首页    期刊浏览 2025年02月25日 星期二
登录注册

文章基本信息

  • 标题:In Vitro Cytotoxicity of cis[((1R, 2R)-1, 2-Cyclohexanediamine-N, N')bis(myristato)] platinum(II) Suspended in Lipiodol in Rat Hepatoma AH-109A Cells and Human Tumor Cell Lines
  • 本地全文:下载
  • 作者:Shuichi KISHIMOTO ; Toshihiro NOGUCHI ; Takashi YAMAOKA
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2000
  • 卷号:23
  • 期号:4
  • 页码:487-491
  • DOI:10.1248/bpb.23.487
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:SM-11355, cis[((1R, 2R)-1, 2-Cyclohexanediamine-N, N')bis(myristato)] platinum(II), is a lipophilic platinum complex.SM-11355 suspended in Lipiodol (SM-11355/Lipiodol) was shown to have antitumor activity against hepatic tumors after intra-hepatic arterial administration in animal models. In this study, the in vitro growth inhibitory activities of SM-11355 and ciSplatin (CDDP) following 7-d drug exposure were examined using rat ascite hepatoma AH-109A cells and various human tumor cell lines. In monolayer or suSpension cell cultures, SM-11355 did not inhibit the cell growth, whereas SM-11355/Lipiodol had dose-dependent growth inhibitory activities, as did CDDP suspended in Lipiodol (CdDP/Lipiodol). This was also the case in the colony formation assay in agarose gel. CDDP/Lipiodol released platinum compound into the culture medium rapidly, whereas SM-11355/Lipiodol released it slowly but constantly for 7 d. Furthermore, a significant amount of platinum was detected in the cells treated with CDDP/Lipiodol and SM-11355/Lipiodol. These results suggest that Lipiodol plays an important role in the in vitro cytotoxicity of SM-11355, and certain platinum compounds released from SM-11355/Lipiodol have growth inhibitory effects on these cells.
  • 关键词:lipophilic platinum;Lipiodol;hepatocellular caricinoma;cisplatin (CDDP);sustained release;cytotoxicity
国家哲学社会科学文献中心版权所有