Breimer L T, Burm A G, Danhof M, Hennis P J, Vletter A A, de Voogt J W, Spierdijk J, Bovill J G
Department of Anaesthesiology, University of Leiden, The Netherlands.
Clin Pharmacokinet. 1991 Jun;20(6):497-508. doi: 10.2165/00003088-199120060-00006.
The CNS effects resulting from the combined administration of midazolam and flumazenil were studied in 8 healthy volunteers to develop a model of the pharmacokinetic-pharmacodynamic interaction. Electroencephalograms (EEG) were recorded between Fp1-M1 and Fp2-M2. The EEG parameter total number of waves between 12 and 30 Hz (TNW12-30) derived by aperiodic analysis was used to quantify the effect. Following a 15 min baseline EEG recording, infusion of placebo or flumazenil was started. Infusion regimens for flumazenil were designed so that 'steady-state' concentrations of 10 and 20 micrograms/L were obtained. Doses of midazolam 15, 30 and 60 mg over 5 min were given 30 min after the start of placebo infusion (session A) or flumazenil infusion to 10 micrograms/L (session B) or 20 micrograms/L (session C), respectively. Venous blood samples were taken until 8 h after the start of the flumazenil or placebo infusion. A sigmoid maximum effect (Emax) model was used to characterise the relationship between the plasma concentration of midazolam which is in equilibrium with the effect compartment concentration (Cem) [Cem/Kp] and TNW12-30. Within 2 to 5 min of starting the midazolam infusion all subjects fell asleep, with loss of eyelid reflex. They awoke between 25 and 82 min later in all 3 sessions. The mean (+/- SD) plasma drug concentrations of midazolam corresponding to half the maximum increase in TNW12-30 (EC50) were 276 +/- 64, 624 +/- 187 and 1086 +/- 379 micrograms/L in sessions A, B and C, respectively. The half-lives reflecting equilibration between plasma concentration and effect (t1/2ke0), estimated by a nonparametric method, were 2.2 +/- 1.2, 3.3 +/- 3.3 and 2.9 +/- 1.2 min for the 3 different sessions. Emax and N were not affected by flumazenil. In each subject the plot of the average measured steady-state plasma flumazenil concentration versus the EC50 of midazolam showed a linear relationship. The plasma concentration of flumazenil that doubled the EC50 of midazolam (Cf,2) was 6.5 +/- 1.0 micrograms/L. The observed interaction is consistent with the competitive nature of the antagonism of midazolam by flumazenil.
在8名健康志愿者中研究了咪达唑仑和氟马西尼联合给药产生的中枢神经系统效应,以建立药代动力学-药效学相互作用模型。在Fp1-M1和Fp2-M2之间记录脑电图(EEG)。通过非周期性分析得出的12至30Hz之间的脑电波总数(TNW12-30)这一EEG参数用于量化效应。在进行15分钟的基线EEG记录后,开始输注安慰剂或氟马西尼。设计氟马西尼的输注方案,以便获得10和20μg/L的“稳态”浓度。在安慰剂输注开始30分钟后(A session),或分别在氟马西尼输注至10μg/L(B session)或20μg/L(C session)后,在5分钟内给予15、30和60mg咪达唑仑剂量。在氟马西尼或安慰剂输注开始后直至8小时采集静脉血样。采用S形最大效应(Emax)模型来描述与效应室浓度(Cem)处于平衡状态的咪达唑仑血浆浓度(Cem/Kp)与TNW12-30之间的关系。在开始咪达唑仑输注的2至5分钟内,所有受试者均入睡,眼睑反射消失。在所有3个试验中,他们在25至82分钟后醒来。在A、B和C试验中,对应于TNW12-30最大增加量一半(EC50)的咪达唑仑平均(±标准差)血浆药物浓度分别为276±64、624±187和1086±379μg/L。通过非参数方法估计的反映血浆浓度与效应之间平衡的半衰期(t1/2ke0),在3个不同试验中分别为2.2±1.2、3.3±3.3和2.9±1.2分钟。Emax和N不受氟马西尼影响。在每个受试者中,平均测得的稳态血浆氟马西尼浓度与咪达唑仑的EC50的关系图呈线性关系。使咪达唑仑的EC50加倍的氟马西尼血浆浓度(Cf,2)为6.5±1.0μg/L。观察到的相互作用与氟马西尼对咪达唑仑拮抗作用的竞争性性质一致。