前药
化学
伊立替康
PEG比率
喜树碱
乙二醇
结合
序号38
组合化学
活性代谢物
娴熟的
溶解度
立体化学
生物化学
代谢物
癌症
有机化学
结直肠癌
内科学
数学分析
经济
医学
数学
财务
作者
Hong Zhao,Belen Rubio,Puja Sapra,Dechun Wu,Prasanna Reddy,Prakash Sai,Anthony Martinez,Ying Gao,Yoany Lozanguiez,Clifford Longley,Lee M. Greenberger,Ivan D. Horak
摘要
CPT-11, also known as irinotecan, is a prodrug that is approved for the treatment of advanced colorectal cancer. The active metabolite of CPT-11, SN38 (7-ethyl-10-hydroxy-camptothecin), has 100- to 1000-fold more potent cytotoxic activity in tissue cell culture compared with CPT-11. However, parental administration of SN38 is not possible because of its inherently poor water solubility. It is reported here that a multiarm poly(ethylene glycol) (PEG) backbone linked to four SN38 molecules (PEG-SN38) has been successfully prepared with high drug loading and significantly improved water solubility (400- to 1000-fold increase). Three different protecting strategies have been developed in order to selectively acylate the 20-OH of SN38 to preserve its E-ring in the lactone form (the active form of SN38 with cytotoxic activities) while PEG is still attached. One chemical process has been optimized to make a large quantity of the PEG-SN38 conjugate with a high yield that can be readily adapted for scale-up production. The PEG-SN38 conjugates have shown excellent in vitro anticancer activity, with potency similar to that of native SN38, in a panel of cancer cell lines. The PEG-SN38 conjugates also have demonstrated superior anticancer activity in the MX-1 xenograft mice model compared with CPT-11. Among the four conjugates, PEG-Gly-(20)-SN38 (23) has been selected as the lead candidate for further preclinical development.
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