Zuo Rongjun, Li Feng, Parikh Sweta, Cao Li, Cooper Kirsten L, Hong Yulong, Liu Jin, Faris Ronald A, Li Daochuan, Wang Hongbing
Corning Life Sciences, Bedford, Massachusetts (R.Z., F.L., S.P., L.C., K.L.C.); Corning, Science and Technology, Corning, New York (Y.H., J.L., R.A.F.); and University of Maryland, School of Pharmacy, Baltimore, Maryland (D.L., H.W.)
Corning Life Sciences, Bedford, Massachusetts (R.Z., F.L., S.P., L.C., K.L.C.); Corning, Science and Technology, Corning, New York (Y.H., J.L., R.A.F.); and University of Maryland, School of Pharmacy, Baltimore, Maryland (D.L., H.W.).
Drug Metab Dispos. 2017 Feb;45(2):198-207. doi: 10.1124/dmd.116.072124. Epub 2017 Jan 6.
Metabolism enzyme induction-mediated drug-drug interactions need to be carefully characterized in vitro for drug candidates to predict in vivo safety risk and therapeutic efficiency. Currently, both the Food and Drug Administration and European Medicines Agency recommend using primary human hepatocytes as the gold standard in vitro test system for studying the induction potential of candidate drugs on cytochrome P450 (CYP), CYP3A4, CYP1A2, and CYP2B6. However, primary human hepatocytes are known to bear inherent limitations such as limited supply and large lot-to-lot variations, which result in an experimental burden to qualify new lots. To overcome these shortcomings, a renewable source of human hepatocytes (i.e., Corning HepatoCells) was developed from primary human hepatocytes and was evaluated for in vitro CYP3A4 induction using methods well established by the pharmaceutical industry. HepatoCells have shown mature hepatocyte-like morphology and demonstrated primary hepatocyte-like response to prototypical inducers of all three CYP enzymes with excellent consistency. Importantly, HepatoCells retain a phenobarbital-responsive nuclear translocation of human constitutive androstane receptor from the cytoplasm, characteristic to primary hepatocytes. To validate HepatoCells as a useful tool to predict potential clinical relevant CYP3A4 induction, we tested three different lots of HepatoCells with a group of clinical strong, moderate/weak CYP3A4 inducers, and noninducers. A relative induction score calibration curve-based approach was used for prediction. HepatoCells showed accurate prediction comparable to primary human hepatocytes. Together, these results demonstrate that Corning HepatoCells is a reliable in vitro model for drug-drug interaction studies during the early phase of drug testing.
对于候选药物,需要在体外仔细表征代谢酶诱导介导的药物相互作用,以预测体内安全性风险和治疗效果。目前,美国食品药品监督管理局和欧洲药品管理局均建议使用原代人肝细胞作为体外测试系统的金标准,用于研究候选药物对细胞色素P450(CYP)、CYP3A4、CYP1A2和CYP2B6的诱导潜力。然而,已知原代人肝细胞存在固有局限性,如供应有限和批次间差异大,这给鉴定新批次带来了实验负担。为克服这些缺点,从原代人肝细胞开发了一种可再生的人肝细胞来源(即康宁肝细胞),并使用制药行业成熟的方法对其进行体外CYP3A4诱导评估。康宁肝细胞呈现出成熟的肝细胞样形态,并对所有三种CYP酶的典型诱导剂表现出原代肝细胞样反应,一致性极佳。重要的是,康宁肝细胞保留了人组成型雄甾烷受体从细胞质向细胞核的苯巴比妥反应性易位,这是原代肝细胞的特征。为验证康宁肝细胞作为预测潜在临床相关CYP3A4诱导的有用工具,我们用一组临床强效、中度/弱效CYP3A4诱导剂和非诱导剂测试了三批不同的康宁肝细胞。采用基于相对诱导评分校准曲线的方法进行预测。康宁肝细胞显示出与原代人肝细胞相当的准确预测。总之,这些结果表明,康宁肝细胞是药物测试早期阶段药物相互作用研究的可靠体外模型。