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  1. 原著論文

Enhanced MRI-Guided Gadolinium (III) Neutron Capture Therapyby Polymeric Nanocarriers Promoting Tumor Accumulation andIntracellular Delivery

https://repo.qst.go.jp/records/80043
https://repo.qst.go.jp/records/80043
a3017159-3302-47f7-b067-773dad074aa1
Item type 学術雑誌論文 / Journal Article(1)
公開日 2020-06-09
タイトル
タイトル Enhanced MRI-Guided Gadolinium (III) Neutron Capture Therapyby Polymeric Nanocarriers Promoting Tumor Accumulation andIntracellular Delivery
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 Qin, Changyuan

× Qin, Changyuan

WEKO 929871

Qin, Changyuan

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Hou, Xuan

× Hou, Xuan

WEKO 929872

Hou, Xuan

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Khan, Thahomina

× Khan, Thahomina

WEKO 929873

Khan, Thahomina

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Nitta, Nobuhiro

× Nitta, Nobuhiro

WEKO 929874

Nitta, Nobuhiro

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Yanagawa, Masashi

× Yanagawa, Masashi

WEKO 929875

Yanagawa, Masashi

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Sakurai , Yuriko

× Sakurai , Yuriko

WEKO 929876

Sakurai , Yuriko

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Suzuki, Minoru

× Suzuki, Minoru

WEKO 929877

Suzuki, Minoru

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Shin‐Ichiro, Masunaga

× Shin‐Ichiro, Masunaga

WEKO 929878

Shin‐Ichiro, Masunaga

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Tanaka, Hiroki

× Tanaka, Hiroki

WEKO 929879

Tanaka, Hiroki

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Sakurai, Yoshinori

× Sakurai, Yoshinori

WEKO 929880

Sakurai, Yoshinori

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Takahashi, Hiroyuki

× Takahashi, Hiroyuki

WEKO 929881

Takahashi, Hiroyuki

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Aoki, Ichio

× Aoki, Ichio

WEKO 929882

Aoki, Ichio

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Yanagie, Hironobu

× Yanagie, Hironobu

WEKO 929883

Yanagie, Hironobu

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Nobuhiro, Nitta

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WEKO 929884

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Ichio, Aoki

× Ichio, Aoki

WEKO 929885

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抄録
内容記述タイプ Abstract
内容記述 Gadolinium(III) (Gd(III)) chelates are promising compounds for developing MRI‐guided neutron capture therapies (NCT). However, despite their success as MRI contrast agents (CAs), current Gd(III) chelates do not present appropriate accumulation in tumors for effective NCT. To overcome this limitation, we developed a series of biocompatible polymeric nanocarriers conjugating Gd(III)‐chelates, i. e. Gd‐DOTA, as NCT agents with high MRI sensitivity and tumor delivery. These polymers were based on poly(aspartic acid) (P(Asp)) and were modified with poly(ethylene glycol) (PEG) chains having different molecular weight (Mw) for controlling stability and pharmacokinetics. The T1 relaxivity of the Gd‐DOTA conjugated polymers increased 2‐fold compared to that of clinically used Gd(III) CAs. In vivo, the PEG‐modified polymers promoted the accumulation in tumor tissues, enhancing the MRI contrast of tumors. After neutron irradiation, the nanocarriers effectively suppressed the tumor growth, particularly the PEG‐P(Asp‐Gd‐DOTA) with shorter PEG chain, which promoted higher intracellular delivery, supporting their potential as NCT agents.
書誌情報 ChemNanoMat

巻 6, 号 3, p. 412-419, 発行日 2020-03
ISSN
収録物識別子タイプ ISSN
収録物識別子 2199-692X
DOI
識別子タイプ DOI
関連識別子 10.1002/cnma.201900730
関連サイト
識別子タイプ URI
関連識別子 https://onlinelibrary.wiley.com/doi/full/10.1002/cnma.201900730
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