5F-Cumyl-PINACA in 'E-Liquids' for Electronic Cigarettes

Total Page:16

File Type:pdf, Size:1020Kb

5F-Cumyl-PINACA in 'E-Liquids' for Electronic Cigarettes 5F-cumyl-PINACA in ‘e-liquids’ for electronic cigarettes – A new type of synthetic cannabinoid in a trendy product Institute of Forensic Medicine Verena Angerer, Bjoern Moosmann, Florian Franz and Volker Auwärter Forensic Toxicology Insitute of Forensic Medicine, Forensic Toxicology, Medical Center – University of Freiburg, Germany Introduction: In recent years, e-liquids used in electronic cigarettes have become an increasingly attractive alternative to smoking tobacco. Especially among young people e-cigarettes are becoming more and more popular [1]. A new trend is the use of e-liquids containing synthetic cannabinoids instead of nicotine as active ingredients. In the frame of the EU-Projects ‘SPICE’, ‘SPICE II Plus’ and ‘SPICE Profiling’, which comprise a systematic monitoring of the online market of ‘legal highs’, e-liquids were bought from online retailers who also sell herbal blends. Product monitoring Metabolism Shop X Method Method in vivo (human): Buying cumyl-PINACA serum & urine (0.6 mg oral intake) Extraction with n-Hexane Library match in vitro: GC-MS (in-house library) 5F-cumyl-PINACA incubation 1 h, 37 °C (n = 16) cumyl-PINACA pooled human liver n = 21 microsomes LC-MS/MS analysis (pHLM) Unknown Unknown Comparison to Match (3 E-liquids) (n = 5) EDND-Database (n = 2) Results HRMS, MSn After ingestion of 0.6 mg cumyl-PINACA serum concentration 0.1 O orally, the volunteer did not experience • Elemental composition 0.08 NH any drug-related symptom. Cumyl- • Structural information 0.06 N 0.04 N PINACA itself could be detected in serum c [ng/ml] e.g. 0.02 Isolation with semi- over a period of about 17 h. The Fig 1: 0 preparative HPLC or maximum concentration observed was 0 10203040 Flash Chromatographie time [h] 5F-cumyl-PINACA 0.1 ng/ml (6 h after ingestion, Fig. 2). Pure substance F The main metabolites of cumyl-PINACA Fig.2: Serum concentration of (reference material) showed mono- and dihydroxylation at the cumyl-PINACA after 0.6 mg (oral) pentyl moiety (in-vivo and in-vitro) and Results could be detected for at least 31 h (Fig.3) 47 % of the e-liquids contained only nicotine as active ingredient. The Main metabolites of cumyl-PINACA other liquids contained one or more synthetic cannabinoids, e.g. O O O 5F-APINACA, AB-PINACA or 5F-PB-22. Three of the liquids sold as NH NH NH ‘c-liquids’ (all from one retailer) contained 5F-cumyl-PINACA (Fig. 1). N N Hydroxylation N Hydroxylation N N N in vitro + in vivo in vitro + in vivo To assess the relative potency of this new substance class – carrying M01 M07 (probably a cumyl-moiety - a set of synthetic cannabinoids (AB-CHMINACA, HO M02 HO 5-hydroxy-Pentyl) M08 M10 AB-FUBINACA, AB-PINACA, AM-2201, cumyl-PINACA, EG-018, HO JWH-018, MDMB-CHMICA, THJ-2201) were characterised using the cumyl-PINACA Oxidation Oxidation cAMP Biosensor Assay with CB1 as target (DiscoveRx, Fremont, 1.40E+07 in vitro + in vivo in vitro USA). The results of the Biosensor Assay are listed in Table 1. 1.20E+07 M07 M08 1.00E+07 O M10 NH O Assay 8.00E+06 M09 NH Compound Name EC50 (nM) Curve Top Max Response M01 Format 6.00E+06 M02 N 4.00E+06 N AB-CHMINACA Agonist 0.28 94.8 94.827 Area/Crea100 N Hydroxylation N 2.00E+06 AB-FUBINACA Agonist 0.89 97.4 97.82 0.00E+00 in vitro AB-PINACA Agonist 1.74 92.3 95.254 0.0 10.0 20.0 30.0 40.0 Time [h] AM-2201 Agonist 0.45 103 101.41 O HO Fig.3: main metabolites of cumyl- M09 Cumyl-PINACA Agonist 0.06 93.7 92.86 PINACA in urine after 0.6 mg (oral) O EG-018 Agonist 40.7 74.3 71.826 JWH-018 Agonist 1.13 97.6 97.392 Main metabolites of 5F-cumyl-PINACA (in vitro only) MDMB-CHMICA Agonist 0.14 94.8 94.57 O THJ-2201 Agonist 1.68 95.6 91.92 NH O Table.1: results of the cAMP Biosensor Assay NH N N O N NH Conclusion N N HO The increasing popularity of e-liquids particularly among young people N and the extreme potency of the added synthetic cannabinoids pose a F serious threat to public health. There is a high risk of unintended poisoning, and in the long term prevalence of these drugs could rise in F the younger population due to introduction of trendy products. 5F-cumyl-PINACA HO Acknowledgement: References: Contact: The authors would like to thank Sonja Klemenc from National Forensic Laboratory Ljubljana, Slovenia for providing [1] Camenga DR, Cavallo DA, Kong G, et al. Verena Angerer cumyl-PINACA. Adolescents' and young adults' perceptions of Institute of Forensic Medicine, Forensic Toxicology, electronic cigarettes for smoking cessation: A focus This publication has been produced with the financial support of Medical Center – University of Freiburg group study. Nicotine & tobacco research: official the European Commission (JUST/2011/ Albertstr. 9, 79104 Freiburg, Germany DPIP/AG/3597 and JUST/2013/ISEC/DRUGS/ journal of the Society for Research on Nicotine and AG/6421), the German Federal Ministry of Tobacco 2015. [email protected] Health and the City of Frankfurt/Main..
Recommended publications
  • DEPARTMENT of JUSTICE Drug Enforcement
    This document is scheduled to be published in the Federal Register on 08/03/2021 and available online at DEPARTMENT OF JUSTICEfederalregister.gov/d/2021-16499, and on govinfo.gov Drug Enforcement Administration Bulk Manufacturer of Controlled Substances Application: Cerilliant Corporation [Docket No. DEA-873] AGENCY: Drug Enforcement Administration, Justice. ACTION: Notice of application. SUMMARY: Cerilliant Corporation has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information. DATES: Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before [INSERT DATE 60 DAYS AFTER DATE OF PUBLICATION IN THE FEDERAL REGISTER]. Such persons may also file a written request for a hearing on the application on or before [INSERT DATE 60 DAYS AFTER DATE OF PUBLICATION IN THE FEDERAL REGISTER]. ADDRESS: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this is notice that on June, 24, 2021, Cerilliant Corporation, 811 Paloma Drive, Suite A, Round Rock, Texas 78665-2402, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): Controlled Substance Drug Code Schedule 3-Fluoro-N-methylcathinone
    [Show full text]
  • Analysis of Synthetic Cannabinoids and Drugs of Abuse Amongst HIV-Infected Individuals
    City University of New York (CUNY) CUNY Academic Works Student Theses John Jay College of Criminal Justice Fall 12-2016 Analysis of synthetic cannabinoids and drugs of abuse amongst HIV-infected individuals Jillian M. Wetzel CUNY John Jay College, [email protected] How does access to this work benefit ou?y Let us know! More information about this work at: https://academicworks.cuny.edu/jj_etds/2 Discover additional works at: https://academicworks.cuny.edu This work is made publicly available by the City University of New York (CUNY). Contact: [email protected] i Analysis of synthetic cannabinoids and drugs of abuse amongst HIV-infected individuals A thesis presented in partial fulfillment of the requirements for the degree of Master of Science in Forensic Science John Jay College of Criminal Justice City University of New York Jillian Wetzel December 2016 ii Analysis of synthetic cannabinoids and drugs of abuse amongst HIV-infected individuals Jillian Michele Wetzel This thesis has been presented to and accepted by the Office of Graduate Studies, John Jay College of Criminal Justice in partial fulfillment of the requirements for the degree of Master of Science in Forensic Science Thesis Committee: Thesis Advisor: Marta Concheiro-Guisan, Ph.D. Second Reader: Shu-Yuan Cheng, Ph.D. External Reader: Richard Curtis, Ph.D. iii Acknowledgements My greatest and sincerest gratitude goes towards my thesis advisor, professor, and mentor, Dr. Marta Concheiro-Guisan. You have educated me in more ways I thought possible and I am so thankful for all the experiences you have provided me with. As an educator you not only have taught me, but also have inspired me inside and outside the classroom.
    [Show full text]
  • Recommended Methods for the Identification and Analysis of Synthetic Cannabinoid Receptor Agonists in Seized Materials (Revised and Updated)
    Recommended methods for the Identification and Analysis of Synthetic Cannabinoid Receptor Agonists in Seized Materials (Revised and updated) MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES Photo credits: UNODC Photo Library; UNODC/Ioulia Kondratovitch; Alessandro Scotti. Laboratory and Scientific Section UNITED NATIONS OFFICE ON DRUGS AND CRIME Vienna Recommended Methods for the Identification and Analysis of Synthetic Cannabinoid Receptor Agonists in Seized Materials (Revised and updated) MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES UNITED NATIONS Vienna, 2020 Note Operating and experimental conditions are reproduced from the original reference materials, including unpublished methods, validated and used in selected national laboratories as per the list of references. A number of alternative conditions and substitution of named commercial products may provide comparable results in many cases, but any modification has to be validated before it is integrated into laboratory routines. Mention of names of firms and commercial products does not imply theendorsement of the United Nations. ST/NAR/48/REV.1 © United Nations, July 2020. All rights reserved, worldwide The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. This publication has not been formally edited. Publishing production: English, Publishing and Library Section, United Nations Office at Vienna. Acknowledgements The Laboratory and Scientific Services of the United Nations Office on Drugs and Crime (UNODC) (LSS, headed by Dr.
    [Show full text]
  • Synthetic Cannabinoids (60 Substances) A) Classical Cannabinoid
    Synthetic cannabinoids (60 substances) a) Classical cannabinoid OH H OH H O Common name Chemical name CAS number Molecular Formula HU-210 3-(1,1’-dimethylheptyl)-6aR,7,10,10aR-tetrahydro-1- Synonym: 112830-95-2 C H O hydroxy-6,6-dimethyl-6H-dibenzo[b,d]pyran-9-methanol 25 38 3 11-Hydroxy-Δ-8-THC-DMH b) Nonclassical cannabinoids OH OH R2 R3 R4 R1 CAS Molecular Common name Chemical name R1 R2 R3 R4 number Formula rel-2[(1 S,3 R)-3- hydroxycyclohexyl]- 5- (2- methyloctan- 2- yl) CP-47,497 70434-82-1 C H O CH H H H phenol 21 34 2 3 rel-2[(1 S,3 R)-3- hydroxycyclohexyl]- 5- (2- methylheptan- 2- yl) CP-47,497-C6 - C H O H H H H phenol 20 32 2 CP-47,497-C8 rel-2- [(1 S,3 R)-3- hydroxycyclohexyl]- 5- (2- methylnonan- 2- yl) 70434-92-3 C H O C H H H H Synonym: Cannabicyclohexanol phenol 22 36 2 2 5 CAS Molecular Common name Chemical name R1 R2 R3 R4 number Formula rel-2[(1 S,3 R)-3- hydroxycyclohexyl]- 5- (2- methyldecan- 2- yl) CP-47,497-C9 - C H O C H H H H phenol 23 38 2 3 7 rel-2- ((1 R,2 R,5 R)-5- hydroxy- 2- (3- hydroxypropyl)cyclohexyl)- 3-hydroxy CP-55,940 83003-12-7 C H O CH H H 5-(2- methyloctan- 2- yl)phenol 24 40 3 3 propyl rel-2- [(1 S,3 R)-3- hydroxy-5,5-dimethylcyclohexyl]- 5- (2- Dimethyl CP-47,497-C8 - C H O C H CH CH H methylnonan-2- yl)phenol 24 40 2 2 5 3 3 c) Aminoalkylindoles i) Naphthoylindoles 1' R R3' R2' O N CAS Molecular Common name Chemical name R1’ R2’ R3’ number Formula [1-[(1- methyl- 2- piperidinyl)methyl]- 1 H-indol- 3- yl]- 1- 1-methyl-2- AM-1220 137642-54-7 C H N O H H naphthalenyl-methanone 26 26 2 piperidinyl
    [Show full text]
  • 2 Spice English Presentation
    Spice Spice contains no compensatory substances Специи не содержит компенсационные вещества Spice is a mix of herbs (shredded plant material) and manmade chemicals with mind-altering effects. It is often called “synthetic marijuana” because some of the chemicals in it are similar to ones in marijuana; but its effects are sometimes very different from marijuana, and frequently much stronger. It is most often labeled “Not for Human Consumption” and disguised as incense. Eliminationprocess • The synthetic agonists such as THC is fat soluble. • Probably, they are stored as THC in cell membranes. • Some of the chemicals in Spice, however, attach to those receptors more strongly than THC, which could lead to a much stronger and more unpredictable effect. • Additionally, there are many chemicals that remain unidentified in products sold as Spice and it is therefore not clear how they may affect the user. • Moreover, these chemicals are often being changed as the makers of Spice alter them to avoid the products being illegal. • To dissolve the Spice crystals Acetone is used endocannabinoids synhtetic THC cannabinoids CB1 and CB2 agonister Binds to cannabinoidreceptor CB1 CB2 - In the brain -in the immune system Decreased avtivity in the cell ____________________ Maria Ellgren Since some of the compounds have a longer toxic effects compared to naturally THC, as reported: • negative effects that often occur the day after consumption, as a general hangover , but without nausea, mentally slow, confused, distracted, impairment of long and short term memory • Other reports mention the qualitative impairment of cognitive processes and emotional functioning, like all the oxygen leaves the brain.
    [Show full text]
  • How Present Synthetic Cannabinoids Can Help Predict Symptoms in the Future
    MOJ Toxicology Mini Review Open Access How present synthetic cannabinoids can help predict symptoms in the future Abstract Volume 2 Issue 1 - 2016 New synthetic cannabinoids appear regularly in the illicit drug market, often in response to Melinda Wilson-Hohler,1 Wael M Fathy,2 legal restrictions. These compounds are characterized by increasing binding affinities (Ki) 3 to CB1 and CB2 receptors. Increasing affinity to CB receptors can occur by substitution of a Ashraf Mozayani 1Consultant, The Forensic Sciences, USA halogen on the terminal position of the pentyl chain of the classical synthetic cannabinoids. 2Post-Doctoral Fellowship, Texas Southern University, USA & Fluorination of the aliphatic side chain of established cannabinoid agonists is a popular Toxicologist, Ministry of Justice, Egypt pathway of modifying existing active drugs and synthesizing novel drugs to increase 3Professor, Barbara Jordan-Mickey Leland School of Public potency. Biological impacts of these compounds that have been reported include seizures, Affairs, Texas Southern University, USA body temperature losses that may lead to cardiac distress, as well as cases reporting delirium and severe neural incapacities. These symptoms have been reported in case Correspondence: Ashraf Mozayani, Executive Director of reports with evidence that like their cannabinoid counterparts, these compounds distribute Forensic Science and Professor, Barbara Jordan-Mickey Leland post-mortem into a variety of tissues, especially adipose tissue. Researchers have detected School of Public Affairs, Texas Southern University, USA, and identified certain synthetic cannabinoid compounds on botanicals using a variety of Tel17132526556, Email [email protected] separation and detection systems such as GC-FID and GC-MS, as well as LC-MS/MS and NMR.
    [Show full text]
  • Model Scheduling New/Novel Psychoactive Substances Act (Third Edition)
    Model Scheduling New/Novel Psychoactive Substances Act (Third Edition) July 1, 2019. This project was supported by Grant No. G1799ONDCP03A, awarded by the Office of National Drug Control Policy. Points of view or opinions in this document are those of the author and do not necessarily represent the official position or policies of the Office of National Drug Control Policy or the United States Government. © 2019 NATIONAL ALLIANCE FOR MODEL STATE DRUG LAWS. This document may be reproduced for non-commercial purposes with full attribution to the National Alliance for Model State Drug Laws. Please contact NAMSDL at [email protected] or (703) 229-4954 with any questions about the Model Language. This document is intended for educational purposes only and does not constitute legal advice or opinion. Headquarters Office: NATIONAL ALLIANCE FOR MODEL STATE DRUG 1 LAWS, 1335 North Front Street, First Floor, Harrisburg, PA, 17102-2629. Model Scheduling New/Novel Psychoactive Substances Act (Third Edition)1 Table of Contents 3 Policy Statement and Background 5 Highlights 6 Section I – Short Title 6 Section II – Purpose 6 Section III – Synthetic Cannabinoids 13 Section IV – Substituted Cathinones 19 Section V – Substituted Phenethylamines 23 Section VI – N-benzyl Phenethylamine Compounds 25 Section VII – Substituted Tryptamines 28 Section VIII – Substituted Phenylcyclohexylamines 30 Section IX – Fentanyl Derivatives 39 Section X – Unclassified NPS 43 Appendix 1 Second edition published in September 2018; first edition published in 2014. Content in red bold first added in third edition. © 2019 NATIONAL ALLIANCE FOR MODEL STATE DRUG LAWS. This document may be reproduced for non-commercial purposes with full attribution to the National Alliance for Model State Drug Laws.
    [Show full text]
  • Cannabinoid-Like Effects of Five Novel Carboxamide Synthetic Cannabinoids T ⁎ Michael B
    Neurotoxicology 70 (2019) 72–79 Contents lists available at ScienceDirect Neurotoxicology journal homepage: www.elsevier.com/locate/neuro Full Length Article Cannabinoid-like effects of five novel carboxamide synthetic cannabinoids T ⁎ Michael B. Gatch , Michael J. Forster Department of Pharmacology and Neuroscience, Center for Neuroscience Discovery, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX, 76107-2699, USA ARTICLE INFO ABSTRACT Keywords: A new generation of novel cannabinoid compounds have been developed as marijuana substitutes to avoid drug Drug discrimination control laws and cannabinoid blood tests. 5F-MDMB-PINACA (also known as 5F-ADB, 5F-ADB-PINACA), MDMB- Locomotor activity CHIMICA, MDMB-FUBINACA, ADB-FUBINACA, and AMB-FUBINACA (also known as FUB-AMB, Rat MMB-FUBINACA) were tested for in vivo cannabinoid-like effects to assess their abuse liability. Locomotor Mouse activity in mice was tested to screen for locomotor depressant effects and to identify behaviorally-active dose Abuse liability ranges and times of peak effect. Discriminative stimulus effects were tested in rats trained to discriminate Δ9- tetrahydrocannabinol (3 mg/kg, 30-min pretreatment). 5F-MDMB-PINACA (ED50 = 1.1 mg/kg) and MDMB- CHIMICA (ED50 = 0.024 mg/kg) produced short-acting (30 min) depression of locomotor activity. ADB-FUBINACA (ED50 = 0.19 mg/kg), and AMB- FUBINACA (ED50 = 0.19 mg/kg) depressed locomotor activity for 60–90 min; whereas MDMB-FUBINACA (ED50 = 0.04 mg/kg) depressed locomotor activity for 150 min. AMB-FUBINACA produced tremors at the highest dose tested. 5F-MDMB-PINACA (ED50 = 0.07), MDMB- CHIMICA (ED50 = 0.01 mg/kg), MDMB-FUBINACA (ED50 = 0.051 mg/kg), ADB-FUBINACA (ED50 = 0.075 mg/ 9 kg) and AMB-FUBINACA (ED50 = 0.029) fully substituted for the discriminative stimulus effects of Δ -THC following 15-min pretreatment.
    [Show full text]
  • Alcohol and Drug Abuse Subchapter 9
    Chapter 8 – Alcohol and Drug Abuse Subchapter 9 Regulated Drug Rule 1.0 Authority This rule is established under the authority of 18 V.S.A. §§ 4201 and 4202 which authorizes the Vermont Board of Health to designate regulated drugs for the protection of public health and safety. 2.0 Purpose This rule designates drugs and other chemical substances that are illegal or judged to be potentially fatal or harmful for human consumption unless prescribed and dispensed by a professional licensed to prescribe or dispense them and used in accordance with the prescription. The rule restricts the possession of certain drugs above a specified quantity. The rule also establishes benchmark unlawful dosages for certain drugs to provide a baseline for use by prosecutors to seek enhanced penalties for possession of higher quantities of the drug in accordance with multipliers found at 18 V.S.A. § 4234. 3.0 Definitions 3.1 “Analog” means one of a group of chemical components similar in structure but different with respect to elemental composition. It can differ in one or more atoms, functional groups or substructures, which are replaced with other atoms, groups or substructures. 3.2 “Benchmark Unlawful Dosage” means the quantity of a drug commonly consumed over a twenty-four-hour period for any therapeutic purpose, as established by the manufacturer of the drug. Benchmark Unlawful dosage is not a medical or pharmacologic concept with any implication for medical practice. Instead, it is a legal concept established only for the purpose of calculating penalties for improper sale, possession, or dispensing of drugs pursuant to 18 V.S.A.
    [Show full text]
  • Alcohol and Drug Abuse Subchapter 9 Regulated Drug Rule 1.0 Authority
    Chapter 8 – Alcohol and Drug Abuse Subchapter 9 Regulated Drug Rule 1.0 Authority This rule is established under the authority of 18 V.S.A. §§ 4201 and 4202 which authorizes the Vermont Board of Health to designate regulated drugs for the protection of public health and safety. 2.0 Purpose This rule designates drugs and other chemical substances that are illegal or judged to be potentially fatal or harmful for human consumption unless prescribed and dispensed by a professional licensed to prescribe or dispense them, and used in accordance with the prescription. The rule restricts the possession of certain drugs above a specified quantity. The rule also establishes benchmark unlawful dosages for certain drugs to provide a baseline for use by prosecutors to seek enhanced penalties for possession of higher quantities of the drug in accordance with multipliers found at 18 V.S.A. § 4234. 3.0 Definitions 3.1 “Analog” means one of a group of chemical components similar in structure but different with respect to elemental composition. It can differ in one or more atoms, functional groups or substructures, which are replaced with other atoms, groups or substructures. 3.2 “Benchmark Unlawful Dosage” means the quantity of a drug commonly consumed over a twenty-four hour period for any therapeutic purpose, as established by the manufacturer of the drug. Benchmark Unlawful dosage is not a medical or pharmacologic concept with any implication for medical practice. Instead, it is a legal concept established only for the purpose of calculating penalties for improper sale, possession, or dispensing of drugs pursuant to 18 V.S.A.
    [Show full text]
  • Critical Review Report: ADB-FUBINACA
    Critical Review Report: ADB-FUBINACA Expert Committee on Drug Dependence Forty-first Meeting Geneva, 12-16 November 2018 This report contains the views of an international group of experts, and does not necessarily represent the decisions or the stated policy of the World Health Organization 41st ECDD (2018): ADB-FUBINACA © World Health Organization 2018 All rights reserved. This is an advance copy distributed to the participants of the 41st Expert Committee on Drug Dependence, before it has been formally published by the World Health Organization. The document may not be reviewed, abstracted, quoted, reproduced, transmitted, distributed, translated or adapted, in part or in whole, in any form or by any means without the permission of the World Health Organization. The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted and dashed lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. The World Health Organization does not warrant that the information contained in this publication is complete and correct and shall not be liable for any damages incurred as a result of its use.
    [Show full text]
  • Analysis of Synthetic Cannabinoids and Metabolites: Adding New Compounds to an Existing LC-MS/MS Method
    Analysis of Synthetic Cannabinoids and Metabolites: Adding New Compounds to an Existing LC-MS/MS Method By Sharon Lupo and Frances Carroll Abstract The analysis of synthetic cannabinoids and their metabolites can be a difficult and challenging task. Keeping up with the ever-growing list of synthetic cannabinoids that illicit drugmakers produce further complicates the analysis. As shown here, the retention and selec- tivity of the Raptor Biphenyl column allow new drugs to be added to an existing method, providing labs with an important vehicle for improving efficiency and productivity. Introduction The analysis of synthetic cannabinoids and their metabolites has become a routine procedure in many forensic toxicology laborato- ries as new drugs appear on the market. When developing methods for these compounds, optimization of analysis time, resolution between metabolites, method robustness, and the ability to add emerging compounds are of ultimate importance as they influence method effectiveness and longevity. Because the Raptor Biphenyl column combines the speed of superficially porous particles (SPP) with the resolution of highly selective USLC technology, we chose it when developing a simple dilute-and-shoot method that included both synthetic cannabinoids and their metabolites in urine. Our original work produced a fast method that separated 29 target compounds in less than seven minutes. When analyzing synthetic cannabinoids, chromatographic resolution of some target compounds that cannot be determined by MS alone is essential. For example, synthetic cannabinoids JWH-018 and JWH-073 and their metabolites must be separated chro- matographically due to the presence of multiple positional isomers among the monohydroxylated metabolites. These isomers form because each parent compound has multiple sites available for hydroxylation (Figure 1).
    [Show full text]