Pharmacokinetics, Dynamics and Metabolism, Pfizer, Inc., Groton, CT 06340, USA.
Drug Metab Dispos. 2010 Dec;38(12):2147-56. doi: 10.1124/dmd.110.034637. Epub 2010 Sep 16.
Recent regulatory guidance suggests that metabolites identified in human plasma should be present at equal or greater levels in one of the animal species used in safety assessments. In this report, a high-performance liquid chromatography-tandem mass spectrometry method is described whereby quantitative comparisons of exposures to metabolites between species can be obtained in the absence of authentic standards of the metabolites, calibration curves, and other attributes of standard bioanalytical methods. This novel method was tested using six drug-metabolite combinations. Plasma samples from animals are mixed with control plasma from humans and vice versa to remove possible differential effects of matrices. Through multiple ion monitoring-triggered enhanced product ion (EPI) scans, all metabolites were qualitatively confirmed, and daughter ions were selected for the most sensitive mass transitions to trigger EPI scans. Direct comparisons of metabolites in animal versus human plasma were achieved by calculating the peak area ratios of the metabolites versus an internal standard. Linearity of instrument responses was established by serial dilution. A statistical analysis demonstrated that experimentally measured ratios of the parent and metabolites in rat versus human correlated well with the nominal ratios of concentrations using linear regression with an average slope of 0.99 ± 0.08 (r = 0.994 ± 0.005). This analysis showed that if the experimentally determined ratio of mass spectrometer responses is ≥ 2.0, then the actual exposure ratio is unity or greater (p < 0.01). This method offers time- and resource-sparing advantages to ascertaining metabolite exposure comparisons between humans and laboratory animal species. A strategy for application of this approach within standard drug development processes is described.
最近的监管指南建议,在用于安全性评估的动物物种之一中,应存在与人体血浆中鉴定出的代谢物同等或更高水平的代谢物。在本报告中,描述了一种高效液相色谱-串联质谱法,通过该方法,可以在没有代谢物的真实标准品、校准曲线和标准生物分析方法的其他属性的情况下,获得物种间代谢物暴露量的定量比较。该新方法通过六种药物-代谢物组合进行了测试。将动物的血浆样品与来自人类的对照血浆混合,反之亦然,以消除基质可能产生的差异影响。通过多离子监测触发增强产物离子 (EPI) 扫描,对所有代谢物进行定性确认,并选择最敏感的质量转移用于触发 EPI 扫描的子离子。通过计算代谢物与内标物的峰面积比,直接比较动物与人类血浆中的代谢物。通过连续稀释建立仪器响应的线性。统计分析表明,用人-鼠血浆中母体和代谢物的实测比值与使用线性回归(平均斜率为 0.99 ± 0.08,r = 0.994 ± 0.005)计算出的浓度名义比值具有很好的相关性。该分析表明,如果质谱仪响应的实测比值≥2.0,则实际暴露比值为 1 或更高(p < 0.01)。该方法在确定人类和实验室动物物种之间的代谢物暴露比较方面具有节省时间和资源的优势。描述了在标准药物开发过程中应用该方法的策略。