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PET imaging and quantification of the effects of succinylated gelatin and/or L-lysine on renal uptake and retention of the novel radiopharmaceutical 64Cu-cyclam-RAFT-c(-RGDfK-)4

https://repo.qst.go.jp/records/71164
https://repo.qst.go.jp/records/71164
50c9dddc-5038-46a6-af5b-ed637db4e882
Item type 会議発表用資料 / Presentation(1)
公開日 2013-06-20
タイトル
タイトル PET imaging and quantification of the effects of succinylated gelatin and/or L-lysine on renal uptake and retention of the novel radiopharmaceutical 64Cu-cyclam-RAFT-c(-RGDfK-)4
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_c94f
資源タイプ conference object
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 Jin, Zhao-Hui

× Jin, Zhao-Hui

WEKO 699600

Jin, Zhao-Hui

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Furukawa, Takako

× Furukawa, Takako

WEKO 699601

Furukawa, Takako

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Sogawa, Chizuru

× Sogawa, Chizuru

WEKO 699602

Sogawa, Chizuru

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Tsuji, Atsushi

× Tsuji, Atsushi

WEKO 699603

Tsuji, Atsushi

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U, Winn Aung

× U, Winn Aung

WEKO 699604

U, Winn Aung

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Coll, Jean-Luc

× Coll, Jean-Luc

WEKO 699605

Coll, Jean-Luc

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 699606

Saga, Tsuneo

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et.al

× et.al

WEKO 699607

et.al

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金 朝暉

× 金 朝暉

WEKO 699608

en 金 朝暉

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古川 高子

× 古川 高子

WEKO 699609

en 古川 高子

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曽川 千鶴

× 曽川 千鶴

WEKO 699610

en 曽川 千鶴

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辻 厚至

× 辻 厚至

WEKO 699611

en 辻 厚至

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U Winn Aung

× U Winn Aung

WEKO 699612

en U Winn Aung

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佐賀 恒夫

× 佐賀 恒夫

WEKO 699613

en 佐賀 恒夫

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抄録
内容記述タイプ Abstract
内容記述 Objective: 64Cu-cyclam-RAFT-c(-RGDfK-)4 (64Cu-RAFTRGD) is a novel tetrameric cyclic RGD peptide probe for PET imaging of tumor angiogenesis via targeting the V3 integrin. Because 64Cu also emits -, it can be used for internal radiotherapy. We studied the effects of a succinylated gelatin-containing plasma expander Gelofusine and L-lysine on the renal uptake and retention of 64Cu-RAFTRGD in tumor-bearing mice, aiming to find measures to lower the risk of nephrotoxicity in internal radiotherapy using 64Cu-RAFTRGD.
Methods: Normal or tumor-bearing mice received injection of 64Cu-RAFTRGD with or without co-injection of Gelofusine, L-lysine, or the both. Biodistribution studies were performed at 3 and 24 h post-injection (p.i.). Dynamic PET scans (5 min/frame) were performed at 0-60 min p.i., followed by static PET scans at 3.5 and 24 h p.i. Radio-TLC was done to analyze the radioactive metabolites in blood, urine, liver, and kidney samples at 1 and 24 h p.i.
Results: Co-injection of Gelofusine significantly reduced the renal uptake and retention of 64Cu-RAFTRGD. Although L-lysine alone had no influence on the renal radioactivity accumulation, it showed the tendency to enhance the inhibitory effect of Gelofusine. The uptake of 64Cu-RAFTRGD in the tumors was not influenced by co-injection of Gelofusine or together with L-lysine. Dynamic PET imaging of mice and metabolic analysis of tissue samples clearly showed that Gelofusine did block the renal reabsorption of 64Cu-RAFTRGD, and did not interfere with the metabolism and excretion pathway of the probe.
Conclusion: Administration of Gelofusine or together with L-lysine is a promising measure for kidney protection in internal radiotherapy using 64Cu-RAFTRGD.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 SNMMI 2013 Annual Meeting
発表年月日
日付 2013-06-12
日付タイプ Issued
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