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线性消除阶段血液酒精浓度/呼气酒精浓度(BAC/BrAC)转换因子的浓度依赖性

Concentration dependency of the BAC/BrAC (blood alcohol concentration/breath alcohol concentration) conversion factor during the linear elimination phase.

作者信息

Haffner H T, Graw M, Dettling A, Schmitt G, Schuff A

机构信息

Institut für Rechts- und Verkehrsmedizin, Verkehrsmedizin/Verkehrspsychologie, Bergheimer Strasse 147, 69115, Heidelberg, Germany.

出版信息

Int J Legal Med. 2003 Oct;117(5):276-81. doi: 10.1007/s00414-003-0384-5. Epub 2003 Jul 5.

DOI:10.1007/s00414-003-0384-5
PMID:12845448
Abstract

According to the theoretical pharmacokinetical considerations put forward by Wehner et al. the BAC(ven)/BrAC conversion factor Q is not a constant value and varies depending on the pharmacokinetic phase deduced from the alcohol concentration curve. Based on these considerations we propose that Q must be inversely proportional to the BrAC during the postabsorptive linear elimination phase, expressed as the hyperbola Q=1/kappa+(CT)/BrAC. The constants kappa or 1/kappa and (CT)--where (CT) consists of different parameters which remain constant during the linear elimination phase--can be experimentally determined from the linear relationship BrAC = kappaBAC(ven)-kappa(CT). To test this hypothesis 12 human volunteers received parenteral doses of ethanol. During the elimination phase, BAC and BrAC of each volunteer were measured between 18 and 34 times in a BrAC range between 0.65 mg/l and 0.12 mg/l. The conversion factor Q was either expressed in the form of the hyperbola Q=1/kappa+(CT)/BrAC or directly calculated from the ratio BAC(ven)/BrAC and the results obtained using both methods were found to be very similar. The values of 1/kappa of the hyperbolic functions varied between 1.808 and 2.165 and those of (CT) between 0.004 and 0.127. For a BrAC of 0.25 mg/l, an average value of 2.308+/-0.080 could be calculated for the conversion factor Q(0.25). On average, the value of Q(0.40) amounted to 2.207+/-0.048 and that of Q(0.55) to 2.160+/-0.056.

摘要

根据韦纳等人提出的理论药代动力学考量,血液酒精浓度(静脉血)/呼出气体酒精浓度转换因子Q并非恒定值,而是会根据从酒精浓度曲线推导得出的药代动力学阶段而变化。基于这些考量,我们提出,在吸收后线性消除阶段,Q必须与呼出气体酒精浓度成反比,可表示为双曲线Q = 1/κ+(CT)/呼出气体酒精浓度。常数κ或1/κ以及(CT)(其中(CT)由线性消除阶段保持恒定的不同参数组成)可通过线性关系呼出气体酒精浓度 = κ血液酒精浓度(静脉血)-κ(CT)进行实验测定。为验证这一假设,12名人类志愿者接受了乙醇的肠胃外给药。在消除阶段,对每位志愿者的血液酒精浓度和呼出气体酒精浓度在呼出气体酒精浓度范围为0.65毫克/升至0.12毫克/升之间进行了18至34次测量。转换因子Q要么以双曲线Q = 1/κ+(CT)/呼出气体酒精浓度的形式表示,要么直接通过血液酒精浓度(静脉血)/呼出气体酒精浓度的比值计算得出,结果发现使用这两种方法得到的结果非常相似。双曲线函数的1/κ值在1.808至2.165之间变化,(CT)的值在0.004至0.127之间变化。对于呼出气体酒精浓度为0.25毫克/升的情况,转换因子Q(0.25)的平均值可计算为2.308±0.080。平均而言,Q(0.40)的值为2.207±0.048,Q(0.55)的值为2.160±0.056。

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