Controlled Substances Technical Manual, 06-01-2018
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Welcome to the 2021 IDS Forensic Science Education Series • Do today: Attorneys – if you would like CLE credit, report your attendance to me using the link that I email you and I will submit your information to the bar. The State Bar will invoice you for $3.50 per hour of CLE credit at the end of the credit year. 60 min of general CLE credit is anticipated. You may only receive credit for attending the live (not recorded) version of the webinar. • Do later: For participants who complete 10 or more webinars in this year’s series and report their credit to me, you’ll receive acknowledgement that you completed this course of forensic education. For this certificate, watching the recorded version is fine. Please report this attendance to me in Dec. 2021. • I will email you the link to report your attendance to me. • Questions? Email [email protected] Edward G. Brown, Ph.D. NC Indigent Defense Services CLE April 1, 2021 Edward G. Brown, Ph.D. Dr. Brown obtained his Bachelor of Science degree in Chemistry from U.C. Berkeley in 1980 and his Doctoral degree in Organic Chemistry from U.C. Davis in 1988. Two post- doctoral chemistry research fellowships from University of Auckland, New Zealand, and Yale University furthered his academic studies in medicinal chemistry and analytical chemistry techniques through 1990. Dr. Brown’s productivity during his career as a medicinal and organic chemistry researcher in academics and while working at several pharmaceutical companies and other laboratories has led to his co-inventorship on ten US patents and his co- authorship on over thirty research articles and conference presentations. -
Screening/Spot Test of Narcotics
Indian Journal of Forensic and Community Medicine 2020;7(4):160–165 Content available at: https://www.ipinnovative.com/open-access-journals Indian Journal of Forensic and Community Medicine Journal homepage: https://www.ipinnovative.com/journals/IJFCM Review Article Screening/spot test of narcotics A K Jaiswal1,*, Kamna Sharma2, Rohit Kanojia3, Sally Lukose4 1Dept. of Forensic Medicine & Toxicology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India 2Galgotias University, Greater Noida, Uttar Pradesh, India 3Dept. of Chemistry, University of Delhi, New Delhi, India 4CTM-IRTE, Faridabad, Haryana, India ARTICLEINFO ABSTRACT Article history: Narcotics are the substances used to treat moderate to severe pain. They could be natural like opiates such Received 25-11-2020 as morphine, codeine etc., synthetic like fentanyl, methadone etc., and semi-synthetic like oxycodone, Accepted 02-12-2020 hydrocodone etc. These drugs act as pain relievers, induces the state of stupor or sleep, and increase Available online 08-01-2021 the physical dependence on them. In forensic autopsy case, the forensic pathologist may require a complete toxicological investigation for different poisons including stimulants. In India, Forensic Science Laboratories run by Government under the Home ministry usually carry out this. The samples must be Keywords: analysed by the forensic toxicologist/chemists/scientist. This article deals with the screening/spot test for Narcotics narcotics. It attempts to simplify the standard procedures in a step-wise manner, which can be of handy Screening reference for the forensic toxicologist. Spot test Drugs © This is an open access article distributed under the terms of the Creative Commons Attribution Opioids etc License (https://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. -
Seized Drugs Technical Manual, 12-08-2020
Seized Drugs Technical Manual Approval Date: 12/08/2020 Document Number: 4561 Approved By: David Gouldthorpe, Kim Murga, Cassandra Robertson Revision Number: 17 Date Published: 12/08/2020 Las Vegas Metropolitan Police Department Forensic Laboratory 5605 W. Badura Ave. Ste. 120B Las Vegas, NV 89118 Seized Drugs Technical Manual Uncontrolled Copy if not located in Qualtrax Page 1 of 166 Seized Drugs Technical Manual Approval Date: 12/08/2020 Document Number: 4561 Approved By: David Gouldthorpe, Kim Murga, Cassandra Robertson Revision Number: 17 Date Published: 12/08/2020 Table of Contents Chapter Title Introduction ANALYTICAL TECHNIQUES 1.1 Color Tests 1.2 Chromatography 1.3 Mass Spectrometry (MS) 1.4 Infrared Spectroscopy (IR) 1.5 X-Ray Fluorescence (XRF) 1.6 Raman Spectroscopy QUALITY CONTROL 2.1 Reference Materials and Supplies 2.2 Reference Material Inventory Audit 2.3 Color Test Reagent Quality Control 2.4 Quality Control Plan SEIZED DRUG ANALYSIS 3.1 Seized Drugs Analysis Quality Control 3.2 Sampling 3.3 Identification Criteria 3.4 Evidence Discrepancies and Preliminary Field Test Errors 3.5 Cannabis Analysis 3.6 Opium Analysis 3.7 Analysis of Fentanyl and Fentanyl Related Substances CLANDESTINE LABORATORIES 4.1 Clandestine Laboratory Response 4.2 Clandestine Laboratory Analysis REPORTING AND TECHNICAL REVIEW 5.1 Reporting 5.2 Technical Review 6 Retraining 7 Recipes and Derivatizing Agents PROCEDURES 8.1 Logging Reference Materials into LIMS 8.2 Verifying Reference Materials Uncontrolled Copy if not located in Qualtrax Page 2 of 166 -
Drug Chemistry Procedure Manual 1
Drug Chemistry Procedure Manual 1 SECTION A: Preliminary Tests Marquis Reagent ..................................................................................................... A - 1 Duquenois-Levine Reagent .................................................................................... A - 2 Cobalt Thiocyanate Reagent .................................................................................. A - 3 Ferric Chloride Reagent ......................................................................................... A - 4 Koppanyi Reagent................................................................................................... A - 5 Potassium Permanganate Reagent ...................................................................... A - 6 p-Dimethylaminobenzaldehyde Reagent (PDMAB) .............................................. A - 7 Froehde’s Reagent.................................................................................................. A - 8 Mecke’s Reagent..................................................................................................... A - 9 Silver Nitrate Reagent............................................................................................. A - 10 Zwikker Reagent...................................................................................................... A - 11 Barium Chloride Reagent ....................................................................................... A - 12 Methanolic Potassium Hydroxide Reagent ......................................................... -
Chemistry Exam - 2015
Scientific Officer Chemistry Exam - 2015 (Final Answer Key) Chemistry Q.No: 1 The major detoxification reaction involved in Phase - I are all except. A Oxidation B Hydrolysis C Acetylation D Hydroxylation Q.No: 2 Which of the endogenous substance is detoxified through glucuronidation reaction ? A Aspirin B Methanol C Bilirubin D Phenyl Acetate Q.No: 3 Which of the following is not a conjugating agent in drug metabolisim? A Active acetate B Active sulfate C Active glucuronate D Active Bicarbonate Q.No: 4 Which of the following statements is not true about receptors ? A Most receptors are proteins situated in the cell membrane B Receptors contain a cleft- known as binding site C Receptors catalyze reactions on chemical messengers D Receptors bind to chemical messengers e.g. neurotransmitters etc Q.No: 5 The mechanism behind pesticide poisoning is A Irreversible binding with Acetyl choline esterase B Reversible binding with Acetyl choline esterase C Irreversible binding with nicotinic receptors D Reversible binding with nicotinic receptors Q.No: 6 Which one of the following have binding affinity but no intrinsic activity? A Agonist B Antagonist C Partial Agonist D Inverse Agonist Q.No: 7 Which of the following is not a requirement for a drug to act as an agonist ? A Functional group B Metabolic stability C Pharmacophore D Size Q.No: 8 Polycyclic aromatic hydrocarbons (PAH) in cigarette smoke may cause - A Inhibition of cytochrome P-450 and delayed metabolism B Inhibition of cytochrome P-450 and enhanced metabolism C Induction of cytochrome -
INTERNATIONAL COLLABORATIVE EXERCISES (ICE) Summary Report
INTERNATIONAL QUALITY ASSURANCE PROGRAMME (IQAP) INTERNATIONAL COLLABORATIVE EXERCISES (ICE) Summary Report SEIZED MATERIALS 2015/1 INTERNATIONAL QUALITY ASSURANCE PROGRAMME (IQAP) INTERNATIONAL COLLABORATIVE EXERCISES (ICE) Table of contents Introduction Page 3 Comments from the International Panel of Forensic Experts Page 3 NPS reported by ICE participants Page 4 Codes and Abbreviations Page 7 Sample 1 Analysis Page 8 Identified substances Page 8 Statement of findings Page 12 Identification methods Page 21 Summary Page 26 Z-Scores Page 27 Sample 2 Analysis Page 31 Identified substances Page 31 Statement of findings Page 35 Identification methods Page 44 Summary Page 49 Z-Scores Page 50 Sample 3 Analysis Page 53 Identified substances Page 53 Statement of findings Page 55 Identification methods Page 60 Summary Page 65 Sample 4 Analysis Page 66 Identified substances Page 66 Statement of findings Page 71 Identification methods Page 80 Summary Page 85 Z-Scores Page 86 Full test Samples Information Samples Comments on samples Sample 1 SM-1 was prepared from a seizure containing 5.2 % (w/w) cocaine base. The test sample also contained glucose, caffeine, lidocaine, procaine and trace amounts of creatine and levamisole. Sample 2 SM-2 was prepared from a seizure containing 5.5 % (w/w) amfetamine base. The test sample also contained caffeine and creatine. Sample 3 SM-3 was a blank test sample containing no substances from the ICE menu. Sample 4 SM-4 was prepared from a seizure containing 72.2%(w/w) heroin base. the seizure also contained acetylcodeine, -
By HENRYDEANE, F.L.S., and HENRYB
View Article Online / Journal Homepage / Table of Contents for this issue 34 DEASE AND BRADY ON MICROSCOPICAL VIIP.-On ikIicroscopicu2 Research in relation to Pharmacy. By HENRYDEANE, F.L.S., and HENRYB. BRADY,F.L.S. [Read at the Bath Meeting of the British Pharmaceutical Conference, Sept., 1864.1 WE have chosen for the particular subject of the present commu- nication the various preparations of opium. Whether regarded in respect to their importance in the practice of medicine, their variability in strength and character, or the peculiar conditions in which the active matter exists in the crude drug, no better subject could be found for the purpose in view. Opium, as is well known, is an extremely composite substance, being a pasty mass formed of resinous, gummy, extractive and albuminous matters, containing a larger or srrialler percentage of certain active principles diffused through it. These principles are morphine, narcotine (with its two homologuesj, codeine, narceine, mecoiiine, thellaine, and papaverine, either existing free or in com- bination with meconic, sulphuric, or other acids, the sum of the crystalline constituents, exclusive of inorganic salts, contained in good samples of the drug, being from twenty to thirty per cent. of its entire weight. Any preparation, exactly to represent opium, must contain the whole of' these principles, as indeed the tincture may be said fairly to do. It, has, however, been shown that some of the principles are inert, and others even deleterious in their action, and we have Published on 01 January 1865. Downloaded by University of Pittsburgh 30/10/2014 05:40:05. -
For Peer Review 19 Studies
Drug Testing and Analysis A review of chemical ‘spot’ tests: a presumptive illicit drug identification technique Journal:For Drug Peer Testing and Analysis Review Manuscript ID DTA-17-0289.R1 Wiley - Manuscript type: Review Date Submitted by the Author: n/a Complete List of Authors: Philp, Morgan; University of Technology Sydney, Centre for Forensic Science Fu, Shanlin; University of Technology Sydney, Centre for Forensic Science presumptive identification, color test, new psychoactive substances, Keywords: chemistry Chemical ‘spot’ tests are a presumptive illicit drug identification technique commonly used by law enforcement, border security personnel, and forensic laboratories. The simplicity, low cost and rapid results afforded by these tests make them particularly attractive for presumptive identification globally. In this paper, we review the development of these long- established methods and discuss color test recommendations and guidelines. A search of the scientific literature revealed the chemical Abstract: reactions occurring in many color tests are either not actively investigated or reported as unknown. Today, color tests face many challenges, from the appearance of new psychoactive substances to concerns regarding selectivity, sensitivity, and safety. Advances in technology have seen color test reagents used in digital image color analysis, solid sensors and microfluidic devices for illicit drug detection. This review aims to summarize current research and suggest the future of presumptive color testing. http://mc.manuscriptcentral.com/dta Page 1 of 34 Drug Testing and Analysis 1 2 3 A review of chemical ‘spot’ tests: a presumptive illicit drug identification 4 5 technique 6 7 Morgan Philp and Shanlin Fu 8 9 10 11 Short title: Review of chemical spot tests for illicit drug detection 12 13 Chemical ‘spot’ tests are a presumptive illicit drug identification technique commonly used 14 by law enforcement, border security personnel, and forensic laboratories. -
Dr. Duke's Phytochemical and Ethnobotanical Databases Chemicals Found in Papaver Somniferum
Dr. Duke's Phytochemical and Ethnobotanical Databases Chemicals found in Papaver somniferum Activities Count Chemical Plant Part Low PPM High PPM StdDev Refernce Citation 0 (+)-LAUDANIDINE Fruit -- 0 (+)-RETICULINE Fruit -- 0 (+)-RETICULINE Latex Exudate -- 0 (-)-ALPHA-NARCOTINE Inflorescence -- 0 (-)-NARCOTOLINE Inflorescence -- 0 (-)-SCOULERINE Latex Exudate -- 0 (-)-SCOULERINE Plant -- 0 10-HYDROXYCODEINE Latex Exudate -- 0 10-NONACOSANOL Latex Exudate Chemical Constituents of Oriental Herbs (3 diff. books) 0 13-OXOCRYPTOPINE Plant -- 0 16-HYDROXYTHEBAINE Plant -- 0 20-HYDROXY- Fruit 36.0 -- TRICOSANYLCYCLOHEXA NE 0 4-HYDROXY-BENZOIC- Pericarp -- ACID 0 4-METHYL-NONACOSANE Fruit 3.2 -- 0 5'-O- Plant -- DEMETHYLNARCOTINE 0 5-HYDROXY-3,7- Latex Exudate -- DIMETHOXYPHENANTHRE NE 0 6- Plant -- ACTEONLYDIHYDROSANG UINARINE 0 6-METHYL-CODEINE Plant Father Nature's Farmacy: The aggregate of all these three-letter citations. 0 6-METHYL-CODEINE Fruit -- 0 ACONITASE Latex Exudate -- 32 AESCULETIN Pericarp -- 3 ALANINE Seed 11780.0 12637.0 0.5273634907250652 -- Activities Count Chemical Plant Part Low PPM High PPM StdDev Refernce Citation 0 ALKALOIDS Latex Exudate 50000.0 250000.0 ANON. 1948-1976. The Wealth of India raw materials. Publications and Information Directorate, CSIR, New Delhi. 11 volumes. 5 ALLOCRYPTOPINE Plant Father Nature's Farmacy: The aggregate of all these three-letter citations. 15 ALPHA-LINOLENIC-ACID Seed 1400.0 5564.0 -0.22115561650586155 -- 2 ALPHA-NARCOTINE Plant Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. 17 APOMORPHINE Plant Father Nature's Farmacy: The aggregate of all these three-letter citations. 0 APOREINE Fruit -- 0 ARABINOSE Fruit ANON. -
Seized Drugs Technical Manual
Seized Drugs Technical Manual Approval Date: 06/12/2019 Document Number: 4561 Approved By: David Gouldthorpe, David Johnson, Cassandra Robertson Revision Number: 12 Date Published: 06/12/2019 Las Vegas Metropolitan Police Department Forensic Laboratory 5605 W. Badura Ave. Ste. 120B Las Vegas, NV 89118 Seized Drugs Technical Manual ARCHIVED Uncontrolled Copy if not located in Qualtrax Page 1 of 167 Seized Drugs Technical Manual Approval Date: 06/12/2019 Document Number: 4561 Approved By: David Gouldthorpe, David Johnson, Cassandra Robertson Revision Number: 12 Date Published: 06/12/2019 Table of Contents Chapter Title Introduction ANALYTICAL TECHNIQUES 1.1 Color Tests 1.2 Chromatography 1.3 Mass Spectrometry (MS) 1.4 Infrared Spectroscopy (IR) 1.5 X-Ray Fluorescence (XRF) 1.6 Raman Spectroscopy QUALITY CONTROL 2.1 Reference Materials and Supplies 2.2 Reference Material Inventory Audit 2.3 Color Test Reagent Quality Control 2.4 Quality Control Plan SEIZED DRUG ANALYSIS 3.1 Seized Drugs Analysis Quality Control 3.2 Sampling 3.3 Identification Criteria 3.4 Evidence Discrepancies and Preliminary Field Test Errors 3.5 Marijuana Analysis 3.6 Opium Analysis 3.7 Analysis of Fentanyl and Fentanyl Related Substances CLANDESTINE LABORATORIES 4.1 Clandestine Laboratory Response 4.2 ARCHIVEDClandestine Laboratory Analysis REPORTING AND TECHNICAL REVIEW 5.1 Reporting 5.2 Technical Review 6 Retraining 7 Recipes and Derivatizing Agents PROCEDURES 8.1 Logging Reference Materials into LIMS Uncontrolled Copy if not located in Qualtrax Page 2 of 167 Seized -
Crude Drugs Containing Quinoline, Isoquinoline, And
CRUDE DRUGS CONTAINING QUINOLINE, ISOQUINOLINE, AND PHENANTHRENE ALKALOIDS Content 1. MACROMORPHOLOGICAL EVAULATION Cinchonae cortex Ipecacuanhae radix Chelidonii herba Papaveris maturi fructus Opium crudum Fumariae herba 2. MICROSCOPICAL TESTS Cross section: Cinchonae cortex Ipecacuanhae radix Powder preparation: Cinchonae cortex 3. PHYSICO-CHEMICAL AND CHEMICAL TESTS Specific alkaloid reactions 3.1. Grahe test (Cinchonae cortex) 3.2. Emetine test (Ipecacuanhae radix) 3.3. Marquis test (Papaveris maturi fructus) 3.4. Meconic acid test (Papaveris maturi fructus) 3.5. Chelidonii herba tests (Chelidonii herba) 3.5.1. Chelidonic acid test (Chelidonii herba) 3.5.2. Quaternary amine test (Chelidonii herba) 3.5.3. Chromotropic acid test (Chelidonii herba) 3.5.4. Chelidonii herba alkaloid investigation with TLC 4. QUANTITATIVE DETERMNATIONS 4.1. Determination of alkaloid content in Cinchonae cortex (Ph.Eur.) 4.2 Quantitative determination of morphine in ripped capsules of poppy by TLC 1 1. MACROMORPHOLOGICAL EVALUATION Cinchonae cortex Cinchona bark Cinchona pubescens Vahl. Rubiaceae (Cinchona succirubra Pavon) C. calisaya (Weddell) C. ledgeriana (Moens ex Trimen) Ph. Eur. Whole or cut, dried bark of Cinchona species. Content: minimum 6.5 per cent of total alkaloids, of which 30 %- 60 % consists of quinine type alkaloids (dried drug). Ipecacuanhae radix Ipecacuanha root Cephaelis ipecacuanha (Brot.) A.Rich. Rubiaceae Cephaelis acuminata Karsten Ph. Eur. Karlten Ipecacuanha root consists of the fragmented and dried underground organs of Cephaelis species. It contains not less than 2.0 per cent of total alkaloids, calculated as emetine. The principal alkaloids are emetine and cephaeline. Chelidonii herba Greater Celandine Chelidonium majus L. Papaveraceae Ph.Eur. Dried, whole or cut aerial parts of Chelidonium majus L collected during flowering. -
OPIUM Latest Revision: June 30, 2000
OPIUM Latest Revision: June 30, 2000 1. SYNONYMS CFR: Opium CAS #: Codeine Base: 76-57-3 Codeine Hydrochloride: 1422-07-7 Morphine Base: 57-27-2 Morphine Hydrochloride: 52-26-6 Thebaine Base: 115-37-7 Noscapine Base: 128-62-1 Noscapine Hydrochloride: 912-60-7 Papaverine Base: 58-74-2 Papaverine Hydrochloride: 61-25-6 Other Names: Oil poppy Opium poppy 2. CHEMICAL AND PHYSICAL DATA The immediate precursor of heroin is morphine, and morphine is obtained from opium. Opium is the dried milky juice (latex) obtained from the unripe seed pods of Papaver somniferum L., more commonly referred to as the opium poppy or oil poppy. Morphine has also been reported to be present in Papaver setigerum, and as a minor alkaloid in Papaver decaisnei and Papaver rhoeas. However, there is no known instance of these poppies being used for opium production, and work that is more recent has cast considerable doubt as to the presence of morphine in Papaver rhoeas. A major review by Kapoor on the botany and chemistry of the opium poppy is recommended additional reading. Opium latex is obtained from the seed capsule of the poppy while the capsule is still in the green stage, usually seven or more days after flowering and petal fall. Physically, the opium latex is contained within laticiferous vessels, which lie just beneath the epicarp of the seed capsule. The latex is harvested by making a series of shallow incisions through the epicarp, which allows the latex to "bleed" onto the surface of the seed capsule. Most commonly, the latex is allowed to partially dry on the capsule surface, and is then removed by scraping the capsule with specially designed hand tools.