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  1. K-1. 新学術創成研究機構
  2. k-1 10. 学術雑誌掲載論文
  3. 1. 査読済論文

Evaluation of radioiodinated vesamicol analogs for sigma receptor imaging in tumor and radionuclide receptor therapy

https://doi.org/10.24517/00015278
https://doi.org/10.24517/00015278
dec07426-7ae4-465e-8330-2ac7ec8a08df
名前 / ファイル ライセンス アクション
ME-PR-OGAWA-K-2188.pdf ME-PR-OGAWA-K-2188.pdf (231.6 kB)
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Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-04
タイトル
タイトル Evaluation of radioiodinated vesamicol analogs for sigma receptor imaging in tumor and radionuclide receptor therapy
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
ID登録
ID登録 10.24517/00015278
ID登録タイプ JaLC
著者 Ogawa, Kazuma

× Ogawa, Kazuma

WEKO 87
e-Rad 30347471
金沢大学研究者情報 30347471
研究者番号 30347471

Ogawa, Kazuma

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Shiba, Kazuhiro

× Shiba, Kazuhiro

WEKO 43
e-Rad 40143929
金沢大学研究者情報 40143929
研究者番号 40143929

Shiba, Kazuhiro

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Akhter, Nasima

× Akhter, Nasima

WEKO 27695

Akhter, Nasima

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Yoshimoto, Mitsuyoshi

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WEKO 27696
e-Rad 00345638
研究者番号 00345638

Yoshimoto, Mitsuyoshi

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Washiyama, Kohshin

× Washiyama, Kohshin

WEKO 139
e-Rad 80313675
金沢大学研究者情報 80313675
研究者番号 80313675

Washiyama, Kohshin

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Kinuya, Seigo

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WEKO 115
e-Rad 20281024
金沢大学研究者情報 20281024
研究者番号 20281024

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Kawai, Keiichi

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WEKO 40
e-Rad 30204663
金沢大学研究者情報 30204663
研究者番号 30204663

Kawai, Keiichi

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Mori, Hirofumi

× Mori, Hirofumi

WEKO 20737
e-Rad 90019604
研究者番号 90019604

Mori, Hirofumi

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著者別表示 小川, 数馬

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小川, 数馬

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柴, 和弘

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柴, 和弘

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吉本, 光喜

× 吉本, 光喜

吉本, 光喜

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鷲山, 幸信

× 鷲山, 幸信

鷲山, 幸信

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絹谷, 清剛

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絹谷, 清剛

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川井, 恵一

× 川井, 恵一

川井, 恵一

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提供者所属
内容記述タイプ Other
内容記述 金沢大学新学術創成研究機構 / 金沢大学医薬保健研究域薬学系
書誌情報 Cancer Science

巻 100, 号 11, p. 2188-2192, 発行日 2009-11-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 1347-9032
NCID
収録物識別子タイプ NCID
収録物識別子 AA11808050
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1111/j.1349-7006.2009.01279.x
出版者
出版者 Japanese Cancer Association = 日本癌学会
抄録
内容記述タイプ Abstract
内容記述 It has been reported that sigma receptors are highly expressed in a variety of human tumors. In this study, we selected (+)-2-[4-(4-iodophenyl)piperidino] cyclohexanol [(+)-pIV] as a sigma receptor ligand and evaluated the potential of radioiodinated (+)-pIV for tumor imaging and therapy. (+)-[125/131I]pIV was prepared by an iododestannylation reaction under no-carrier-added conditions with radiochemical purity over 99% after HPLC purification. Biodistribution experiments were performed by the intravenous injection of (+)-[125I]pIV into mice bearing human prostate tumors (DU-145). Blocking studies were performed by intravenous injection of (+)-[125I]pIV mixed with an excess amount of unlabeled sigma ligand into DU-145 tumor-bearing mice. For therapeutic study, (+)-[131I]pIV was injected at a dose of 7.4 MBq followed by measurement of the tumor size. In biodistribution experiments, (+)-[125I]pIV showed high uptake and long residence in the tumor. High tumor to blood and muscle ratios were achieved because the radioactivity levels of blood and muscle were low. However, the accumulations of radioactivity in non-target tissues, such as liver and kidney, were high. The radioactivity in the non-target tissues slowly decreased over time. Co-injection of (+)-[125I]pIV with an excess amount of unlabeled sigma ligand resulted in a significant decrease in the tumor/blood ratio, indicating sigma receptor-mediated tumor uptake. In therapeutic study, tumor growth in mice treated with (+)-[131I]pIV was significantly inhibited compared to that of an untreated group. These results indicate that radioiodinated (+)-pIV has a high potential for sigma receptor imaging in tumor and radionuclide receptor therapy. (Cancer Sci 2009). © 2009 Japanese Cancer Association.
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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