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Analyzing Wastewater Samples Collected during Census To Determine the Correction Factors of Drugs for Wastewater-Based Epidemiology: The Case of Codeine and Methadone

机译:分析人口普查期间收集的废水样品,以确定废水流体流学药物矫正因子:可待因和美沙酮的情况

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摘要

The correction factor (CF) is a critical parameter for back estimating the consumption of a drug via wastewater-based epidemiology (WBE). The CF is usually the excretion factor (EF) of the drug or metabolite (the fraction of drug excreted after consumption and the molecular mass ratio of parent drug/metabolite) traditionally determined by human pharmacokinetic studies. An alternative approach to derive CFs is to compare the consumption data with the loads measured by WBE in representative wastewater samples. For this purpose, during the 2016 Australian Census week, more than 500 wastewater samples were collected from 83 wastewater treatment plants across Australia (covering >60% of the Australian population) and analyzed for codeine, methadone, and methadone metabolite, EDDP. National sales data for codeine and methadone to local pharmacies were obtained to estimate the CFs for the three biomarkers. The CFs estimated for codeine and EDDP in this study, 29% (95% CI = 28%-30%) and 50% (95% CI = 49%-52%), respectively, are significantly different from the EFs deduced from pharmacokinetic data (60% and 25%), while methadone's CF is relatively similar to previously used values (22% vs 27.5%). The newly derived CFs were applied to available data in the literature and produced better matches between estimates and consumption data than previously reported. It is thus suggested that the new approach be used to derive the CFs of other drugs of interest for WBE application when limited pharmacokinetic data are available.
机译:校正因子(CF)是通过废水的流行病学(WBE)返回估计药物消耗的关键参数。 CF通常是药物或代谢物的排泄因子(EF)(消耗后的药物的级分,以及母体药物/代谢物的分子质量比)传统上由人类药代动力学研究确定。派生CFS的替代方法是将消费数据与由代表性废水样本中的WBE测量的负载进行比较。为此目的,在2016年澳大利亚人口普查周期间,从澳大利亚的83个废水处理厂收集了超过500种废水样本(覆盖> 60%的澳大利亚人口),并分析为可待因,美沙酮和美沙酮代谢物,EDDP。获得了可待因和美沙酮的国家销售数据,得到了当地药店,以估计三个生物标志物的CFS。本研究估计的CFS和EDDP估计,29%(95%CI = 28%-30%)和50%(95%CI = 49%-52%)与药代动力学引用的EF显着不同数据(60%和25%),而美沙酮的CF与先前使用的值相对相似(22%vs 27.5%)。新派生的CFS应用于文献中的可用数据,并在估计和消费数据之间产生比以前报告的更好的匹配。因此,建议在有限的药代动力学数据可用时,用于推导出WBE应用的其他目的药物的CFS。

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