Liu Xing, DeJesus Albert, Cao Zhisong, Vardeman Dana, Giovanella Beppino
CHRISTUS Stehlin Foundation for Cancer Research, 10301 Stella Link, Houston, TX 77025, USA.
Int J Mol Sci. 2012;13(5):5498-5505. doi: 10.3390/ijms13055498. Epub 2012 May 8.
CZ48, chemically camptothecin-20-O-propionate hydrate, is currently under clinical investigation. The kinetics of the metabolite camptothecin (CPT) formation and of CZ48 depletion in mouse and human liver microsomes in the presence or absence of NADPH was examined. The formation rate of camptothecin in human liver microsomes was significantly higher than that in mouse with mean K(m)s of 1.9 and 0.5 nM and V(max)s of 9.3 and 2.2 pmol/min/mg, respectively. However, the apparent intrinsic clearance (V(max)/K(m)) ratios for camptothecin in human and mouse liver microsomes were not significantly different from each other (4.9 versus 4.4) in the presence of NADPH. The depletion of CZ48 in human microsomes was four times faster with 4.55% of CZ48 remaining intact while in mouse 19.11% of the drug remained unchanged after 60 min. These results suggest that there is a remarkable species difference of CZ48 biotransformation between human and mouse. The depletion rate of CZ48 in human liver microsomes is considerably higher than that in the mouse.
CZ48,化学名称为喜树碱-20-O-丙酸盐水合物,目前正处于临床研究阶段。研究了在有或没有NADPH存在的情况下,小鼠和人肝微粒体中代谢产物喜树碱(CPT)的形成动力学以及CZ48的消耗情况。人肝微粒体中喜树碱的形成速率显著高于小鼠,其平均米氏常数(K(m))分别为1.9和0.5 nM,最大反应速率(V(max))分别为9.3和2.2 pmol/min/mg。然而,在存在NADPH的情况下,人及小鼠肝微粒体中喜树碱的表观内在清除率(V(max)/K(m))比值彼此无显著差异(分别为4.9和4.4)。人微粒体中CZ48的消耗速度快四倍,60分钟后仍有4.55%的CZ48保持完整,而在小鼠中,60分钟后仍有19.11%的药物未发生变化。这些结果表明,人和小鼠之间CZ48生物转化存在显著的种属差异。人肝微粒体中CZ48的消耗速率明显高于小鼠。