ログイン
言語:

WEKO3

  • トップ
  • ランキング
To
lat lon distance
To

Field does not validate



インデックスリンク

インデックスツリー

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. 原著論文

Development of Antibody–Drug Conjugates Using DDS and Molecular Imaging

https://repo.qst.go.jp/records/48406
https://repo.qst.go.jp/records/48406
f1dbf7bc-8bcc-40c7-9643-0ca46210d1ea
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-12-06
タイトル
タイトル Development of Antibody–Drug Conjugates Using DDS and Molecular Imaging
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 Yasunaga, Masahiro

× Yasunaga, Masahiro

WEKO 486558

Yasunaga, Masahiro

Search repository
Manabe, Shino

× Manabe, Shino

WEKO 486559

Manabe, Shino

Search repository
Tsuji, Atsushi

× Tsuji, Atsushi

WEKO 486560

Tsuji, Atsushi

Search repository
Tsuneo, Saga

× Tsuneo, Saga

WEKO 486561

Tsuneo, Saga

Search repository
辻 厚至

× 辻 厚至

WEKO 486562

en 辻 厚至

Search repository
抄録
内容記述タイプ Abstract
内容記述 Antibody-drug conjugate (ADC), as a next generation of antibody therapeutics, is a combination of an antibody and a drug connected via a specialized linker. ADC has four action steps: systemic circulation, the enhanced permeability and retention (EPR) effect, penetration within the tumor tissue, and action on cells, such as through drug delivery system (DDS) drugs. An antibody with a size of about 10 nm has the same capacity for passive targeting as some DDS carriers, depending on the EPR effect. In addition, some antibodies are capable of active targeting. A linker is stable in the bloodstream but should release drugs efficiently in the tumor cells or their microenvironment. Thus, the linker technology is actually a typical controlled release technology in DDS. Here, we focused on molecular imaging. Fluorescent and positron emission tomography (PET) imaging is useful for the visualization and evaluation of antibody delivery in terms of passive and active targeting in the systemic circulation and in tumors. To evaluate the controlled release of the ADC in the targeted area, a mass spectrometry imaging (MSI) with a mass microscope, to visualize the drug released from ADC, was used. As a result, we succeeded in confirming the significant anti-tumor activity of anti-fibrin, or anti-tissue factor-ADC, in preclinical settings by using DDS and molecular imaging.
書誌情報 Bioengineering

巻 4, 号 3, p. 78-1-78-13, 発行日 2017-09
出版者
出版者 Multidisciplinary Digital Publishing Institut
PubMed番号
識別子タイプ PMID
関連識別子 28952557
DOI
識別子タイプ DOI
関連識別子 10.3390/bioengineering4030078
関連サイト
識別子タイプ URI
関連識別子 https://www.ncbi.nlm.nih.gov/pubmed/?term=PMC5615324
関連名称 https://www.ncbi.nlm.nih.gov/pubmed/?term=PMC5615324
戻る
0
views
See details
Views

Versions

Ver.1 2023-05-15 23:28:28.528130
Show All versions

Share

Mendeley Twitter Facebook Print Addthis

Cite as

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX

Confirm


Powered by WEKO3


Powered by WEKO3