Anticancer efficacy with cisplatin delivery systems

  • Akio Sugitachi
  • , Yusuke Kimura
  • , Tetsuya Itabashi
  • , Miyuki Ikeda
  • , Kazushige Ishida
  • , Hironobu Noda
  • , Teppei Matsuo
  • , Satoshi Nishizuka
  • , Koki Otsuka
  • , Keisuke Koeda
  • , Ayako Sato
  • , Tomoki Takahashi
  • , Go Wakabayashi

Research output: Contribution to journalArticlepeer-review

Abstract

The authors devised two different types of cisplatin (CDDP) delivery systems; namely, System A and System B. The anticancer efficacy with each system was examined using cancer-bearing animals. Seventy-percent deacetylated chitin (DAC-70) was used as the drug carrier in the system. Cancer-bearing animals were prepared by intra-peritoneally (ip) inoculating the MM-46 cancer cells to C3H mice. Each novel system was also ip injected to the cancer-bearing mouse, and then survival time of each animal was recorded to evaluate the anti- cancer efficacy of the system. Both Systems A and B were viscoelastic sol at 25°C and slowly changed to gel at 37°C. Four-week survival rate of each animal treated with the System was as follows: System A 6/10 (60%), System B 10/11 (90.9%), conventional CDDP alone 3/9 (33.3%) and non-treated 0/7 (0%). No signs of recurrence of ascites were encountered in the long-term survived animals treated with System A and B. Our newly devised systems provided a favorable antitumor efficacy in vivo. Now, we will carry out further studies by making a clinically applicable novel conjugated system, DAC-70 and CDDP.

Original languageEnglish
Pages (from-to)2274-2276
Number of pages3
JournalJapanese Journal of Cancer and Chemotherapy
Volume37
Issue number12
Publication statusPublished - 11-2010
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General Medicine

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