Lu C, Anderson L C, Fenske R A
Department of Environmental Health, School of Public Health and Community Medicine, University of Washington, Seattle 98195-7234, USA.
J Toxicol Environ Health. 1997 Feb 7;50(2):101-11. doi: 10.1080/009841097160519.
Current biological monitoring techniques are often unable to provide accurate estimates of pesticide dose in exposed worker populations. This study was conducted to investigate the feasibility of pesticide biomonitoring using saliva. Atrazine [2-chloro-4-ethylamino-6-(isopropylamino)-s-triazine], a member of the triazine herbicides, was selected to investigate salivary excretion following direct gastric administration in rats. Concentrations of atrazine in whole saliva and arterial plasma samples were determined by enzyme-linked immunosorbent assay (ELISA). Atrazine reached its highest level in both arterial plasma (238 micrograms/L) and whole saliva (157 micrograms/L) 35 min after administration of 105 mg/kg of atrazine, and then decreased with time in a parallel fashion. Although saliva atrazine levels were lower than levels in arterial plasma, there was a very high correlation between whole saliva and arterial plasma atrazine concentrations (r2 = .95). In addition, pharmacokinetic analysis suggested that salivary levels of atrazine can be used to predict concentrations of atrazine in plasma. The mean whole saliva/arterial plasma atrazine concentration ratio (S/P) was 0.66 +/- 0.11 (n = 20). The S/P ratios did not vary significantly over time, and were not affected by salivary flow rate. This study demonstrates that atrazine is transported into saliva, and that a relatively constant concentration ratio between whole saliva and arterial plasma is maintained. Because the salivary concentrations of atrazine are independent of variation in salivary flow rate, salivary monitoring of atrazine in humans may prove useful and practical. Finally, this study suggests that other pesticides with chemical and physical properties similar to those of atrazine can be monitored in saliva.
目前的生物监测技术往往无法准确估计接触农药的工人群体中的农药剂量。本研究旨在探讨使用唾液进行农药生物监测的可行性。选择三嗪类除草剂成员阿特拉津[2-氯-4-乙氨基-6-(异丙氨基)-s-三嗪],研究大鼠直接胃内给药后的唾液排泄情况。通过酶联免疫吸附测定(ELISA)测定全唾液和动脉血浆样本中阿特拉津的浓度。给予105mg/kg阿特拉津后35分钟,动脉血浆(238微克/升)和全唾液(157微克/升)中的阿特拉津均达到最高水平,然后随时间呈平行下降。虽然唾液中阿特拉津水平低于动脉血浆中的水平,但全唾液和动脉血浆中阿特拉津浓度之间存在非常高的相关性(r2 = 0.95)。此外,药代动力学分析表明,唾液中阿特拉津水平可用于预测血浆中阿特拉津的浓度。全唾液/动脉血浆阿特拉津浓度的平均比值(S/P)为0.66±0.11(n = 20)。S/P比值随时间无显著变化,且不受唾液流速影响。本研究表明阿特拉津可转运至唾液中,且全唾液与动脉血浆之间维持相对恒定的浓度比。由于唾液中阿特拉津浓度与唾液流速变化无关,对人体唾液中阿特拉津的监测可能证明是有用且实用的。最后,本研究表明其他化学和物理性质与阿特拉津相似的农药也可在唾液中进行监测。