Synthesis and antitumor activity evaluations of albumin-binding prodrugs of CC-1065 analog |
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Authors: | Wang Yuqiang Jiang Jie Jiang Xiaojian Cai Shaohui Han Hai Li Lianfa Tian Zhiming Jiang Wei Zhang Zaijun Xiao Ying Wright Susan C Larrick James W |
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Affiliation: | Institute of New Drug Research, Jinan University College of Pharmacy, Guangzhou 510632, China. yqwangphd@yahoo.com |
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Abstract: | An albumin-binding prodrug of the extremely potent CC-1065 analog, (+)-FDI-CBI, has been synthesized. This analog, (+)-FDI-CBIM, formed an albumin conjugate when added to human albumin in vitro. A greater amount (>3-fold) of the prodrug can be administered to animals compared to the free drug. The prodrug had significantly improved antitumor efficacy compared to the free drug in animal models using syngeneic animal tumors and human ovarian xenografted tumor cells. Antitumor drug delivery by in situ formation of drug-albumin conjugate is a promising strategy to improve antitumor efficacy. |
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