Here we report the identification and quantitation of cyclopropyl-fentanyl in a fatality casework occurred due to a poly-drug toxicity in Spain in December 2017. The cyclopropyl-fentanyl was identified in non-biological (paraphernalia) and biological samples (whole-blood, vitreous humor and urine). Conventional techniques (GC-MS) and the UV-Vis spectral allowed differencing between the two structural isomer compounds of fentanyl (cyclopropyl and crotonyl) when the CRM was not available at the laboratory. Both of the drugs have the same MS spectra but different UV-Vis spectra due to the presence of an additional chromophore group in the case of crotonyl. The cyclopropyl-fentanyl detection allowed generating an alert and contributing to the surveillance and detection of this dangerous substance found mixed in doses of clandestine sale heroin. Then, high-resolution analytical techniques (LC-HRMS-MS), showed limitations for the identification of the isobaric fentanyl compounds but they had a high potential for fentanyl metabolites identification. Two tentative metabolites were identified in urine samples: cyclopropyl-norfentanyl and N-methyl cyclopropyl-norfentanyl. Finally, the systematic routine method (LC-MS-MS) was validated and applied to the quantification of cyclopropyl-fentanyl in a blood sample. A obtained value (20.4 ng/mL) was in the range of those reported in other cases in different countries (from 8 to 30 mg/ mL), being the determined concentration of cyclopropyl-fentanyl high enough to infer that this fentanyl analog had a main role as cause of death. As far as we know, this is the first fatality reported in Spain involving cyclopropyl-fentanyl.
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http://dx.doi.org/10.1093/jat/bkaa081 | DOI Listing |
Appl Spectrosc
July 2024
Department of Chemistry and Biochemistry, Florida International University, Miami, Florida, USA.
Fentanyl and fentanyl analogs are the main cause of recent overdose deaths in the United States. The presence of fentanyl analogs in illicit drugs makes it difficult to estimate their potencies. This makes the detection and differentiation of fentanyl analogs critically significant.
View Article and Find Full Text PDFDrug Alcohol Rev
March 2023
Department of Medicine, Faculty of Medicine, University of British Columbia, Vancouver, Canada.
Introduction: The emergence of fentanyl and its analogues have contributed to a drastic rise in overdose-related mortality in recent years. The objective of this study was to determine the number of drug checking samples containing fentanyl and fentanyl analogues using both point of care and confirmatory drug checking technologies.
Methods: Point-of-care drug checking data, using a combination of fentanyl immunoassay strips and Fourier-transform infrared spectroscopy (FTIR), were collected at harm reduction sites in Vancouver and Surrey, British Columbia.
Clin Mass Spectrom
November 2020
Albany Medical Center (AMC), Albany, NY, USA.
The opioid crisis is linked to an increased misuse of fentanyl as well as fentanyl analogs that originate from the illicit drug market. Much of our current understanding of fentanyl and fentanyl analog use in our communities comes from postmortem toxicology findings. In the clinical settings of addiction medicine and pain management, where the opioid abuse potential is high, the use of fentanyl, as well as specific fentanyl analogs, may be underestimated due to limited plasma testing and limited availability of assays with suitable analytical sensitivity and selectivity to detect misuse of fentanyls.
View Article and Find Full Text PDFMol Pharm
September 2020
Laboratory of Adjuvant and Antigen Research, U.S. Military HIV Research Program, Walter Reed Army Institute of Research, 503 Robert Grant Avenue, Silver Spring, Maryland 20910, United States.
Active immunization is an emerging potential modality to combat fatal overdose amid the opioid epidemic. In this study, we described the design, synthesis, formulation, and animal testing of an efficacious vaccine against fentanyl. The vaccine formulation is composed of a novel fentanyl hapten conjugated to tetanus toxoid (TT) and adjuvanted with liposomes containing monophosphoryl lipid A adsorbed on aluminum hydroxide.
View Article and Find Full Text PDFJ Anal Toxicol
December 2020
Department of Chemistry and Drugs, National Institute of Toxicology and Forensic Sciences, Las Rozas de Madrid, Madrid 28232, Spain.
Here we report the identification and quantitation of cyclopropyl-fentanyl in a fatality casework occurred due to a poly-drug toxicity in Spain in December 2017. The cyclopropyl-fentanyl was identified in non-biological (paraphernalia) and biological samples (whole-blood, vitreous humor and urine). Conventional techniques (GC-MS) and the UV-Vis spectral allowed differencing between the two structural isomer compounds of fentanyl (cyclopropyl and crotonyl) when the CRM was not available at the laboratory.
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