書誌事項
- タイトル別名
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- Blood concentration of cevimeline hydrochloride hydrate after oral rinsing
- セビメリン エンサンエン スイワブツ ニ ヨル コウコウ リンスホウ ゴ ノ ケッチュウ ノウド ノ スイイ
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説明
Cevimeline hydrochloride hydrate (cevimeline) is used in the treatment of xerostomia associated with Sjogren's syndrome. However, this medication has muscarinic agonist activity and is associated with several adverse effects, including nausea, vomiting, and diarrhea. Oral rinsing with cevimeline is recommended to avoid these adverse effects, but cevimeline blood concentration after rinsing has not been thoroughly investigated. This study measured blood cevimeline concentration after oral rinsing at a concentration of 30 mg in 50 ml of water and determined that the maximum plasma concentration of 4.04 ± 1.10 ng/ml occurred two hours later, which is longer than the time to maximum concentration after an oral administration of 30 mg. Furthermore, the maximum concentration after rinsing was 5.5% of the maximum concentration after oral administration, and the half-life after rinsing was 6 hours, which is longer than the half-life after oral administration.
収録刊行物
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- 日本口腔科学会雑誌
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日本口腔科学会雑誌 62 (1), 1-4, 2013
特定非営利活動法人 日本口腔科学会
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詳細情報 詳細情報について
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- CRID
- 1390282681412723712
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- NII論文ID
- 130004555777
- 40019657415
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- NII書誌ID
- AN00189050
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- ISSN
- 21850461
- 00290297
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- NDL書誌ID
- 024576065
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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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- JaLC
- NDLサーチ
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可