Limited sampling models for oral midazolam: Midazolam plasma concentrations, not the ratio of 1-hydroxymidazolam to midazolam plasma concentrations, accurately predicts AUC as a biomarker of CYP3A activity

被引:35
|
作者
Lee, LS
Bertino, JS
Nafziger, AN
机构
[1] Bassett Healthcare, Clin Pharmacol Res Ctr, Res Inst, Cooperstown, NY USA
[2] Bassett Healthcare, Dept Med, Cooperstown, NY USA
来源
JOURNAL OF CLINICAL PHARMACOLOGY | 2006年 / 46卷 / 02期
关键词
midazolam; cytochrome P-450 enzyme systems; predictive value of tests; pharmacokinetics; humans;
D O I
10.1177/0091270005283466
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oral midazolam is used as a phenotyping probe for cytochrome P450 (GYP) 3A activity and requires multiple plasma samples to measure drug exposure. Limited sampling is a useful strategy for optimizing sampling and reducing costs and labor. We studied limited sampling models using multiple linear regressions to predict the area under the concentration versus time curve (AUC) of midazolam using either midazolam plasma concentrations or the ratio of 1-hydroxymidazolam (1-OH MDZ) to midazolam plasma concentrations. CYP3A baseline activity data for oral midazolam from previous studies were used (45 healthy adults for models using midazolam plasma concentrations and 41 healthy adults for models using the ratios of 1-OH MDZ to midazolam [plasma concentrations). Limited sampling models were derived. validated, and evaluated for precision and bias. Two equations using the time points at 0.5 and 6 hours and 0.5, 2, and 6 hours were acceptable and predictive of midazolam AUC using midozolam plasma concentrations. No 1-OH MDZ to midazolam plasma concentration ratios accurately predicted midazolam AUC.
引用
收藏
页码:229 / 234
页数:6
相关论文
共 16 条
  • [1] Single plasma sampling to predict oral clearance of CYP3A probe midazolam
    Zhu, B
    Ou-Yang, DS
    Cheng, ZN
    Huang, SL
    Zhou, HH
    ACTA PHARMACOLOGICA SINICA, 2001, 22 (07): : 634 - 638
  • [2] Evaluation of limited sampling models for prediction of oral midazolam AUC for CYP3A phenotyping and drug interaction studies
    Silke C. Mueller
    Bernd Drewelow
    European Journal of Clinical Pharmacology, 2013, 69 : 1127 - 1134
  • [3] Evaluation of limited sampling models for prediction of oral midazolam AUC for CYP3A phenotyping and drug interaction studies
    Mueller, Silke C.
    Drewelow, Bernd
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2013, 69 (05) : 1127 - 1134
  • [4] Proposal of a new limited sampling strategy to predict CYP3A activity using a partial AUC of midazolam
    Katzenmaier, Stephanie
    Markert, Christoph
    Mikus, Gerd
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2010, 66 (11) : 1137 - 1141
  • [5] Proposal of a new limited sampling strategy to predict CYP3A activity using a partial AUC of midazolam
    Stephanie Katzenmaier
    Christoph Markert
    Gerd Mikus
    European Journal of Clinical Pharmacology, 2010, 66 : 1137 - 1141
  • [6] Treatment with rilpivirine does not alter plasma concentrations of the CYP3A substrates tadalafil and midazolam in humans
    Hohmann, Nicolas
    Reinhard, Raphael
    Schnaidt, Sven
    Witt, Lukas
    Carls, Alexandra
    Burhenne, Jurgen
    Mikus, Gerd
    Haefeli, Walter E.
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2016, 71 (08) : 2241 - 2247
  • [7] Serum Alanine Transaminase Total Bilirubin Concentrations Predict CYP3A Activity as Measured by Midazolam and 1′-Hydroxylation
    He, Rui
    Li, Yuhong
    Ruan, Jinguang
    MEDICAL SCIENCE MONITOR, 2015, 21 : 396 - 402
  • [8] A developed determination of midazolam and 1'-hydroxymidazolam in plasma by liquid chromatography-mass spectrometry: Application of human pharmacokinetic study for measurement of CYP3A activity
    Shimizu, Mikiko
    Uno, Tsukasa
    Tamura, Hiro-omi
    Kanazawa, Hideko
    Murakami, Isao
    Sugawara, Kazunobu
    Tateishi, Tomonori
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2007, 847 (02): : 275 - 281
  • [9] Quantification of femtomolar concentrations of the CYP3A substrate midazolam and its main metabolite 1'-hydroxymidazolam in human plasma using ultra performance liquid chromatography coupled to tandem mass spectrometry
    Burhenne, Juergen
    Halama, Birte
    Maurer, Monika
    Riedel, Klaus-Dieter
    Hohmann, Nicolas
    Mikus, Gerd
    Haefeli, Walter E.
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2012, 402 (07) : 2439 - 2450
  • [10] Quantification of femtomolar concentrations of the CYP3A substrate midazolam and its main metabolite 1′-hydroxymidazolam in human plasma using ultra performance liquid chromatography coupled to tandem mass spectrometry
    Jürgen Burhenne
    Birte Halama
    Monika Maurer
    Klaus-Dieter Riedel
    Nicolas Hohmann
    Gerd Mikus
    Walter E. Haefeli
    Analytical and Bioanalytical Chemistry, 2012, 402 : 2439 - 2450