ETH Zurich, Institute for Quantum Electronics, Zurich, Switzerland.
Drug Test Anal. 2012 Jun;4(6):420-9. doi: 10.1002/dta.346. Epub 2011 Nov 24.
The consumption of drugs is of great concern worldwide. Various drug tests for humans have been developed but there is no compact and easy-to-use test device available yet for direct semi-quantitative drug testing in the field. We suggest using attenuated total reflection (ATR) infrared spectroscopy as a sensing method to analyze human saliva samples with respect to drugs. In this paper, we present ATR spectra in the infrared range between 2300 and 900 cm(-1) as a first step towards such a device. We emphasize the common drug cocaine and its metabolites and investigate the problems of spectral interferences of selected diluents, masking agents, common medication, and soft drinks. Furthermore, spectra of saliva samples are recorded and a time-dependent change of the spectral signatures after alcohol consumption is presented. To the best of our knowledge, it is the first time that not only spectra of the drug of interest (cocaine) dissolved in water and in saliva but also spectra of interfering compounds possibly present in the saliva sample of a tested subject are discussed. This paper presents the most appropriate spectral range for strong cocaine absorption (including its metabolites) and minimum interference by the investigated substances. This spectral window is found to be between 1800 and 1710 cm(-1). In addition, we demonstrate the feasibility to identify cocaine in saliva at a concentration of 0.020 mg/ml with IR-ATR-spectroscopy without any separation or extraction procedures. For example, this technique could also be applied for drug detection in waste water.
毒品的消费在全球范围内受到高度关注。已经开发出各种用于人体的毒品检测方法,但目前还没有用于现场直接半定量毒品检测的紧凑型易用测试设备。我们建议使用衰减全反射(ATR)红外光谱作为一种传感方法,分析人类唾液样本中的药物。在本文中,我们提出了在 2300 至 900 cm(-1) 之间的红外范围内的 ATR 光谱,作为开发此类设备的第一步。我们强调了常见药物可卡因及其代谢物,并研究了所选稀释剂、掩蔽剂、常见药物和软饮料的光谱干扰问题。此外,还记录了唾液样本的光谱,并呈现了酒精消耗后光谱特征的时间依赖性变化。据我们所知,这是第一次不仅讨论了溶解在水和唾液中的目标药物(可卡因)的光谱,还讨论了可能存在于被测受试者唾液样本中的干扰化合物的光谱。本文提出了用于强可卡因吸收(包括其代谢物)的最佳光谱范围,以及受研究物质干扰最小的光谱范围。该光谱窗口位于 1800 至 1710 cm(-1) 之间。此外,我们证明了无需任何分离或提取程序,使用 IR-ATR 光谱在唾液中以 0.020 mg/ml 的浓度识别可卡因的可行性。例如,该技术还可以应用于废水中的药物检测。