Abuse of Xylazine by Human and its Emerging Problems: A Review from Forensic Perspective

@#Xylazine is a sedative, analgesic and muscle relaxant widely applied in the veterinary field. However, owing to its depressant effect, xylazine has become a substance of abuse by humans. Misuse of xylazine not only triggers unwanted consequences (death), but also linked with various crimes. Google Scholar, PubMed and SciFinder were used to retrieve articles and case reports in relation to the misuses of xylazine and established analytical methods for forensic investigation until November 2021. Literatures reported the accidental and intended poisoning of xylazine, recreational use of xylazine and as an adulterant in recreational drugs. In addition to being a facilitator of crime and sexual assault, it is administered illegally to food producing animals as a sedative and to sports animals as a doping agent. Problems associated with the abuse of xylazine were highlighted in this review, covering the unknown prevalence of xylazine abuse and the need to revise the regulatory status of xylazine. In addition, limited screening and confirmatory methods that can be readily utilised to detect xylazine either alone or simultaneously with other substances of abuse, particularly useful for forensic toxicology and narcotic section were available in the literature. As a conventionally used veterinary drug, xylazine is undoubtedly a potentially hazardous drug, and the investigations on its potential abuse would enhance routine forensic examination to keep pace with the status of illicit drugs.

Validación de un método rápido en orina por lC/MS/MS para la búsqueda de compuestos empleados en sumisión química y su aplicación a muestras reales / Validation of a fast screening method in urine by lC/MS/MS for compounds used in drug-facilitated crime (DFC) and its application to real samples

La Oficina de Naciones Unidas contra la Droga y el Delito (UNODC) en 2011 señala que "El delito facilitado por drogas (DFD) es una expresión general que abarca la violación y otras agresiones sexuales, el robo con violencia o intimidación, la extorsión de dinero y los malos tratos deliberados de ancianos o niños bajo la influencia de sustancias sicotrópicas". En este trabajo se validó un método cualitativo y rápido a partir de muestras de orina por LC/MS/MS para 39 compuestos comprendidos en los listados de sumisión química. El objetivo fue alcanzar un límite de detección un 50 % por debajo de la concentración propuesta como "Límites mínimos de funcionamiento exigidos (MRPL)" por la UNODC, para poder ser aplicado a muestras reales.

The United Nations Office on Drugs and Crime (UNODC) in 2011, states that "The Drug-facilitated crime (DFC) is a general term that includes rape or other sexual assault, robbery, money extortion, as well as the deliberate maltreatment of the elderly or children under the influence of psychotropic substances". In this work we validated a qualitative and fast method from urine samples by LC/MS/MS for 39 compounds included in the Drug-facilitated crime lists. The aim was to reach a detection limit of 50% below the proposed concentration as "minimum required performance limits (MRPL)" by UNODC in order to be applied in real samples.

Desenvolvimento de métodos analíticos para a identificação de drogas facilitadoras de crime em amostras de urina / Developing analytical methods for identification of drug-facilitated crime in urine samples

As drogas facilitadoras de crime (DFC) são uma série de substâncias químicas que permitem o ato sexual e/ou roubo com pouca ou nenhuma resistência da vítima. Benzodiazepínicos, gama-hidroxibutirato (GHB), cetamina e etanol são clássicas DFC, porém outras substâncias também têm sido utilizadas. Devido às diferentes classes de DFC e a necessidade de métodos sensíveis, a determinação dessas substâncias é um desafio aos toxicologistas forenses. A proposta do estudo foi desenvolver métodos analíticos para determinação principais analitos alvos de DFC para benzodiazepínicos, cetamina e GHB em amostras de urina. Esta matriz biológica é considerada uma amostra não-invasiva e apresenta um período de detecção maior que o sangue. A preparação das amostras foi avaliada através de microextração em fase líquida (LPME) e extração líquido-líquido (LLE). A LPME é uma técnica de extração de drogas que utiliza menor quantidade de solventes orgânicos, maior praticidade e possibilidade de obtenção de altos valores de recuperação. Os analitos foram determinados por cromatografia gasosa acoplada à espectrometria de massas (GC-MS). A LPME validada para benzodiazepínicos e seus produtos de biotransformação exigiu uma combinação de solventes e dupla derivatização para atingir a sensibilidade exigida, enquanto o método para determinação de cetamina, norcetamina e deidronorcetamina utilizou óleo essencial de eucalipto como meio extrator, caracterizando-se um procedimento ecologicamente correto com alta sensibilidade. A extração de GHB foi efetiva por LLE com redução da quantidade de solvente e tempo de análise sem o prejuízo na sensibilidade. Em geral, os métodos desenvolvidos neste trabalho são sensíveis e confiáveis para todos os analitos relatados e conclui-se que a LPME é uma técnica de preparo de amostra eficiente, versátil de baixo custo. Estas condições permitem que sua implementação em qualquer laboratório de análises toxicológicas, podendo ser aplicada em situações de DFC ou de qualquer outra natureza

Drug-facilitated crime (DFC) are a series of chemicals that allow the sexual act and/or theft with little or no resistance from the victim. Benzodiazepines, gamma-hydroxybutyrate (GHB) and ketamine and ethanol are considered classic DFC, however other substances were also used as the DFC. Due to the different classes of DFC and the need for sensitive methods, the determination of these substances is a challenge to forensic toxicologists. The purpose of this study was to develop analytical methods for determination of the main target analytes of DFC for benzodiazepines, ketamine and GHB in urine samples. This biological matrix is considered a non-invasive sample and shows a larger window of detection than blood. Sample preparation was assessed using liquid phase microextraction (LPME) and liquid-liquid extraction (LLE). The LPME is a drug extraction technique that uses less organic solvents, greater practicality and possibility of obtaining high recovery values. The analytes were determined by gas chromatography - mass spectrometry (GC-MS). The validated LPME technique for benzodiazepines and their metabolites required a combination of solvents and double derivatization to achieve the required sensitivity, while the ketamine, norketamine and dehydronorketamine method used essential oil of eucalyptus as solvent, characterizing a green chemistry approach with high sensitivity. The extraction of GHB was effective by LLE with a reduced amount of solvent and the analysis time without loss in sensitivity. In general, the methods developed in this work using GC-MS are sensitive and reliable for all analytes reported and LPME technique showed to be an efficient sample preparation, versatile and low cost. These conditions allow LPME implementation in any laboratory of toxicological analysis and it can be applied in situations of DFC or any other kind of analysis