Etizolam, a type of anxiolytic drug, is the most commonly abused drug among hypnotic/anxiolytic medications in Japan. Although there have been reports on the postmortem identification of etizolam in the blood, the detailed distribution of etizolam among organs in an abuse case has not been reported. In this study, we examined etizolam concentrations in the blood and organs obtained from etizolam-related autopsy cases using the surrogate analyte approach (SAA) method, which can be analytically used without blank samples. Target compounds were extracted from samples using the QuEChERS method and filtrated with Captiva ND Lipids. Then, the eluates were analyzed by LC-MS/MS. Etizolam-d₃ was used as a stable isotope-labeled surrogate compound with this quantification approach. A strong linear correlation was observed for each sample, showing a correlation coefficient value at least 0.99. The right heart, left heart, and femoral vein blood etizolam concentrations ranged from 85.2 to 178.2 ng/mL, while this concentration was 592.0 ng/g in liver tissue. Here, we could determine the etizolam concentration in various autopsy samples using LC-MS/MS. In addition, this work demonstrated that the SAA method can be successfully applied to various human samples.
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http://dx.doi.org/10.1016/j.forsciint.2025.112438 | DOI Listing |
Forensic Sci Int
March 2025
Department of Legal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Chuo-ku , Hamamatsu 431-3192, Japan.
Etizolam, a type of anxiolytic drug, is the most commonly abused drug among hypnotic/anxiolytic medications in Japan. Although there have been reports on the postmortem identification of etizolam in the blood, the detailed distribution of etizolam among organs in an abuse case has not been reported. In this study, we examined etizolam concentrations in the blood and organs obtained from etizolam-related autopsy cases using the surrogate analyte approach (SAA) method, which can be analytically used without blank samples.
View Article and Find Full Text PDFMol Neurodegener
March 2025
VIB Center for Brain and Disease Research and Department of Neurosciences, KU Leuven, Louvain, Belgium.
Background: Recent studies highlight the critical role of microglia in neurodegenerative disorders, and emphasize the need for humanized models to accurately study microglial responses. Human-mouse microglia xenotransplantation models are a valuable platform for functional studies and for testing therapeutic approaches, yet currently those models are only available for academic research. This hampers their implementation for the development and testing of medication that targets human microglia.
View Article and Find Full Text PDFJ Zoo Wildl Med
March 2025
Division of Comparative Pathology, Department of Pathology & Laboratory Medicine, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Serum protein analyses are beneficial tools used to evaluate the health status of animals in a clinical veterinary setting. Capillary zone electrophoresis (CZE) is becoming more commonly used in diagnostic laboratories, and commercial reagents for the quantitation of acute phase proteins (APP) are available for validation in nondomesticated mammals. With increased numbers of red foxes () presenting to wildlife facilities with sarcoptic mange, there is a potential for a clinically impactful tool in protein electrophoresis and/or APP quantitation in this species.
View Article and Find Full Text PDFSeptoria tritici blotch (STB) is a predominant foliar disease of wheat, caused by the pathogen Zymoseptoria tritici. This disease can lead to substantial yield losses warranting control by using expensive fungicides. One effective method of STB control is the utilization of resistant wheat varieties.
View Article and Find Full Text PDFJ Parkinsons Dis
March 2025
Neurological Disorder Research Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
The accurate diagnosis of synucleinopathies-neurodegenerative diseases marked by misfolded α-synuclein protein aggregates, such as Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy-remains a critical challenge. Conventional clinical criteria, frequently verified only through postmortem examination, results in diagnostic delays that impede timely intervention. Seeding amplification assay (SAA) has emerged as a promising diagnostic tool, offering high sensitivity for detecting α-synuclein aggregates even in early disease stages.
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