Urine as a biological specimen for forensic analysis of alcohol and variability in the urine-to-blood relationship.

Alan W Jones
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引用次数: 74

Abstract

This article concerns the use of urine as a biological specimen for determination of alcohol in clinical and forensic toxicology and discusses factors that might influence variability in the urine/blood concentration ratio of alcohol. A large number of human drinking experiments were conducted to determine the time course of urine-alcohol concentrations (UAC) in relation to blood-alcohol concentrations (BAC). The UAC and BAC curves were shifted in time and the BAC curve always began to decrease before the UAC started to decline. During the early absorption phase the UAC/BAC ratio was less than unity, whereas in the late absorption/distribution period the ratio was between 1.0-1.2. On reaching the post-absorptive phase, the UAC always exceeded BAC and UAC/BAC ratios averaged 1.3-1.4, increasing appreciably as BAC decreased towards zero. Alcohol-induced diuresis was most pronounced during the rising portion of the BAC curve and near to the peak value. After about 2 hours post-drinking, the production rate of urine diminished to the pre-drinking rate of about 0.5-1 mL/min. Drinking water during the post-absorptive phase of the alcohol curve produced dilute urine, as reflected in lower creatinine content and osmolality, although the concentration of ethanol remained unchanged. After subjects drank a moderate dose of ethanol (0.54-0.85 g/kg) about 2% of the dose was recoverable in the urine after 7 hours. Ethyl glucuronide, a minor metabolite of ethanol, was measured in urine samples from drunk drivers. The UAC/BAC ratio of ethanol in drunk drivers did not depend on the creatinine content of the urine and therefore the relative dilution of the specimens. When alcohol-free urine was spiked with glucose and infected with the yeast species Candida albicans, ethanol was produced by fermentation after approximately 24 hours storage at room temperature. This post-sampling synthesis of ethanol was prevented by sodium fluoride (1% weight by volume) in the urine tubes or by keeping the specimens in the cold (4 degrees C). The UAC and BAC were highly correlated (r > 0.95) in drunk drivers and in autopsy cases, although the residual standard deviations were appreciable. This speaks against attempting to estimate BAC indirectly from UAC in any individual case. The UAC/BAC ratio and the change in UAC between two successive voids can help to resolve whether a large amount of alcohol had recently been consumed. This information is useful to support or challenge allegations of drinking alcohol after driving, which has become known as the hip-flask defence.

尿液作为酒精和尿液-血液关系变异性法医分析的生物标本。
本文讨论了在临床和法医毒理学中使用尿液作为测定酒精的生物标本,并讨论了可能影响尿液/血液酒精浓度比变异性的因素。为了确定尿酒精浓度(UAC)与血酒精浓度(BAC)的关系,进行了大量人体饮酒实验。UAC和BAC曲线随时间发生位移,BAC曲线总是在UAC开始下降之前开始下降。在吸收前期,UAC/BAC小于1,而在吸收/分配后期,该比值在1.0 ~ 1.2之间。进入吸收后阶段,UAC始终超过BAC, UAC/BAC比值平均为1.3 ~ 1.4,随着BAC趋于零,UAC/BAC比值明显增加。酒精引起的利尿在BAC曲线上升部分和接近峰值时最为明显。饮后约2小时,尿产率降至饮前0.5-1 mL/min左右。在酒精曲线的吸收后阶段,饮用水产生稀释的尿液,反映在较低的肌酐含量和渗透压,尽管乙醇浓度保持不变。受试者饮用中等剂量的乙醇(0.54-0.85 g/kg)后,约2%的剂量可在7小时后从尿液中恢复。葡萄糖醛酸乙酯是乙醇的一种微量代谢物,在醉酒司机的尿液样本中进行了检测。醉酒司机体内乙醇的UAC/BAC比率不依赖于尿液中肌酐的含量,因此不依赖于样本的相对稀释度。当不含酒精的尿液中加入葡萄糖并感染白色念珠菌时,在室温下保存约24小时后发酵产生乙醇。通过在尿管中添加氟化钠(体积重量比为1%)或将标本保存在低温(4摄氏度)中,可以阻止这种取样后乙醇的合成。UAC和BAC在酒后驾驶和尸检案例中高度相关(r > 0.95),尽管残留标准偏差相当可观。这反对在任何个别情况下试图从UAC间接估计BAC。UAC/BAC比率以及连续两次空隙之间UAC的变化可以帮助判断最近是否摄入了大量酒精。这一信息对于支持或质疑驾车后饮酒的指控是有用的,这种指控被称为“髋瓶辩护”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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