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RADIOLYSIS OF C-11-Ro 15-4513 IN AN AQUEOUS SOLUTION

https://repo.qst.go.jp/records/68555
https://repo.qst.go.jp/records/68555
c81b71b5-3fcd-43b2-bd8b-1a0a8a0f98ed
Item type 会議発表用資料 / Presentation(1)
公開日 2006-06-30
タイトル
タイトル RADIOLYSIS OF C-11-Ro 15-4513 IN AN AQUEOUS SOLUTION
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 Fukumura, Toshimitsu

× Fukumura, Toshimitsu

WEKO 672837

Fukumura, Toshimitsu

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Akaike, Shihoko

× Akaike, Shihoko

WEKO 672838

Akaike, Shihoko

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Yoshida, Yuichirou

× Yoshida, Yuichirou

WEKO 672839

Yoshida, Yuichirou

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Suzuki, Kazutoshi

× Suzuki, Kazutoshi

WEKO 672840

Suzuki, Kazutoshi

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福村 利光

× 福村 利光

WEKO 672841

en 福村 利光

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吉田 勇一郎

× 吉田 勇一郎

WEKO 672842

en 吉田 勇一郎

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鈴木 和年

× 鈴木 和年

WEKO 672843

en 鈴木 和年

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抄録
内容記述タイプ Abstract
内容記述 AIMS: Recent development of PET radiopharmaceutical production technique has made it possible to prepare C-11 labelled compounds with extremely high specific activity (more than 10 Ci/_mol). C-11-Ro 15-4513 has been used for benzodiazepine receptor imaging and recently is needed to be labelled with such an extremely high specific activity to image high affinity binding site. However, large amount of radioactivity and extremely high specific activity might cause the possibility of radiolysis. Therefore we investigated the mechanism of radiolysis of C-11-Ro 15-4513 to suppress the decomposition of C-11-Ro 15-4513 in aqueous solution.
METHODS: C-11-Ro 15 4513 was prepared by C-11 methylation of desmethy precursor with C-11-CH3I. After purification with HPLC system (column: C-18, mobile phase: 40% CH3CN), C-11-Ro 15-4513 fraction was evaporated to dryness and C-11-Ro 15-4513 was dissolved in pure H2O. C-11-Ro 15-4513 solution was allowed to stand to give degradation product. And the degradation products were estimeted with decomposed samples of authentic Ro 15-4513 solution by Co-60 or UV photolysis by comparing with those retention time. Chemical structure of degrdation products was estimeted with LC/MS. Effect of additives (MeOH, EtOH, HCOONH4, NaNO3, etc) on radiolysis of Ro 15-4513 was also examined.
RESULTS: C-11-Ro 15-4513 solution underwent radiolysis to give one major and another minor radioactive degradation product. The major degradation product had same retention time with that of degradation product with Co-60. And minor degradation product was corresponded to degradation product by UV photolysis. The structure of degradation product by radiolysis and photolysis was estimated that azido group in Ro 15-4513 was displaced by amine and hydroxylamine group respectively from mass spectra. From the examination of radiolysis with Co-60 and radiolysis of C-11-Ro 15-4513 in the presence of additives, addition of selective hydroxyradical scavenger such as MeOH and EtOH accelerated the radiolysis of Ro 15-4513. In contrast the radiolysis was effectively suppressed by addition of selective hydrated electron scavenger (e.g. NaNO3), suggesting a possibility that hydrated electron would play important role to the radiolysis of C-11-Ro 15-4513.
CONCLUSION: From this investigation addition of selective hydroxyl radical scavenger accelerated the radiolysis of C-11-Ro 15-4513, in contrast the radiolysis was suppressed perfectly by addition of selective hydrated electron scavenger. These results would suggest the participation of hydrated electron to the radiolysis of Ro-15-4513.
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 Ninth International Worksshop on Targetry and TargetChemistry
発表年月日
日付 2002-05-30
日付タイプ Issued
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