Adams J D, Lavoie E J, O'Donnell M, Hoffmann D
IARC Sci Publ. 1984(57):779-85.
Methods were developed to determine the biological half-life of N'-nitrosonornicotine (NNN) and 4-(N-nitrosomethylamino)-1-(3-pyridyl)-1-butanone (NNK) in Syrian golden hamsters and Fischer rats. The formation and elimination of 4-(N-nitrosomethylamino)-1-(-3-pyridyl)-1-butanol (NNA1), the major metabolite of NNK, was determined in the context of this study. The method consisted of extraction of the nitrosamine with ethyl acetate, elution through a Clin-Elut column, and concentration of the sample, followed by gas chromatography-thermal energy analysis. Biological half-lives of NNN, NNK and NNA1 in hamsters were found to be 0.77, 0.25 and 1.78 h, respectively; in rats they were 5.78, 1.78 and 3.56 h. These findings clearly indicate species differences in the pharmacokinetics associated with the distribution and elimination of the tobacco-specific N-nitrosamines.
已开发出测定叙利亚金黄地鼠和费希尔大鼠体内N'-亚硝基降烟碱(NNN)和4-(N-亚硝基甲基氨基)-1-(3-吡啶基)-1-丁酮(NNK)生物半衰期的方法。在本研究中测定了NNK的主要代谢产物4-(N-亚硝基甲基氨基)-1-(-3-吡啶基)-1-丁醇(NNA1)的形成和消除情况。该方法包括用乙酸乙酯萃取亚硝胺、通过Clin-Elut柱洗脱以及样品浓缩,随后进行气相色谱-热能分析。结果发现,NNN、NNK和NNA1在仓鼠体内的生物半衰期分别为0.77、0.25和1.78小时;在大鼠体内分别为5.78、1.78和3.56小时。这些发现清楚地表明,在与烟草特异性N-亚硝胺的分布和消除相关的药代动力学方面存在种属差异。