" Shoji Awazu and Tamaotsu Koizumi (eds.). Nankodo. 29-46 (1991)
Masahiro Hayashi:《现代生物制药》Shoji Awazu 和 Tamaotsu Koizumi(编)。
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共 18 条
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Improvement of intestinal drug absorption based on structural changes of tight junction and functional changes of P-glycoprotein
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General research project of linguistic movements and language policies aiming at multilingual societies
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批准号:13410056
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财政年份:2001
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依托单位:
Intestinal Drug Absorption and Excretion-Detoxication Using Regulation of Membrane Permeation by Oligopeptide-produced Neutrophils
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财政年份:1999
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依托单位:
Development of in vitro screening system for CYP based drug interaction
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Physiological and Biochemical Assessment of Membrane Barrier Function in Inflammatory Disease
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依托单位:
Membrane Permeability and Its Improvement in Intestinal Absorption of Macromolecular Drugs
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批准号:03671103
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.34万
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负责人:HAYASHI Masahiro
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依托单位: