論文

査読有り
2013年7月

Tumor growth suppression by gadolinium-neutron capture therapy using gadolinium-entrapped liposome as gadolinium delivery agent

Biomedicine and Pharmacotherapy
  • Novriana Dewi
  • Hironobu Yanagie
  • Haito Zhu
  • Kazuyuki Demachi
  • Atsuko Shinohara
  • Kazuhito Yokoyama
  • Masaki Sekino
  • Yuriko Sakurai
  • Yasuyuki Morishita
  • Naoko Iyomoto
  • Takeshi Nagasaki
  • Yukichi Horiguchi
  • Yukio Nagasaki
  • Jun Nakajima
  • Minoru Ono
  • Kazuhiro Kakimi
  • Hiroyuki Takahashi
  • 全て表示

67
6
開始ページ
451
終了ページ
457
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.biopha.2012.11.010

Neutron capture therapy (NCT) is a promising non-invasive cancer therapy approach and some recent NCT research has focused on using compounds containing gadolinium as an alternative to currently used boron-10 considering several advantages that gadolinium offers compared to those of boron. In this study, we evaluated gadolinium-entrapped liposome compound as neutron capture therapy agent by in vivo experiment on colon-26 tumor-bearing mice. Gadolinium compound were injected intravenously via tail vein and allowed to accumulate into tumor site. Tumor samples were taken for quantitative analysis by ICP-MS at 2, 12, and 24h after gadolinium compound injection. Highest gadolinium concentration was observed at about 2h after gadolinium compound injection with an average of 40.3μg/g of wet tumor tissue. We performed neutron irradiation at JRR-4 reactor facility of Japan Atomic Energy Research Institute in Tokaimura with average neutron fluence of 2×1012 n/cm2. The experimental results showed that the tumor growth suppression of gadolinium-injected irradiated group was revealed until about four times higher compared to the control group, and no significant weight loss were observed after treatment suggesting low systemic toxicity of this compound. The gadolinium-entrapped liposome will become one of the candidates for Gd delivery system on NCT. © 2013 Elsevier Masson SAS.

リンク情報
DOI
https://doi.org/10.1016/j.biopha.2012.11.010
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/23743325
ID情報
  • DOI : 10.1016/j.biopha.2012.11.010
  • ISSN : 0753-3322
  • ISSN : 1950-6007
  • PubMed ID : 23743325
  • SCOPUS ID : 84880930693

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