Márcio Talhavini

Inkjet Printing of Lanthanide–Organic Frameworks for Anti-Counterfeiting Applications

Photoluminescent lanthanide-organic frameworks (Ln-MOFs) were printed onto plastic and paper foils with a conventional inkjet printer. Ln-MOF inks were used to reproduce color images that can only be observed under UV light irradiation. This approach opens a new window for exploring Ln-MOF materials in technological applications, such as optical devices (e.g., lab-on-a-chip), as proof of authenticity for official documents.

Discrimination of whisky brands and counterfeit identification by UV–Vis spectroscopy and multivariate data analysis

The discrimination of whisky brands and counterfeit identification were performed by UV-Vis spectroscopy combined with partial least squares for discriminant analysis (PLS-DA). In the proposed method all spectra were obtained with no sample preparation. The discrimination models were built with the employment of seven whisky brands: Red Label, Black Label, White Horse, Chivas Regal (12years), Ballantines Finest, Old Parr and Natu Nobilis. The method was validated with an independent test set of authentic samples belonging to the seven selected brands and another eleven brands not included in the training samples. Furthermore, seventy-three counterfeit samples were also used to validate the method. Results showed correct classification rates for genuine and false samples over 98.6% and 93.1%, respectively, indicating that the method can be helpful for the forensic analysis of whisky samples.

Discrimination and quantification of cocaine and adulterants in seized drug samples by infrared spectroscopy and PLSR

Middle infrared spectroscopy and multivariate analysis have been applied for the development of methods to perform both quantitative and qualitative analysis of real drug samples seized by the Brazilian Police Federal (BPF). Currently, quantification of cocaine and determination of adulterants in seizures is performed using gas chromatography with flame ionization detection. However, this technique requires a relatively complex sample preparation, higher time of analysis, the destruction of sample and a high cost. In this context, this paper presents a simpler method to quantify cocaine and its major adulterants in seized materials. Out of 375 seizures, taken within a time frame of 2009-2013. A total of 1085 samples were analyzed of which 500 were selected for the calibration set and 585 for the validation set. Cocaine concentration in seized samples was determined by using middle infrared spectroscopy and partial least squares regression (PLSR), obtaining an average prediction error of 3.0% (w/w), precision of 2.0 and 11.8% (w/w) of minimum detectable cocaine concentration in a range varying from 24.2 to 99.9% (w/w). Results indicate that the developed method is able to discriminate between cocaine hydrochloride and free base samples, to quantify cocaine content as well as to estimate the concentration of main adulterants phenacetin, benzocaine, caffeine, lidocaine and aminopyrine.

Classification of Brazilian and foreign gasolines adulterated with alcohol using infrared spectroscopy

The smuggling of products across the border regions of many countries is a practice to be fought. Brazilian authorities are increasingly worried about the illicit trade of fuels along the frontiers of the country. In order to confirm this as a crime, the Federal Police must have a means of identifying the origin of the fuel. This work describes the development of a rapid and nondestructive methodology to classify gasoline as to its origin (Brazil, Venezuela and Peru), using infrared spectroscopy and multivariate classification. Partial Least Squares Discriminant Analysis (PLS-DA) and Soft Independent Modeling Class Analogy (SIMCA) models were built. Direct standardization (DS) was employed aiming to standardize the spectra obtained in different laboratories of the border units of the Federal Police. Two approaches were considered in this work: (1) local and (2) global classification models. When using Approach 1, the PLS-DA achieved 100% correct classification, and the deviation of the predicted values for the secondary instrument considerably decreased after performing DS. In this case, SIMCA models were not efficient in the classification, even after standardization. Using a global model (Approach 2), both PLS-DA and SIMCA techniques were effective after performing DS. Considering that real situations may involve questioned samples from other nations (such as Peru), the SIMCA method developed according to Approach 2 is a more adequate, since the sample will be classified neither as Brazil nor Venezuelan. This methodology could be applied to other forensic problems involving the chemical classification of a product, provided that a specific modeling is performed.

Quantification of cocaine hydrochloride in seized drug samples by infrared spectroscopy and PLSR

The determination of cocaine in drug samples is an important task for law enforcement agencies such as the Brazilian Federal Police (BFP). In this sense, this paper proposes a method based on infrared spectra obtained by attenuated total reflectance (ATR) and partial least squares regression (PLSR) to quantify cocaine hydrochloride in drug samples. The method was developed and validated with 275 actual samples of drugs seized by the BFP. The determination was performed between 35 to 99% (m/m) of cocaine in the drug samples. Results indicate that the method is able to directly analyze drug samples containing cocaine in its hydrochloride form without any sample preparation with average prediction errors of 3.00% (m/m), 1.50% (m/m) precision and 13% (m/m) of minimum detectable concentration.

Discrimination of black pen inks on writing documents using visible reflectance spectroscopy and PLS-DA

The analysis of inks is performed to verify the occurrence of forgery in documents. Spectroscopic methods are attractive techniques for use in forensic document analysis as they, in most instances, preserve the integrity of the document. In this work, it is proposed a discrimination method of black pen inks of different types, brands and models for application in cursive handwriting. The visible reflectance spectra was obtained by the video spectral comparator VSC®6000 and discrimination analysis performed by partial least squares (PLS-DA). The method was validated with an independent test set and with a blind test. The bias in the results was corrected for the outlier identification. The PLS-DA models presented low root mean squared error of predictions (RMSEPs) and allowed a fast, non-destructive and an efficient discrimination of all pen inks evaluated. The method has proved to be accurate and robust regarding the handwriting of different individuals and capable of identifying the pen type, brand and pen model in a forensic case.

Application of the Metal–Organic Framework [Eu(BTC)] as a Luminescent Marker for Gunshot Residues: A Synthesis, Characterization, and Toxicity Study

The 3D metal-organic framework (MOF) [Eu(BTC)] (where BTC = trimesic acid) was synthesized in 20 min by a microwave-assisted hydrothermal method with a yield of 89%. A structural and spectroscopic study, performed by X-ray diffraction, thermogravimetry, and photoluminescence spectroscopy, showed that this framework has high crystallinity, thermal stability, and luminescence. This MOF had a red-orange luminescence when excited with ultraviolet (UV) radiation (λ = 254 nm) and a high potential for use as a luminescent marker for gunshot residues (GSR). When added to 9 mm nontoxic ammunition, it greatly improved quality of the crime scene investigation, allowing for direct visualization of the luminescent GSR on the shooters hand and firearm and at the firing range using only a portable UV lamp. The marked luminescent GSR was easily collected and characterized by nondestructive techniques, including with a Video Spectral Comparator and scanning electron microscopy/energy-dispersive spectroscopy, wherein the presence of Eu3+ ions was confirmed. Furthermore, the oral acute toxicity of this MOF was assessed in adult female Wistar rats using the Organisation for Economic Cooperation and Development 423 guidelines. This study classified the MOF [Eu(BTC)] in a less toxic Globally Harmonized System category (category 5), with a LD50 (lethal dose) of 5000 mg/kg, ensuring a wide security range for its application.

Detection of Counterfeit Durateston® Using Fourier Transform Infrared Spectroscopy and Partial Least Squares - Discriminant Analysis

Medicines containing anabolic steroids are one of the main targets for counterfeiting worldwide, including Brazil. The aim of this work was to propose a method for discriminating original and counterfeit Durateston® ampoules by Fourier transform infrared spectroscopy (FTIR) followed by chemometric analysis. Ninety-six ampoules of Durateston®, 49 originals and 47 counterfeits, were analyzed by gas chromatography with mass spectrometry (GC-MS) and by FTIR. Principal component analysis was applied to the infrared spectra to detected different clusters, corresponding to original samples and different types of counterfeits. A partial least squares - discriminant analysis method was proposed to discriminate original samples from those counterfeits that were indistinguishable from the originals in the infrared analysis. A training subset comprised of one-third of the available spectra was used to establish a suitable model that correctly discriminated all samples in the test subset, resulting in 0% of false positive or negative results and 100% of efficiency rate, sensitivity and specificity. In addition to the low cost of the infrared technique, the proposed method is fast, reliable and suitable to replace GC-MS methods used in Durateston® ampoule analyses to detect counterfeiting.

NIR hyperspectral images for identification of gunshot residue from tagged ammunition

Analysis of gunshot residues (GSR) is a vital point of interest in forensic chemistry. GSR analysis is very well established, but there is still a lack of methodology to identify GSR obtained from lead-free or ‘non-toxic ammunition’ (NTA). To identify GSR from NTA, we have proposed the incorporation of luminescent markers to provide an optical and chemical signature to GSR. Furthermore, the luminescent markers can open up prospectives for ammunition encoding by adjusting their composition. Herein, we report the distinction among GSR particles containing different MOF-based markers by analyzing their organic fractions using near-infrared hyperspectral imaging (NIR-HSI) together with multivariate analysis (MCR-ALS). The method has been proven to be effective, non-destructive and fast in distinguishing marked GSR. It is possible to detect and correctly identify 72.2% of the samples, and all cases of misclassification are related to slight amount of material collected (8.3%) or confusion caused by one of the markers (19.4%). The study is developed in a forensic context of GSR analysis; however, the methodology described here is excellent and can be extrapolated to other applications that require distinguishing MOFs with different ligands.

Identification of ANFO: Use of luminescent taggants in post-blast residues

This work describes the incorporation of luminescent taggants in cartridges of ammonium nitrate-fuel oil (ANFO) to allow easy identification and collection of post-blast residues. Metal-Organic Frameworks taggants proved to be appropriate for explosive marking when ANFO proportions were above 3.0wt.%. Lanthanide-based light emission enabled in situ retrieval of explosive residues as well as chemical identification, allowing the creation of a coding system using Energy Dispersive Spectroscopy (EDS). The proposed method will accelerate laboratory analysis and support forensic investigations, connecting evidence to suspects and/or to the explosive origin.