Absorption, Biliary Excretion, and Metabolism of a New Cholelitholytic Agent, Ursodeoxycholyl N-Carboxymethylglycine and Its Esters in Rats
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- HATONO Shunso
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- YOSHIDA Harumi
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- MATSUNAMI Masumi
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- IDE Yukako
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- MATSUDA Kaoru
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- YATSUNAMI Takashi
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- FUWA Tohru
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- KIHIRA Kenji
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- KURAMOTO Taiju
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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- HOSHITA Takahiko
- Wakunaga Pharmaceutical Co., Ltd. Institute of Pharmaceutical Sciences, Hiroshima University School of Medicine
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抄録
Intestinal absorption, biliary excretion and metabolism of a calcium gallstone dissolving agent, [11,12-^3H] ursodeoxycholyl-N-carboxymethylglycine (UDC-CMG) and its monoethyl, diethyl and dipivaloyloxyethyl esters (UDC-CMG-Et, UDC-CMG-Et_2 and UDC-CMG-PV_2) were studied in bile duct cannulated rats. Biliary recovery of [^3H]-labeled UDC-CMG, UDC-CMG-Et and UDC-CMG-Et_2 after intraduodenal administration were 65%, 80%, 98%, respectively. Radio-thin layer chromatography analysis of the bile revealed that UDC-CMG didn't undergo any biotransformation during administration and excretion. About 80% and 20% of radioactivity recovered in the bile was identified as UDC-CMG-Et and UDC-CMG, respectively, after intraduodenal administrations of [^3H] UDC-CMG-Et_2 and [^3H] UDC-CMG-Et. The administered intact UDC-CMG-Et_2 was not found in the bile. Intraduodenally administered [^3H] UDC-CMG-PV_2 was rapidly recovered in the bile. The total recovery rate was 78% within a 24 h period. More than 80% of the radioactivity recovered in the bile was found as UDC-CMG. Lesser amounts of the monopivaloyloxyethyl ester of UDC-CMG were also found, but intact UDC-CMG-PV_2 was not detected in the bile as in the case of UDC-CMG-Et_2. Among the esters of UDC-CMG investigated in the present studies, only UDC-CMG-PV_2 was excreted in the bile mainly as the perhydrolyzed form, UDC-CMG. These results suggest the usefulness of UDC-CMG-PV_2 as the pro-drug in calcium gallstone dissolution therapy.
収録刊行物
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- Journal of pharmacobio-dynamics
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Journal of pharmacobio-dynamics 14 (10), 561-566, 1991-10
公益社団法人日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1572824502319546368
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- NII論文ID
- 110003655000
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- NII書誌ID
- AA00704585
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- ISSN
- 0386846X
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- 本文言語コード
- en
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- データソース種別
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- CiNii Articles