Instituto de Química, Universidade Federal de Goiás, 74690-900, Goiânia, GO, Brazil.
Laboratorio de Biosensores y Bioanálisis (LABB), Departamento de Química Biológica e IQUIBICEN - CONICET, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires (UBA), Pabellón 2, Ciudad Universitaria, Ciudad Autónoma de Buenos Aires, Argentina.
Anal Methods. 2023 Dec 21;16(1):33-39. doi: 10.1039/d3ay01739g.
Whisky adulteration is a prevalent practice driven by the high cost of these beverages. Counterfeiters commonly dilute whisky with less expensive alcoholic beverages, water, food additives, drugs or pharmaceuticals. Paracetamol (PAR), an analgesic drug that mitigates hangovers and headaches, is commonly used to adulterate whisky. Currently, the primary method for quantifying PAR levels is high-performance liquid chromatography, but this technique is both time consuming and usually generates more residues. In this context, the utilization of miniaturized and portable analytical devices becomes imperative for conducting point-of-care/need analyses. These devices offer several advantages, including portability, user-friendliness, low cost, and minimal material wastage. This study proposes the selective distance-based PAR quantification on whisky samples using a paper-based microfluidic analytical device (μPAD). Colorimetric detection on paper-based platforms offers great benefits such as affordability, portability, and the ability to detect PAR without complicated instrumentation. The optimal detection conditions were achieved by introducing 5 μL of a mixture containing 7.5 mmol L of Fe(III) and K[Fe(CN)] into the detection zone, along with 12 μL of whisky samples into the sample zone. The method exhibited linear behavior within the concentration range from 15 to 120 mg L, with a determination coefficient of 0.998. PAR was quantified in adulterated samples. The results obtained with the paper-based devices were compared with a referenced method, and no significant differences were observed at a confidence level of 95%. The μPAD allowed to determine 1 drop of pharmaceutical medicine PAR of 200 mg mL in 1 L of solution, demonstrating excellent sensitivity. This method offers cost-effective and rapid analysis, reducing the consumption of samples, reagents, and wastes. Consequently, it could be considered a viable and portable alternative for analyzing beverages at criminal scenes, customs, and police operations, thereby enhancing the field of forensics.
威士忌掺假是一种普遍存在的做法,其原因是这些饮料的成本高昂。造假者通常用更便宜的酒精饮料、水、食品添加剂、药物或药品稀释威士忌。对乙酰氨基酚(PAR)是一种缓解宿醉和头痛的止痛药物,常被用于掺假威士忌。目前,定量测定 PAR 水平的主要方法是高效液相色谱法,但该技术既耗时又通常会产生更多的残留物。在这种情况下,使用微型化和便携式分析设备对于进行即时/现场分析变得至关重要。这些设备具有便携性、用户友好性、低成本和最小材料浪费等优点。本研究提出了一种基于距离的选择性 PAR 定量方法,用于威士忌样品的分析,使用基于纸张的微流控分析装置(μPAD)。基于纸张的平台的比色检测具有成本效益高、便携性好、无需复杂仪器即可检测 PAR 等优点。通过将含有 7.5mmol/L Fe(III)和 K[Fe(CN)]的 5μL 混合物引入检测区,并将 12μL 的威士忌样品引入样品区,达到了最佳的检测条件。该方法在浓度范围为 15 至 120mg/L 内表现出线性行为,决定系数为 0.998。对掺假样品中的 PAR 进行了定量分析。用基于纸张的设备获得的结果与参考方法进行了比较,在置信水平为 95%时,没有观察到显著差异。μPAD 能够在 1L 溶液中检测到 1 滴 200mg/mL 的药物 PAR,显示出优异的灵敏度。该方法提供了经济高效和快速的分析,减少了样品、试剂和废物的消耗。因此,它可以被认为是在犯罪现场、海关和警察行动中分析饮料的一种可行和便携的替代方法,从而增强了法医学领域。