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Rapid and efficient identification of the precise isomeric form of new psychoactive substances (NPS) by forensic casework laboratories is a relevant challenge in the forensic field. Differences in legal status occur for ring-isomeric species of the same class, thus leading to different penalties and judicial control. Portable systems such as near-infrared (NIR) spectroscopy recently emerged as suitable techniques for the on-scene identification of common drugs of abuse such as cocaine, MDMA and amphetamine. This way, the overall forensic process becomes more efficient as relevant information on substance identity becomes available directly at the scene of crime. Currently, no NIR-based applications exist for the rapid, on-scene detection of NPS isomers. Herein, we present the differentiation of cathinone and phenethylamine-type NPS analogues based on their NIR spectrum recorded in 2 seconds on a portable 1350 - 2600 nm spectrometer. A prior developed data analysis model was found suitable for the identification of the methylmethcathinone (MMC) isomers 2-MMC, 3-MMC and 4-MMC. In 51 mixtures and 22 seized casework samples, the correct isomeric form was detected in all cases except for a few mixtures with an active ingredient content of 10 wt%. These results show the feasibility of on-site NPS detection as presumptive test performed directly at the scene of crime with a small size NIR-spectrometer. Additionally, in the illicit drug analysis laboratory the combination of NIR and GC-MS analysis might be suitable for robust identification of NPS isomers and analogues.

This study builds on the multicomponent analysis strategy for flash bangers which was previously introduced and where a representative sample set has been collected of a certain type of flash bangers. To expand the forensic strategy, elemental analysis of the plastic caps which are present in these items was performed. Both x-ray fluorescence (XRF) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) analysis was performed to explore the possibilities for differentiation. The inherent inhomogeneity of the plastics resulted in high variations, especially for LA-ICP-MS trace analysis. In addition, due to the lack of suitable reference materials the LA-ICP-MS results can only be used for qualitative comparisons. Although XRF is less sensitive it allows for semi-quantitative analysis and the effect of inhomogeneity is significantly reduced due to the larger sample areas. Therefore, XRF is the method of choice for elemental analysis of intact plastic caps. In this scenario initial differentiation based on visual examination is combined with elemental analysis to obtain the highest degree of discrimination. In post-explosive scenarios, using XRF is not as straightforward due the irregular shapes of the burned plastic cap residues and contamination by explosive residues. For the analysis of these post-explosive caps, LA-ICP-MS proved to be useful for characterization and differentiation. Overall, it was found that blue caps contain a considerable higher amount of elements than the white caps, mainly due to additives related to the coloring process. This limits differentiation for the flash bangers containing white caps. Therefore, isotope ratio mass spectrometry (IRMS) analysis was performed to increase the differentiation potential. Based on carbon and hydrogen isotope ratios additional sets could be distinguished, both for flash bangers containing white and blue caps, that otherwise have similar visual and elemental characteristics. With the elemental and isotopic analysis of the plastic caps, an analysis strategy has been introduced that is not based on the pyrotechnic charge and therefore provides a unique opportunity to perform characterization and differentiation of flash bangers in pre- and post-explosive casework.

To continue to assist law enforcement agencies in counteracting the illegal use of fireworks new forensic methods have to be developed. In the Netherlands, many incidents involve powerful flash bangers mainly due to irresponsible behavior and misuse for criminal activities. Obtaining tactical information for differentiation of these flash bangers is of high priority in forensic casework. A representative sample set of a certain type of flash bangers, confiscated by the Dutch police, has been collected in a time period of one year and initial characterization has been performed based on visual examination. The individual components of the flash bangers already allow for a high degree of differentiation. Ultimately, combining all visual characteristics of pyrotechnic charges, labels, fuses and caps resulted in the classification into 24 groups out of 30 seized sets of flash bangers. In addition to visual examination, this unique sample set offers a wide variety of research opportunities that could be further explored and that might prove essential in case scenarios where visual characteristics are more difficult to assess or are completely absent.

High volume screening of parcels with the aim to trace the illegal distribution and selling of fireworks using postal services is challenging. Inspection services have limited manpower and means to perform extensive visual inspection. In this study, the presence of solid pyrotechnic residues collected from cardboard shipping parcels containing fireworks was investigated for direct in-field chemical detection. Two emerging trace detection techniques, i.e., capillary electrophoresis (CE)-based inorganic oxidizer detector and infrared thermal desorption (IRTD) coupled with direct analysis in real time mass spectrometry (DART-MS) were investigated for their potential as screening tools. Detection of non-visible pyrotechnic trace residues from real-case seized parcels was demonstrated using both screening techniques. However, the high nitrate background in the commercial CE system complicated its screening for black powder traces. In addition to rapid screening, IRTD-DART-MS allowed differentiation between flash and black powder by identification of the molecular inorganic ions. Compared to the portable CE instrument, rapid screening using IRTD-DART-MS is currently limited to laboratory settings. The capabilities of these emerging techniques established solid particle and trace residue chemical detection as interesting options for parcel screening in a logistic setting.

The application of GC×GC-FID and GC×GC-MS for the chemical analysis and profiling of neat white spirit is explored and the benefit of the enhanced peak capacity offered by comprehensive two-dimensional gas chromatography is demonstrated. An extensive sampling exercise was conducted throughout The Netherlands and the production and logistics in terms of bottling and distribution of white spirits were studied. An exploratory approach based on target-peak tables and principal component analysis was employed to study the brand-to-brand differences and production variations over time. Despite the complex chemical composition of white spirit samples this study shows that chemical variation during productions is actually quite limited. Hence care has to be taken with the chemical comparison for forensic purposes. Although some clustering was noticed on brand level, the large scale production process leads to a very consistent composition across stores and brands. However, because of the broad specifications of this commodity product, substantial chemical variation was found over time. This temporal discrimination could be of forensic value when considering white spirits supplies in individual households.

Today, forensic hair analysis is considered to be a standard method for identifying chronic drug users since information about drug use stored and located in hair can cover several months to even years. When interpreting these results, one should be aware of all kind of pitfalls. External factors such as bleaching might influence the analytical result. Although the effect of hydrogen peroxide on cocaine in a solution was described before, it was never investigated whether the described reaction products (ecgonine methylester, benzoylecgonine, hydroxynorcocaine and dihydroxycocaine) are indeed found on contaminated or user hair. Since it is of great importance in forensic hair analysis to know whether cocaine and/or reaction products are detectable in hair after bleaching, matrix-assisted laser desorption/ ionization mass spectrometric imaging (MALDI-MSI) was used to study the effect of hydrogen peroxide treatment on incorporated cocaine in hairs. Cocaine oxidation products were identified in a solution based on MS/MS spectra and spatial distribution of these products in hair was explored using MALDI TOF-MS. All images were accomplished by spraying alpha-Cyano-4-hydroxycinnamic acid (CHCA) as a MALDI-matrix. Images revealed a loss of detectability of cocaine and its reaction products in hairs already after a short bleaching period. Since all compounds of interest are found in the hydrogen peroxide and wash solution, these findings indicate that all evidence of cocaine use might be lost after a hair bleaching treatment. Therefore, forensic toxicologists should take into consideration whether hair samples were bleached before making any conclusions from hair analysis results.