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  1. 原著論文

Delivery of size-controlled long-circulating polymersomes in solid tumours, visualized by quantum dots and optical imaging in vivo

https://repo.qst.go.jp/records/47261
https://repo.qst.go.jp/records/47261
51731e36-b689-4dde-9935-5317aaf30d29
Item type 学術雑誌論文 / Journal Article(1)
公開日 2015-08-19
タイトル
タイトル Delivery of size-controlled long-circulating polymersomes in solid tumours, visualized by quantum dots and optical imaging in vivo
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 Bakalova-Zheleva, Rumiana

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WEKO 472684

Bakalova-Zheleva, Rumiana

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Lazarova, Desislava

× Lazarova, Desislava

WEKO 472685

Lazarova, Desislava

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Pancheva, Nikolova-Lefterova Biliana

× Pancheva, Nikolova-Lefterova Biliana

WEKO 472686

Pancheva, Nikolova-Lefterova Biliana

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Atanasova, Severina

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WEKO 472687

Atanasova, Severina

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Zlateva, Genoveva

× Zlateva, Genoveva

WEKO 472688

Zlateva, Genoveva

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Zhelev, Zhivko

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WEKO 472689

Zhelev, Zhivko

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Aoki, Ichio

× Aoki, Ichio

WEKO 472690

Aoki, Ichio

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バカロバ ルミアナ

× バカロバ ルミアナ

WEKO 472691

en バカロバ ルミアナ

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ラザロヴァ デシスラヴァ

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WEKO 472692

en ラザロヴァ デシスラヴァ

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ニコロヴァレフタロヴ� .咼螢▲福�

× ニコロヴァレフタロヴ� .咼螢▲福�

WEKO 472693

en ニコロヴァレフタロヴ� .咼螢▲福�

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アタナソヴァ セヴァリナ

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WEKO 472694

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Zhelev Zhivko

× Zhelev Zhivko

WEKO 472695

en Zhelev Zhivko

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青木 伊知男

× 青木 伊知男

WEKO 472696

en 青木 伊知男

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抄録
内容記述タイプ Abstract
内容記述 The present study was designed to investigate whether poly-ion complex hollow vesicles (polymersomes), based on chemically modified chitosan, are appropriate for passive tumour targeting in the context of their application as drug carriers. The experiments were performed on colon cancer-grafted mice. The mice were subjected to anaesthesia and injected intravenously with water-soluble nanoparticles: (1) QD705-labelled polymersomes (average size ∼120 nm; size distribution ∼10%) or (2) native QD705. The optical imaging was carried out on Maestro EX 2.10 In Vivo Imaging System (excitation filter 435–480 nm; emission filter 700 nm, longpass). In the case of QD705, the fluorescence appeared in the tumour area within 1 min after injection and disappeared completely within 60 min. A strong fluorescent signal was detected in the liver on the 30th minute. The visualization of tumour using QD705 was based only on angiogenesis. In the case of QD705-labelled polymersomes, the fluorescence appeared in the tumour area immediately after injection with excellent visualization of blood vessels in the whole body. A strong fluorescent signal was detected in the tumour area within 16 hours. This indicated that QD705-labelled polymersomes were delivered predominantly into the tumour due to their long circulation in the bloodstream and enhanced permeability and retention effect. A very weak fluorescent signal was found in the liver area. The data suggest that size-controlled long-circulating polymersomes are very promising carriers for drug delivery in solid tumours, including delivery of small nanoparticles and contrast substances.
書誌情報 Biotechnology & Biotechnological Equipment

巻 29, 号 1, p. 175-180, 発行日 2014-11
出版者
出版者 Taylor & Francis
ISSN
収録物識別子タイプ ISSN
収録物識別子 1310-2818
DOI
識別子タイプ DOI
関連識別子 DOI: 10.1080/13102818.2014.984894
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