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  1. 学術雑誌論文
  2. 各雑誌掲載論文

Development of tissue factor-targeted liposomes for effective drug delivery to stroma-rich tumors

http://hdl.handle.net/10271/00003896
http://hdl.handle.net/10271/00003896
07dadbe2-39aa-4baf-99a7-c704a69c7f74
名前 / ファイル ライセンス アクション
JCR-323-519.pdf JCR-323-519.pdf (9.7 MB)
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Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-10-05
タイトル
タイトル Development of tissue factor-targeted liposomes for effective drug delivery to stroma-rich tumors
言語 en
言語
言語 eng
キーワード
主題 Antibody
キーワード
主題 liposome
キーワード
主題 pancreatic tumor
キーワード
主題 targeting
キーワード
主題 tissue factor
キーワード
主題 tumor stroma
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
著者 Shimizu, Kosuke

× Shimizu, Kosuke

en Shimizu, Kosuke

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Takeuchi, Yoshihito

× Takeuchi, Yoshihito

en Takeuchi, Yoshihito

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Otsuka, Kazuma

× Otsuka, Kazuma

en Otsuka, Kazuma

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Mori, Tomoya

× Mori, Tomoya

en Mori, Tomoya

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Narita, Yudai

× Narita, Yudai

en Narita, Yudai

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Takasugi, Shohei

× Takasugi, Shohei

en Takasugi, Shohei

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Magata, Yasuhiro

× Magata, Yasuhiro

en Magata, Yasuhiro

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Matsumura, Yasuhiro

× Matsumura, Yasuhiro

en Matsumura, Yasuhiro

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Oku, Naoto

× Oku, Naoto

en Oku, Naoto

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書誌情報 en : Journal of Controlled Release

巻 323, p. 519-529, 発行日 2020-07-10
出版者
出版者 Elsevier
言語 en
権利
権利情報 Copyright 2020 Elsevier. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
権利
権利情報 This is the accepted manuscript version. The formal published version is available at "https://doi.org/10.1016/j.jconrel.2020.04.043".
抄録
内容記述タイプ Abstract
内容記述 Tissue factor (TF), which is well known as a trigger molecule of extrinsic coagulation, is found in not only tumor cells but also in stromal cells in tumor tissues. Thus, TF is a candidate molecule to potentially enable targeting of both tumor cells and stromal cells for anti-cancer drug delivery. Herein, we prepared liposomes conjugated with the Fab’ fragment of anti-TF antibody (TF Ab- Lip) and evaluated the capability for drug delivery to stroma-rich tumors for realizing a whole tumor tissue-targetable strategy. When the targetability of TF Ab-Lip to TF-expressing KLN205 squamous tumor cells and NIH3T3 fibroblast cells were examined, TF Ab-Lip was significantly taken up into both cells compared with non-targeted liposomes. Corresponding to this result, doxorubicin-encapsulated TF Ab-Lip (TF Ab-LipDOX) showed potent cytotoxicity against KLN205 cells. In vivo experiments using KLN205 solid tumor-bearing mice indicated that TF Ab-Lip became highly accumulated and distributed widely in not only the tumor cell region but also in the stromal one in the tumor. Treatment with TF Ab-LipDOX significantly suppressed the growth of KLN205 solid tumors. Furthermore, TF Ab-Lip targetable both mouse and human TF (mhTF Ab-Lip) became distributed throughout stroma-rich human pancreatic BxPC3 tumors and the treatment of the BxPC3 tumor-bearing mice with mhTF Ab-LipDOX showed highest tumor suppressive effect. These data suggest that TF Ab-Lip could achieve effective accumulation for stroma-rich tumor treatment.
注記
内容記述 <参照>出版社サイト:https://doi.org/10.1016/j.jconrel.2020.04.043
ISSN
収録物識別子タイプ PISSN
収録物識別子 0168-3659
EISSN
収録物識別子タイプ EISSN
収録物識別子 1873-4995
PubMed番号
関連タイプ isVersionOf
識別子タイプ PMID
関連識別子 32360306
出版社DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1016/j.jconrel.2020.04.043
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
出版社版
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1016/j.jconrel.2020.04.043
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