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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/8460378d69775-2006-4f63-bca1-eb3d72a2da12
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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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× Takashima, Munenobu× Hayashi, Takaaki× Kokuryo, Daisuke× Ichio, Aoki× Harada, Atsushi× Aoshima, Sadahito× Maheswari Krishnan, Uma× Kono, Kenji× 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 |
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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 | |||||
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識別子タイプ | URI | |||||
関連識別子 | https://pubs.acs.org/doi/10.1021/acs.molpharmaceut.1c00263 |