Fuse Eiichi, Kuwabara Takashi, Sparreboom Alex, Sausville Edward A, Figg William D
PharmD, Clinical Pharmacology Research Core, National Cancer Institute, 9000 Rockville Pike, Bethesda, MD 20892, USA.
J Clin Pharmacol. 2005 Apr;45(4):394-403. doi: 10.1177/0091270005274549.
UCN-01 is a protein kinase inhibitor under development as a novel anticancer drug. The initial pharmacologic features in patients were not predicted from preclinical experiments. The distribution volume and the systemic clearance were much lower than those in experimental animals (mice, rats, and dogs), and the elimination half-life was unusually long (>200 hours). The unbound fraction in human plasma was also much smaller than that in dogs, rats and mice, as was the binding of UCN-01 to human alpha-1 acid glycoprotein much stronger than that to human serum albumin or human gamma-globulin. The association constants for alpha-1 acid glycoprotein and human plasma were approximately 8 x 10(8)(mol/L)(-1), indicating extremely high affinity. In this review article, the authors discuss the pharmacologic features of UCN-01 across species and provide a perspective on how this information could be applied prospectively to the future development of this agent.
UCN - 01是一种正在研发的新型抗癌蛋白激酶抑制剂。患者的初始药理学特征并非由临床前实验预测得出。分布容积和全身清除率远低于实验动物(小鼠、大鼠和狗),消除半衰期异常长(>200小时)。人血浆中的游离分数也远小于狗、大鼠和小鼠,UCN - 01与人α-1酸性糖蛋白的结合比与人血清白蛋白或人γ-球蛋白的结合更强。α-1酸性糖蛋白与人血浆的缔合常数约为8×10⁸(mol/L)⁻¹,表明具有极高的亲和力。在这篇综述文章中,作者讨论了UCN - 01跨物种的药理学特征,并就如何将这些信息前瞻性地应用于该药物的未来开发提供了观点。