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  1. 原著論文

Feedback-controlled bolus plus infusion (FC-B/I) method for quantitative drug assessment in living brain with PET

https://repo.qst.go.jp/records/46393
https://repo.qst.go.jp/records/46393
4ab4f61b-87f3-4962-8eab-d3a6721cc7ce
Item type 学術雑誌論文 / Journal Article(1)
公開日 2012-09-19
タイトル
タイトル Feedback-controlled bolus plus infusion (FC-B/I) method for quantitative drug assessment in living brain with PET
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Kimura, Yuichi

× Kimura, Yuichi

WEKO 462166

Kimura, Yuichi

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et.al

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et.al

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木村 裕一

× 木村 裕一

WEKO 462168

en 木村 裕一

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抄録
内容記述タイプ Abstract
内容記述 We have developed a feedback-controlled bolus plus infusion (FC-B/I) method for monitoring the interaction between positron
emission tomography (PET) ligands and their specific target molecules with PET. The usefulness of the FC-B/I method was evaluated
by the direct interaction between [11C]raclopride, a dopamine D2 receptor (D2R) ligand, and cold raclopride (10 and 100 mg/kg) in
the brains of conscious monkeys. The present results demonstrated that the FC-B/I method could achieve the equilibrium state of
[11C]raclopride in the striatum of monkey brain, and also that the cold raclopride-induced reduction of [11C]raclopride binding to
D2R was observed in a dose-dependent manner. Good correlations of distribution volume ratio of the striatum to cerebellum
between the conventional bolus plus infusion (B/I) method and the FC-B/I method as well as between the conventional bolus
injection method and the FC-B/I method were observed. These results indicated that the system could be a useful tool for the
evaluation of interaction between drug candidates and their target molecules like enzymes, receptors, and transporters by using of
their specific PET ligands.
書誌情報 Journal of Cerebral Blood Flow and Metabolism

巻 33, 号 1, p. 85-90, 発行日 2012-09
ISSN
収録物識別子タイプ ISSN
収録物識別子 0271-678X
DOI
識別子タイプ DOI
関連識別子 10.1038/jcbfm.2012.134
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