Impact of transporter-mediated drug absorption, distribution, elimination and drug interactions in antimicrobial chemotherapy
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抄録
金沢大学薬学部
金沢大学大学院自然科学研究科分子作用学
A comprehensive list of drug transporters has recently become available as a result of extensive genome analysis. Membrane transporters play important roles in determining the pharmacokinetic aspects of intestinal absorption, tissue distribution, and the urinary and biliary excretions of a wide variety of therapeutic drugs. The identification and characterization of transporters responsible for the transfer of nutrients and xenobiotics, including drugs, is expected to provide a scientific basis for understanding drug disposition, as well as the molecular mechanisms of drug-drug/drug-food/drug-protein interactions and inter-individual/inter-species differences. This review focuses on the influence of transporters on the pharmacokinetics of β-lactam antibiotics, new quinolones, and other antimicrobial agents, as well as focusing on the drug-drug interactions associated with transporter-mediated uptake from the small intestine and transporter-mediated elimination from the kidney and liver. © 2006 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases.
収録刊行物
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- Journal of Infection and Chemotherapy
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Journal of Infection and Chemotherapy 12 (5), 241-250, 2006-10-01
Springer Verlag
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詳細情報 詳細情報について
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- CRID
- 1050564285907311872
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- NII論文ID
- 10018348080
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- NII書誌ID
- AA11057978
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- ISSN
- 1341321X
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- IRDB
- CiNii Articles