Exploring Methamphetamine Trends in Europe (PDF)
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Neurotransmitter Resource Guide
NEUROTRANSMITTER RESOURCE GUIDE Science + Insight doctorsdata.com Doctor’s Data, Inc. Neurotransmitter RESOURCE GUIDE Table of Contents Sample Report Sample Report ........................................................................................................................................................................... 1 Analyte Considerations Phenylethylamine (B-phenylethylamine or PEA) ................................................................................................. 1 Tyrosine .......................................................................................................................................................................................... 3 Tyramine ........................................................................................................................................................................................4 Dopamine .....................................................................................................................................................................................6 3, 4-Dihydroxyphenylacetic Acid (DOPAC) ............................................................................................................... 7 3-Methoxytyramine (3-MT) ............................................................................................................................................... 9 Norepinephrine ........................................................................................................................................................................ -
Methylphenidate Hydrochloride
Application for Inclusion to the 22nd Expert Committee on the Selection and Use of Essential Medicines: METHYLPHENIDATE HYDROCHLORIDE December 7, 2018 Submitted by: Patricia Moscibrodzki, M.P.H., and Craig L. Katz, M.D. The Icahn School of Medicine at Mount Sinai Graduate Program in Public Health New York NY, United States Contact: [email protected] TABLE OF CONTENTS Page 3 Summary Statement Page 4 Focal Point Person in WHO Page 5 Name of Organizations Consulted Page 6 International Nonproprietary Name Page 7 Formulations Proposed for Inclusion Page 8 International Availability Page 10 Listing Requested Page 11 Public Health Relevance Page 13 Treatment Details Page 19 Comparative Effectiveness Page 29 Comparative Safety Page 41 Comparative Cost and Cost-Effectiveness Page 45 Regulatory Status Page 48 Pharmacoepial Standards Page 49 Text for the WHO Model Formulary Page 52 References Page 61 Appendix – Letters of Support 2 1. Summary Statement of the Proposal for Inclusion of Methylphenidate Methylphenidate (MPH), a central nervous system (CNS) stimulant, of the phenethylamine class, is proposed for inclusion in the WHO Model List of Essential Medications (EML) & the Model List of Essential Medications for Children (EMLc) for treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) under ICD-11, 6C9Z mental, behavioral or neurodevelopmental disorder, disruptive behavior or dissocial disorders. To date, the list of essential medications does not include stimulants, which play a critical role in the treatment of psychotic disorders. Methylphenidate is proposed for inclusion on the complimentary list for both children and adults. This application provides a systematic review of the use, efficacy, safety, availability, and cost-effectiveness of methylphenidate compared with other stimulant (first-line) and non-stimulant (second-line) medications. -
21 Triglav Trophy ANNOUNCEMENT
SLOVENE SKATING UNION FIGURE SKATING CLUB JESENICE Slovene Skating Union Figure Skating Club Jesenice e-mail: [email protected] e-mail: [email protected] 21st Triglav Trophy INTERNATIONAL FIGURE SKATING COMPETITION JESENICE, SLOVENIA, April 4th–8th, 2012 ANNOUNCEMENT Organizer: Figure Skating Club Jesenice Slovene Skating Union Ledarska 4, 4270 Jesenice Celovška 25, 1000 Ljubljana Slovenia Slovenia Venue: “Podmežakla” Ice Rink, Jesenice (indoor ice rink, size 30m x 60m) Time: April 4st- April 8th, 2012 Events: SINGLE SKATING: SENIOR – Ladies, Men JUNIOR – Ladies, Men ADVANCED NOVICE – Girls, Boys _________________________________________________________________ General note: The competition will be held in accordance with the ISU Regulations figure Skating 2010 and respective ISU Communications for Figure Skating. Competition will fulfil also Communication N. 1460 paragraph 2. - ISU World Standings. TRIGLAV TROPHY 2012 1 ANNOUNCEMENT SLOVENE SKATING UNION FIGURE SKATING CLUB JESENICE Technical panel will be from (3) different ISU countries. If there are minimum 8 single skaters out of four different ISU countries, points for World Standings will be awarded. Participation: ISU Members Each team may enter four competitors (two ladies, two men) in senior single skating events and four competitors (two ladies, two men) in each category in single skating of junior and novice events (unless the Organizing Committee decides otherwise). The entries that were placed the first three at the ISU Junior Grand Prix Final 2011/2012 and ISU Grand Prix Final 2011/2012 and the medallists of the World Junior Championships 2012, Europe and World Championships 2012, are not counted into the quota above. The Slovene Skating Union and the organiser reserve the right to enter additional teams and additional competitors in each category. -
Comparison of the Characteristic Mass Fragmentations of Phenethylamines and Tryptamines by Electron Ionization Gas Chromatograph
applied sciences Article Comparison of the Characteristic Mass Fragmentations of Phenethylamines and Tryptamines by Electron Ionization Gas Chromatography Mass Spectrometry, Electrospray and Matrix-Assisted Laser Desorption Ionization Mass Spectrometry Bo-Hong Chen, Ju-Tsung Liu, Hung-Ming Chen, Wen-Xiong Chen and Cheng-Huang Lin * Department of Chemistry, National Taiwan Normal University, 88 Sec. 4 Tingchow Road, Taipei 11677, Taiwan; [email protected] (B.-H.C.); [email protected] (J.-T.L.); [email protected] (H.-M.C.); [email protected] (W.-X.C.) * Correspondence: [email protected]; Tel.: +886-2-7734-6170; Fax: +886-2-2932-4249 Received: 18 April 2018; Accepted: 19 June 2018; Published: 22 June 2018 Abstract: Characteristic mass fragmentation of 20 phenethylamine/tryptamine standards were investigated and compared by means of matrix assisted laser desorption/time-of-flight mass spectrometry (MALDI/TOFM), gas chromatography–electron ionization–mass spectrometry (GC-EI/MS) and liquid chromatography–electrospray ionization/mass spectrometry (LC-ESI/MS) + methods. As a result, three characteristic peaks ([M] and fragments from the Cβ-Cα bond breakage) were found to be unique and contained information useful in identifying 2C series compounds based on the GC-EI/MS method. We found that the protonated molecular ion ([M+H]+) and two types of fragments produced from the α-cleavage and β-cleavage processes were useful mass spectral information in the rapid screening and confirmation of phenethylamine and tryptamine derivatives when ESI/MS and MALDI/TOFMS methods were applied. This assay was successfully used to determine samples that contain illicit drugs. Keywords: phenethylamine; tryptamine; MALDI/TOFMS; GC-EI/MS; LC-ESI/MS 1. -
Pharmacology and Toxicology of Amphetamine and Related Designer Drugs
Pharmacology and Toxicology of Amphetamine and Related Designer Drugs U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES • Public Health Service • Alcohol Drug Abuse and Mental Health Administration Pharmacology and Toxicology of Amphetamine and Related Designer Drugs Editors: Khursheed Asghar, Ph.D. Division of Preclinical Research National Institute on Drug Abuse Errol De Souza, Ph.D. Addiction Research Center National Institute on Drug Abuse NIDA Research Monograph 94 1989 U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Alcohol, Drug Abuse, and Mental Health Administration National Institute on Drug Abuse 5600 Fishers Lane Rockville, MD 20857 For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, DC 20402 Pharmacology and Toxicology of Amphetamine and Related Designer Drugs ACKNOWLEDGMENT This monograph is based upon papers and discussion from a technical review on pharmacology and toxicology of amphetamine and related designer drugs that took place on August 2 through 4, 1988, in Bethesda, MD. The review meeting was sponsored by the Biomedical Branch, Division of Preclinical Research, and the Addiction Research Center, National Institute on Drug Abuse. COPYRIGHT STATUS The National Institute on Drug Abuse has obtained permission from the copyright holders to reproduce certain previously published material as noted in the text. Further reproduction of this copyrighted material is permitted only as part of a reprinting of the entire publication or chapter. For any other use, the copyright holder’s permission is required. All other matieral in this volume except quoted passages from copyrighted sources is in the public domain and may be used or reproduced without permission from the Institute or the authors. -
N-Alkylation of Phenethylamine and Tryptamine Gerta Cami-Kobeci, Paul A
Bioorganic & Medicinal Chemistry Letters 15 (2005) 535–537 N-Alkylation of phenethylamine and tryptamine Gerta Cami-Kobeci, Paul A. Slatford, Michael K. Whittlesey and Jonathan M. J. Williams* Department of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK Received 28 October 2004; revised 17 November 2004; accepted 18 November 2004 Available online 24 December 2004 Abstract—A clean and efficient method for the N-alkylation of tryptamine and phenethylamine, employing alcohols as the alkyl- ating agents, has been developed. The reaction proceeds via catalytic electronic activation, involving an iridium catalyst which activates the alcohol by borrowing hydrogen from the substrate, returning it later in the catalytic cycle. Some examples of N-heterocyclisation have been performed employing a diol as the substrate. Ó 2004 Elsevier Ltd. All rights reserved. The ability to prepare a large number of synthetically NMe2 useful and pharmacologically active compounds, either H N OH by traditional or high throughput methods, is becoming Me S O O HN increasingly important. Herein we report an efficient, N atom economic, one-pot method for the N-alkylation H of tryptamine and phenethylamine, giving water as the OH only by-product. Sumatriptan Nylidrin Figure 1. The tryptamine sub-structure is present in numerous naturally occurring and synthetic compounds, many of which exhibit important pharmacological activity. For mercially available iminophosphorane 3.5 The reaction example, a number of 5-alkyltryptamine derivatives proceeds via a strategy -
Detection of Phenethylamine, Amphetamine, and Tryptamine Imine By-Products from an Acetone Extraction
Detection of Phenethylamine, Amphetamine, and Tryptamine Imine By-Products from an Acetone Extraction Mary A. Yohannan* and Arthur Berrier U.S. Department of Justice Drug Enforcement Administration Special Testing and Research Laboratory 22624 Dulles Summit Court Dulles, VA 20166 [email: mary.a.yohannan -at- usdoj.gov] ABSTRACT: The formation of imine by-products from phenethylamines, amphetamines, and tryptamines upon an acetone extraction is presented. These imine by-products were characterized using GC/MSD and exhibited preferential cleavage at the α-carbon of the alkyl chain. Further characterization of the imine by-products of phenethylamine and tryptamine was done using IR and NMR. KEYWORDS: phenethylamine, tryptamine, imine, acetone, schiff base, drug chemistry, forensic chemistry In most forensic laboratories, the solvents used to extract at the α-carbon on the alkyl chain. In addition to GC/MS, the drugs are chosen based upon their solubility properties and their imines formed from phenethylamine base and tryptamine base ability to not interact with the drug. In fact, there are very few were characterized by Fourier transform-infrared spectroscopy publications where a solvent used to extract a drug reacts with (FTIR) and nuclear magnetic resonance (NMR) spectroscopy. the drug and forms by-products [1-3]. This laboratory recently discovered that an additional Experimental component was formed when acetone was used to extract a Solvents, Chemicals, and Materials sample containing a known tryptamine. Analysis by gas Acetone was ACS/HPLC grade from Burdick and Jackson chromatography/mass spectroscopy (GC/MS) of the acetone Laboratories (Muskegon, MI). Phenethylamine base and extract yielded an extra peak in the total ion chromatogram that tryptamine base were obtained from Sigma-Aldrich Chemicals was approximately half the abundance of the known tryptamine (Milwaukee, WI). -
Recommended Methods for the Identification and Analysis Of
Vienna International Centre, P.O. Box 500, 1400 Vienna, Austria Tel: (+43-1) 26060-0, Fax: (+43-1) 26060-5866, www.unodc.org RECOMMENDED METHODS FOR THE IDENTIFICATION AND ANALYSIS OF AMPHETAMINE, METHAMPHETAMINE AND THEIR RING-SUBSTITUTED ANALOGUES IN SEIZED MATERIALS (revised and updated) MANUAL FOR USE BY NATIONAL DRUG TESTING LABORATORIES Laboratory and Scientific Section United Nations Office on Drugs and Crime Vienna RECOMMENDED METHODS FOR THE IDENTIFICATION AND ANALYSIS OF AMPHETAMINE, METHAMPHETAMINE AND THEIR RING-SUBSTITUTED ANALOGUES IN SEIZED MATERIALS (revised and updated) MANUAL FOR USE BY NATIONAL DRUG TESTING LABORATORIES UNITED NATIONS New York, 2006 Note Mention of company names and commercial products does not imply the endorse- ment of the United Nations. This publication has not been formally edited. ST/NAR/34 UNITED NATIONS PUBLICATION Sales No. E.06.XI.1 ISBN 92-1-148208-9 Acknowledgements UNODC’s Laboratory and Scientific Section wishes to express its thanks to the experts who participated in the Consultative Meeting on “The Review of Methods for the Identification and Analysis of Amphetamine-type Stimulants (ATS) and Their Ring-substituted Analogues in Seized Material” for their contribution to the contents of this manual. Ms. Rosa Alis Rodríguez, Laboratorio de Drogas y Sanidad de Baleares, Palma de Mallorca, Spain Dr. Hans Bergkvist, SKL—National Laboratory of Forensic Science, Linköping, Sweden Ms. Warank Boonchuay, Division of Narcotics Analysis, Department of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand Dr. Rainer Dahlenburg, Bundeskriminalamt/KT34, Wiesbaden, Germany Mr. Adrian V. Kemmenoe, The Forensic Science Service, Birmingham Laboratory, Birmingham, United Kingdom Dr. Tohru Kishi, National Research Institute of Police Science, Chiba, Japan Dr. -
Euro Changeover-Related Inflation in Estonia
WORKING PAPER SERIES NO 1732 / SEPTEMBER 2014 ONE CURRENCY, ONE PRICE? EURO CHANGEOVER-RELATED INFLATION IN ESTONIA Jaanika Meriküll and Tairi Rõõm GROCERY PRICES IN THE EURO AREA: FINDINGS FROM INFORMAL ESCB EXPERT GROUP SET-UP TO ANALYSE A DISAGGREGATED PRICE DATASET In 2014 all ECB publications feature a motif taken from the €20 banknote. NOTE: This Working Paper should not be reported as representing the views of the European Central Bank (ECB). The views expressed are those of the authors and do not necessarily refl ect those of the ECB. Grocery prices in the euro area: Findings from informal ESCN expert group to analsyse a disaggregated price dataset This paper was prepared as part of a Eurosystem project group established to analyse a large-scale disaggregated dataset on grocery prices in the euro area. This proprietary dataset was obtained as a follow up to the 2011 Eurosystem Structural Issues Report (SIR) entitled “Structural features of the distributive trades and their impact on prices in the euro area”. The main motivation for obtaining these data was to enable the analysis of a variety of issues that was previously not possible owing to data limitations. More specifi cally (i) analysis of Single Market issues and quantifi cation of border effects (ii) measuring the impact of competition – both at the producer and retail level – on consumer price levels and (iii) consider potential implications for infl ation measurement arising from structural changes in retail sector such as the growing importance of discounters and private label brands. The data were obtained from Nielsen, an international market information and measurement company. -
Beta-Phenylethylamine, a Small Molecule with a Large Impact
Article ID: WMC004459 ISSN 2046-1690 Beta-phenylethylamine, a small molecule with a large impact Peer review status: Yes Corresponding Author: Ms. Meredith Irsfeld, Fargo, North Dakota State University - United States of America Submitting Author: Dr. Birgit Pruess, Associate Professor, North Dakota State University, Fargo ND 58108, 58108 - United States of America Other Authors: Mr. Matthew Spadafore, Fargo, North Dakota State University - United States of America Previous Article Reference: http://www.webmedcentral.com/article_view/4409 Article ID: WMC004459 Article Type: Review articles Submitted on:12-Dec-2013, 07:13:25 PM GMT Published on: 13-Dec-2013, 06:22:50 AM GMT Article URL: http://www.webmedcentral.com/article_view/4459 Subject Categories:BIOCHEMISTRY Keywords:neurotransmitter, antimicrobial, food spoilage How to cite the article:Irsfeld M, Spadafore M, Pruess B. Beta-phenylethylamine, a small molecule with a large impact. WebmedCentral BIOCHEMISTRY 2013;4(12):WMC004459 Copyright: This is an open-access article distributed under the terms of the Creative Commons Attribution License(CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Source(s) of Funding: 1R15AI089403 from NIH/NIAID Competing Interests: The authors declare no competing interets. WebmedCentral > Review articles Page 1 of 16 WMC004459 Downloaded from http://www.webmedcentral.com on 13-Dec-2013, 10:11:14 AM Beta-phenylethylamine, a small molecule with a large impact Author(s): Irsfeld M, Spadafore M, Pruess B Abstract functional relatives of biogenic amines, we present information on other trace amines and biogenic amines as appropriate. General information about PEA is summarized in Chapter I, including the During a screen of bacterial nutrients as inhibitors of chemical properties of PEA (1.1), its natural Escherichia coli O157:H7 biofilm, the Prub research occurrence and biological synthesis (1.2), and its team made an intriguing observation: among 95 chemical synthesis (1.3). -
Adapting to Change UK Policy Towards the Arctic Polar Regions Department Foreign and Commonwealth Office, King Charles Street, London SW1A 2AH
Adapting To Change UK policy towards the Arctic Polar Regions Department Foreign and Commonwealth Office, King Charles Street, London SW1A 2AH © Crown copyright 2013. You may re-use this information (not Any enquiries regarding this including logos) free of charge in any publication should be sent to us format or medium, under the terms of at [email protected]. the Open Government Licence. To view this licence, visit www. This publication is available for download nationalarchives.gov.uk/doc/ at www.official-documents.gov.uk. opengovernment-licence/ or write to the Information Policy Team, The National Archives, Kew, London TW9 4DU,or email: [email protected]. Adapting To Change UK policy towards the Arctic i - Adapting To Change - UK policy towards the Arctic Mark Simmonds Minister for the Polar Regions Foreign and Commonwealth Office Adapting To Change - UK policy towards the Arctic - ii Foreword “There is no doubt that the Arctic is on the frontier of global climate change impacts. Temperatures are rising twice as fast in the Arctic as over the rest of the world.” The Arctic has proved, time and again, to be As this document sets out, the United Kingdom one of the most dynamic and influential regions will continue to support and respect the sovereign of the world, despite its remoteness from large rights of the Arctic States to exercise jurisdiction population centres and its often challenging over their territory; the people who live and work geographical and climatic conditions. in the Arctic; and the unique and fragile natural environment. At the same time it outlines the The United Kingdom is not an Arctic State, but United Kingdom’s legitimate interests in the we are the Arctic’s nearest neighbour. -
ICE Enforcement and Removal Operations Report
ICE Enforcement and Removal Operations Report Fiscal Year 2014 December 19, 2014 U.S. Immigration and Customs Enforcement . Enforcement and Removal Operations Table of Contents Background ...................................................................................................................... 1 Discussion ........................................................................................................................ 2 Appendix A ...................................................................................................................... 12 Appendix B ...................................................................................................................... 18 i I. Background This report summarizes U.S. Immigration and Customs Enforcement’s (ICE) Fiscal Year (FY) 2014 civil immigration enforcement and removal operations. ICE shares responsibility for enforcing the Nation’s civil immigration laws with U.S. Customs and Border Protection (CBP) and U.S. Citizenship and Immigration Services (USCIS). In executing its enforcement duties, ICE focuses on two core missions: (1) identifying and apprehending public safety threats—including criminal aliens and national security targets—and other removable individuals within the United States; and (2) detaining and removing individuals apprehended by ICE and CBP officers and agents patrolling our Nation’s borders. Each year, ICE immigration enforcement is impacted by operational factors, including the size of the removable population found in the interior and