Antitumor activities and pharmacokinetics of silatecans DB-67 and DB-91

Teng Kuang Yeh, Chien Ming Li, Ching Ping Chen, Jiuun Jye Chuu, Chen Lung Huang, Hsin Sheng Wang, Chien Chang Shen, Tien Yi Lee, Chi Yen Chang, Chung Ming Chang, Yu Sheng Chao, Chin Tarng Lin, Jang Yang Chang, Chiung Tong Chen

研究成果: Article

11 引文 斯高帕斯(Scopus)

摘要

DB-67 and its lactone homolog DB-91 are derivatives of topoisomerase I inhibitor camptothecin (CPT) with silyl moiety, which may exhibit a slower inactivation process by changed kinetics of protein binding and/or hydrolysis of its lactone ring and result in increased antitumor activity and decreased toxicity. Pharmacokinetic properties and antitumor activities of the two silatecans were studied and compared. The lactone ring of DB-91 is more stable than those of all the other CPT derivatives in mouse plasma. Both silatecans were metabolized faster than CPT in mouse and human liver microsomes. Pharmacokinetic study revealed a plasma elimination half-life (t1/2) of 33 and 94 min for DB-67 and DB-91, respectively; similar systemic exposure in plasma between DB-67 and DB-91; and similar volume of distribution at the steady state between DB-67 and DB-91, approximately 15-fold smaller than that of CPT. While DB-91 showed limited activities, DB-67 exhibited activities against the growth of in vivo-like histocultured human tumors and s.c. xenografted human tumors in nude mice. In conclusion, DB-67 is more effective, compared to DB-91, against human tumor growth in in vitro, in vivo-like and in vivo systems. Further pre-clinical and clinical investigations of DB-67 are warranted.

原文English
頁(從 - 到)108-115
頁數8
期刊Pharmacological Research
61
發行號2
DOIs
出版狀態Published - 2010 二月 1

    指紋

All Science Journal Classification (ASJC) codes

  • Pharmacology

引用此

Yeh, T. K., Li, C. M., Chen, C. P., Chuu, J. J., Huang, C. L., Wang, H. S., Shen, C. C., Lee, T. Y., Chang, C. Y., Chang, C. M., Chao, Y. S., Lin, C. T., Chang, J. Y., & Chen, C. T. (2010). Antitumor activities and pharmacokinetics of silatecans DB-67 and DB-91. Pharmacological Research, 61(2), 108-115. https://doi.org/10.1016/j.phrs.2009.07.005