Curvall M, Vala E K, Enzell C R, Wahren J
Research Department, Swedish Tobacco Co., Stockholm.
Clin Pharmacol Ther. 1990 Jan;47(1):42-9. doi: 10.1038/clpt.1990.6.
The technique of monitoring cotinine concentrations in body fluids as a means of measuring nicotine intake during passive smoking has been evaluated in two studies, both of which used intravenous infusion to stimulate nicotine intake. In the first study, nicotine and cotinine were given separately, for 1 hour in four different intravenous doses (3.2, 15.4, 30.9, and 61.7 nmol/min) to each nonsmoker. In the second study, nicotine and cotinine were infused for 4 hours; each subject received five different doses of nicotine (1.5, 3.1, 6.2, 10.8, and 15.4 nmol/min) and one of cotinine (10.8 nmol/min). The concentration of cotinine was constant in both plasma and saliva from 1 to 4 hours after the nicotine infusion; the plateau levels of cotinine were found to be linearly and directly related to the nicotine intake. The ratio of salivary to plasma cotinine was 1:1.27. A linear relationship was also found between nicotine and cotinine infusion rates and the AUC values for cotinine. The fraction metabolized to cotinine was found to be about 0.5. The results from these studies show that: (1) there is a linear relationship between the plateau concentration of cotinine and the amount of nicotine infused over a period of 1 up to 4 hours; (2) salivary cotinine provides the same information on nicotine intake as does plasma cotinine; and (3) single measurements of either plasma or salivary cotinine concentrations at 1 to 4 hours after the exposure could be used to predict the nicotine intake during 1 to 4 hours of environmental tobacco smoke exposure.
有两项研究对通过监测体液中可替宁浓度来测量被动吸烟期间尼古丁摄入量的技术进行了评估,这两项研究均采用静脉输注来刺激尼古丁摄入。在第一项研究中,分别向每位不吸烟者静脉注射尼古丁和可替宁,每种药物以四种不同的静脉注射剂量(3.2、15.4、30.9和61.7纳摩尔/分钟)持续注射1小时。在第二项研究中,尼古丁和可替宁输注4小时;每位受试者接受五种不同剂量的尼古丁(1.5、3.1、6.2、10.8和15.4纳摩尔/分钟)和一种剂量的可替宁(10.8纳摩尔/分钟)。在尼古丁输注后1至4小时内,血浆和唾液中的可替宁浓度保持恒定;发现可替宁的平台期水平与尼古丁摄入量呈线性直接相关。唾液与血浆中可替宁的比例为1:1.27。还发现尼古丁和可替宁的输注速率与可替宁的AUC值之间存在线性关系。发现代谢为可替宁的部分约为0.5。这些研究的结果表明:(1)在1至4小时内,可替宁的平台期浓度与输注的尼古丁量之间存在线性关系;(2)唾液可替宁提供的关于尼古丁摄入量的信息与血浆可替宁相同;(3)在接触后1至4小时对血浆或唾液中可替宁浓度进行单次测量,可用于预测在1至4小时环境烟草烟雾接触期间的尼古丁摄入量。