通过表面增强拉曼光谱检测可卡因、摇头丸、甲基苯丙胺和咖啡因混合物中的低浓度芬太尼。

Journal of forensic sciences Pub Date : 2025-01-01 Epub Date: 2024-11-11 DOI:10.1111/1556-4029.15652
Saiqa Muneer, Matthew Smith, Mikaela M Bazley, Daniel Cozzolino, Joanne T Blanchfield
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引用次数: 0

摘要

利用表面增强拉曼光谱(SERS)测量了混合在常见切割剂、可卡因、3,4-亚甲二氧基甲基苯丙胺(MDMA)、甲基苯丙胺和咖啡因中的低浓度芬太尼。混合物的芬太尼浓度范围为 0-339 μM。数据分析的最初方法是绘制诊断峰(1026 cm-1)面积与浓度的关系图,以生成校准模型。这种方法对芬太尼/MDMA 样品(LOD 0.04 μM)成功,但对其他混合物则不成功。然后采用了化学计量学方法。使用主成分分析 (PCA)、偏最小二乘法 (PLS1) 回归和线性判别分析 (LDA) 对数据进行了评估。线性判别分析模型用于将样品分为三个指定浓度范围,低 = 0-0.4 mM、中 = 0.4-14 mM 或高 >14 mM,芬太尼浓度的正确分类准确率超过 85%。然后使用一系列 "盲 "芬太尼混合物对该模型进行了验证,这些未知样本被归入了正确的浓度范围,准确率大于 95%。PLS1 模型未能为样品提供准确的定量分配,但对芬太尼的存在与否提供了准确的预测。这两个模型的结合实现了对二元混合物中芬太尼的准确定量分配。这项工作建立了一个概念证明,表明更大的样本量可以生成更准确的模型。它证明了使用 SERS 可以对含有不同低浓度芬太尼的样品进行精确定量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of low-level fentanyl concentrations in mixtures of cocaine, MDMA, methamphetamine, and caffeine via surface-enhanced Raman spectroscopy.

Surface-enhanced Raman spectroscopy (SERS) was utilized to measure low-level fentanyl concentrations mixed in common cutting agents, cocaine, 3,4-methylenedioxymethamphetamine (MDMA), methamphetamine, and caffeine. Mixtures were prepared with a fentanyl concentration range of 0-339 μM. Data was initially analyzed by plotting the area of a diagnostic peak (1026 cm-1) against concentration to generate a calibration model. This method was successful with fentanyl/MDMA samples (LOD 0.04 μM) but not for the other mixtures. A chemometric approach was then employed. The data was evaluated using principal component analysis (PCA), partial least squares (PLS1) regression, and linear discriminant analysis (LDA). The LDA model was used to classify samples into one of three designated concentration ranges, low = 0-0.4 mM, medium = 0.4-14 mM, or high >14 mM, with fentanyl concentrations correctly classified with greater than 85% accuracy. This model was then validated using a series of "blind" fentanyl mixtures and these unknown samples were assigned to the correct concentration range with an accuracy >95%. The PLS1 model failed to provide accurate quantitative assignments for the samples but did provide an accurate prediction for the presence or absence of fentanyl. The combination of the two models enabled accurate quantitative assignment of fentanyl in binary mixtures. This work establishes a proof of concept, indicating a larger sample size could generate a more accurate model. It demonstrates that samples, containing variable, low concentrations of fentanyl, can be accurately quantified, using SERS.

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