Gaudreault J, Potvin D, Lavigne J, Lalonde R L
Phoenix International Life Sciences Inc, Saint-Laurent, Québec, Canada.
Pharm Res. 1998 Oct;15(10):1621-9. doi: 10.1023/a:1011971620661.
The use of truncated areas under the curve (AUCs) could be a significant advantage for bioequivalence studies of drugs with long half-lives. The purpose of this study was to evaluate the performance of truncated AUCs as measures of relative extent of bioavailability using a large database of experimental data and Monte Carlo simulations.
The experimental data consisted of 123 single-dose, 2-treatment, crossover studies with at least 18 subjects/study. Monte Carlo techniques were also used to simulate studies that reflected a wide variety of experimental conditions. AUCs were calculated over different time intervals and the standard two one-sided t tests procedure was used to assess bioequivalence.
The experimental data showed that conclusions concerning bioequivalence were identical between AUCs truncated at four times the time of peak concentration (Tmax) and AUCs extrapolated to infinity (AUC(inf)) in 120/123 or 97.6% of studies. There was little change in the intra-subject CVs for AUCs truncated at 3*Tmax or later. The results of Monte Carlo simulations were generally consistent with the experimental data and showed that AUCs truncated at 72 hours (AUC(0-72)) performed well compared to AUC(inf) as measures of bioequivalence for drugs with long half-lives.
Based on both the experimental and simulated data, AUCs truncated after the absorption phase perform well as measures of relative extent of bioavailability. Truncated AUCs offer a particular advantage for drugs with long half-lives and these results indicate that it would be reasonable to limit the sample collection period to 72 hours in bioequivalence studies of oral formulations.
对于半衰期较长的药物进行生物等效性研究时,使用曲线下截尾面积(AUC)可能具有显著优势。本研究的目的是利用大量实验数据和蒙特卡洛模拟,评估截尾AUC作为生物利用度相对程度指标的性能。
实验数据包括123项单剂量、双治疗、交叉研究,每项研究至少有18名受试者。还使用蒙特卡洛技术模拟反映各种实验条件的研究。在不同时间间隔计算AUC,并使用标准的双单侧t检验程序评估生物等效性。
实验数据表明,在120/123项或97.6%的研究中,在峰浓度时间(Tmax)的四倍处截尾的AUC与外推至无穷大的AUC(AUC(inf))之间关于生物等效性的结论是相同的。在3*Tmax或更晚时间截尾的AUC的受试者内CV变化很小。蒙特卡洛模拟结果总体上与实验数据一致,表明对于半衰期较长的药物,在72小时处截尾的AUC(AUC(0 - 72))作为生物等效性指标与AUC(inf)相比表现良好。
基于实验和模拟数据,吸收相后截尾的AUC作为生物利用度相对程度的指标表现良好。截尾AUC对于半衰期较长的药物具有特别的优势,这些结果表明在口服制剂的生物等效性研究中将样本采集期限制在72小时是合理的。