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  1. 原著論文

Multifunctional Traceable Liposomes with Temperature-Triggered Drug Release and Neovasculature-Targeting Properties for Improved Cancer Chemotherapy

https://repo.qst.go.jp/records/84603
https://repo.qst.go.jp/records/84603
78d69775-2006-4f63-bca1-eb3d72a2da12
Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-11-13
タイトル
タイトル Multifunctional Traceable Liposomes with Temperature-Triggered Drug Release and Neovasculature-Targeting Properties for Improved Cancer Chemotherapy
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 Yuba, Eiji

× Yuba, Eiji

WEKO 1021160

Yuba, Eiji

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Takashima, Munenobu

× Takashima, Munenobu

WEKO 1021161

Takashima, Munenobu

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Hayashi, Takaaki

× Hayashi, Takaaki

WEKO 1021162

Hayashi, Takaaki

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Kokuryo, Daisuke

× Kokuryo, Daisuke

WEKO 1021163

Kokuryo, Daisuke

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Ichio, Aoki

× Ichio, Aoki

WEKO 1021164

Ichio, Aoki

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Harada, Atsushi

× Harada, Atsushi

WEKO 1021165

Harada, Atsushi

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Aoshima, Sadahito

× Aoshima, Sadahito

WEKO 1021166

Aoshima, Sadahito

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Maheswari Krishnan, Uma

× Maheswari Krishnan, Uma

WEKO 1021167

Maheswari Krishnan, Uma

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Kono, Kenji

× Kono, Kenji

WEKO 1021168

Kono, Kenji

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Ichio, Aoki

× Ichio, Aoki

WEKO 1021169

en Ichio, Aoki

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抄録
内容記述タイプ Abstract
内容記述 Poor distribution of nanocarriers at the tumor site and insufficient drug penetration into the tissue are major challenges in the development of effective and safe cancer therapy. Here, we aim to enhance the therapeutic effect of liposomes by accumulating doxorubicin-loaded liposomes at high concentrations in and around the tumor, followed by heat-triggered drug release to facilitate low-molecular-weight drug penetration throughout the tumor. A cyclic RGD peptide (cRGD) was incorporated into liposomes decorated with a thermosensitive polymer that allowed precise tuning of drug release temperature (i.e., Polymer-lip) to develop a targeted thermosensitive liposome (cRGD-Polymer-lip). Compared with conventional thermosensitive liposomes, cRGD-Polymer-lip enhanced the binding of liposomes to endothelial cells, leading to their accumulation at the tumor site upon intravenous administration in tumor-bearing mice. Drug release triggered by local heating strongly inhibited tumor growth. Notably, tumor remission was achieved via multiple administrations of cRGD-Polymer-lip and heat treatments. Thus, combining the advantages of tumor neovascular targeting and heat-triggered drug release, these liposomes offer high potential for minimally invasive and effective cancer chemotherapy.
書誌情報 Molecular Pharmaceutics

巻 18, 号 9, p. 3342-3351, 発行日 2021-09
出版者
出版者 ACS
ISSN
収録物識別子タイプ ISSN
収録物識別子 1543-8384
DOI
識別子タイプ DOI
関連識別子 10.1021/acs.molpharmaceut.1c00263
関連サイト
識別子タイプ URI
関連識別子 https://pubs.acs.org/doi/10.1021/acs.molpharmaceut.1c00263
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