甲磺酸
无水的
溶解度
工艺工程
化学
过程开发
水溶液
药品
盐(化学)
药理学
组合化学
医学
有机化学
工程类
作者
Bo Mei,Linrong Zhu,Yushen Guo,Tao Wu,Pingda Ren,Xiaohu Deng
标识
DOI:10.1021/acs.oprd.1c00113
摘要
KO-947 is a potent, selective extracellular signal-regulated kinases (ERK) inhibitor that was investigated in the clinic for the treatment of various solid tumors. KO-947 free base, form E, was originally recommended out of 10 identified crystalline forms for the development of an oral solid dosage product. Change of clinical need shifted the focus to aqueous solubility enhancement through salt formation. Mesylate salt demonstrated remarkably increased aqueous solubility and also profound polymorphism. Anhydrous form III was initially recommended but later dropped, primarily due to the manufacturing difficulties. In the end, form IX was discovered through close collaboration between preformulation and process scientists. An elaborate manufacturing process was then devised to successfully produce mesylate salt, form IX in kilogram scale supplied for the clinical use.
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