Piekoszewski W, Gubała W
Institute of Forensic Research, Kraków, Poland.
Pol J Pharmacol. 2000 Sep-Oct;52(5):389-95.
In most research, the inter- and intra-individual variability of time profiles of ethanol concentration has been studied over a relatively short period of time. We present a study of inter- and intra-individual variability of ethanol pharmacokinetics in five healthy volunteers (social drinkers) over a period of around eight years. The volunteers received a dose of 0.7 g/kg (men) and 0.6 g/kg (women) of ethanol in the form of vodka diluted with mineral water. The blood ethanol concentrations in a series of samples were measured by gas chromatography. For pharmacokinetic calculations, a model with first-order absorption and Michaelis-Menten elimination was applied. A linear regression technique was used to calculate Widmark's coefficient. The area under the concentration-time curve (AUC) was calculated by trapezoid rule. A tendency for pharmacokinetic parameters to alter during the study time was observed, however, these changes were random and did not correlate with the duration of the study. The highest inter- and intra-subject variability of the half time of absorption was observed. The maximal elimination velocity and Michaelis-Menten constant were also very unstable; coefficients of variation were 55.8% and 79.0%, respectively. Other calculated pharmacokinetic parameters (AUC, beta60, V/F, Cmax) were characterized by a lower variability with a coefficient of variation around 36%. Back extrapolation of plasma ethanol concentration using mean value of beta60 for each subject showed that results could be underestimated up to 26% or overestimated up to 102%.
在大多数研究中,乙醇浓度时间曲线的个体间和个体内变异性是在相对较短的时间内进行研究的。我们呈现了一项对五名健康志愿者(社交饮酒者)在大约八年时间内乙醇药代动力学个体间和个体内变异性的研究。志愿者以用矿泉水稀释的伏特加形式接受了0.7 g/kg(男性)和0.6 g/kg(女性)的乙醇剂量。通过气相色谱法测量一系列样本中的血液乙醇浓度。对于药代动力学计算,应用了具有一级吸收和米氏消除的模型。使用线性回归技术计算维德马克系数。通过梯形法则计算浓度-时间曲线下面积(AUC)。在研究期间观察到药代动力学参数有改变的趋势,然而,这些变化是随机的,并且与研究持续时间无关。观察到吸收半衰期的个体间和个体内变异性最高。最大消除速度和米氏常数也非常不稳定;变异系数分别为55.8%和79.0%。其他计算的药代动力学参数(AUC、β60、V/F、Cmax)的特征是变异性较低,变异系数约为36%。使用每个受试者β60的平均值对血浆乙醇浓度进行反向外推表明,结果可能被低估高达26%或高估高达102%。