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Questions and Answers
What is the primary focus of the content provided?
What is the primary focus of the content provided?
Which of the following is NOT a type of drug mentioned?
Which of the following is NOT a type of drug mentioned?
Which is a characteristic feature of narcotic drugs?
Which is a characteristic feature of narcotic drugs?
What best describes the classification of narcotic drugs?
What best describes the classification of narcotic drugs?
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In the context of narcotic drugs, what is an essential precaution?
In the context of narcotic drugs, what is an essential precaution?
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Which of the following statements is FALSE regarding narcotic drugs?
Which of the following statements is FALSE regarding narcotic drugs?
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What is a common misconception about narcotic drugs?
What is a common misconception about narcotic drugs?
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Which substance category is primarily associated with pain relief and can lead to addiction?
Which substance category is primarily associated with pain relief and can lead to addiction?
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What is the primary category associated with the listed substances?
What is the primary category associated with the listed substances?
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Which of the following best describes the regulatory status of narcotic drugs?
Which of the following best describes the regulatory status of narcotic drugs?
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What is a common effect of narcotic drugs on the central nervous system?
What is a common effect of narcotic drugs on the central nervous system?
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Which of the following terms is synonymous with narcotic drugs?
Which of the following terms is synonymous with narcotic drugs?
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Which of these is NOT typically classified as a narcotic drug?
Which of these is NOT typically classified as a narcotic drug?
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Narcotic drugs are mainly derived from which type of source?
Narcotic drugs are mainly derived from which type of source?
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What is one major risk associated with the misuse of narcotic drugs?
What is one major risk associated with the misuse of narcotic drugs?
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What is a common effect associated with narcotic drugs?
What is a common effect associated with narcotic drugs?
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Which of the following is a potential risk associated with narcotic drug use?
Which of the following is a potential risk associated with narcotic drug use?
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Which of the following best describes the term 'narcotic'?
Which of the following best describes the term 'narcotic'?
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Which regulatory body is primarily responsible for the classification of narcotic drugs?
Which regulatory body is primarily responsible for the classification of narcotic drugs?
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Which of the following is not considered a narcotic drug?
Which of the following is not considered a narcotic drug?
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Which of these substances is derived from the opium poppy and classified as a narcotic?
Which of these substances is derived from the opium poppy and classified as a narcotic?
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What type of withdrawal symptoms can occur upon discontinuation of narcotic drugs?
What type of withdrawal symptoms can occur upon discontinuation of narcotic drugs?
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How do narcotic drugs generally affect brain function?
How do narcotic drugs generally affect brain function?
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What is the primary medical use of narcotic drugs?
What is the primary medical use of narcotic drugs?
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What are the main categories of drugs mentioned?
What are the main categories of drugs mentioned?
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Which category of drugs is often associated with inducing sleep?
Which category of drugs is often associated with inducing sleep?
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Which of the following best describes narcotic drugs?
Which of the following best describes narcotic drugs?
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Which of these statements is false regarding narcotic drugs?
Which of these statements is false regarding narcotic drugs?
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What is one of the primary concerns associated with the use of narcotic drugs?
What is one of the primary concerns associated with the use of narcotic drugs?
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Which effects are NOT typically associated with narcotic drugs?
Which effects are NOT typically associated with narcotic drugs?
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What is a common legal use for narcotic drugs?
What is a common legal use for narcotic drugs?
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Which of the following is a potential consequence of the misuse of narcotic drugs?
Which of the following is a potential consequence of the misuse of narcotic drugs?
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Which class of drugs is characterized by their potential for abuse and dependency?
Which class of drugs is characterized by their potential for abuse and dependency?
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What is a significant side effect associated with the use of narcotic drugs?
What is a significant side effect associated with the use of narcotic drugs?
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Which of the following best describes the mechanism of action of narcotic drugs?
Which of the following best describes the mechanism of action of narcotic drugs?
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Which situation might lead to a higher risk of developing tolerance to narcotic drugs?
Which situation might lead to a higher risk of developing tolerance to narcotic drugs?
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What distinguishes narcotic drugs from other classes of analgesics?
What distinguishes narcotic drugs from other classes of analgesics?
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Which of the following is NOT typically considered a narcotic drug?
Which of the following is NOT typically considered a narcotic drug?
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What is a common method of administration for narcotic drugs in a medical setting?
What is a common method of administration for narcotic drugs in a medical setting?
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What class of substances do narcotic drugs belong to?
What class of substances do narcotic drugs belong to?
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Which of the following is a common characteristic of narcotic drugs?
Which of the following is a common characteristic of narcotic drugs?
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Which of the following is NOT typically classified as a narcotic drug?
Which of the following is NOT typically classified as a narcotic drug?
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What is one of the primary uses of narcotic drugs in medicine?
What is one of the primary uses of narcotic drugs in medicine?
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What is a potential risk associated with the use of narcotic drugs?
What is a potential risk associated with the use of narcotic drugs?
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Which of the following statements about narcotic drugs is FALSE?
Which of the following statements about narcotic drugs is FALSE?
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In what form can narcotic drugs be administered?
In what form can narcotic drugs be administered?
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Which factor significantly influences the effectiveness of narcotic drugs?
Which factor significantly influences the effectiveness of narcotic drugs?
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Study Notes
Chemical Analyses of Narcotics in Forensic Laboratories
- This presentation covers chemical analyses of narcotics in forensic labs.
- The presenter (Dr. Mohammed M. El-Gamil) from Mansoura University discusses topics of drug analysis and forensic chemistry.
- The presentation includes a definition of a drug, drug abuse, and historical drug uses.
What is a Drug?
- A substance that induces physiological change upon ingestion.
- Drugs are toxic.
- The dose differentiates a therapeutic drug from a poison.
Definition of a Drug
- A substance that induces a physiological change when ingested.
- Modes of ingestion: swallowing, injection, inhalation, and absorption through the skin.
- Toxicity: All drugs are toxic; the dose differentiates a therapeutic drug from a poison.
- Uses of drugs: treat/prevent disease, alleviate pain, promote sleep, induce physiological responses.
- Paracelsus (1493-1541): "All substances are poisons; the right dose differentiates a poison from a remedy."
Drug Abuse
- Changes over time and varies among societies
- Cocaine in Coca-Cola
- Originally included for stimulation and aphrodisiac effects.
- Invented by John S. Pemberton as "Pemberton's French Wine Cola" in 1885.
- Reformulated to "temperance drink" with coca and kola nut extracts.
- Name derived from kola nut and cocaine.
- Cocaine removed by 1929 due to addiction concerns.
- Historical drug uses
- LSD and MDMA in psychotherapy.
- Methamphetamine used by American soldiers (World War II to Gulf War in 1991).
- Marijuana, medicinally used in ancient times.
- Active ingredient now commercially prepared & marketed as Marinol
Classification of Drugs and Category
- By Origin and Function
- By General Effect
- By Use
- Classification by Schedule
- Their acid-base character
Classification by Origin
- Natural Products
- Extracted from plants.
- Alkaloids: Basic compounds extracted from seed plants.
- Cocaine, THC (tetrahydrocannabinol)
- Semisynthetic Compounds
- Made by modifying natural products.
- Example: Heroin (acetylation of morphine)
- Synthetic Compounds
- Fully synthesized in labs.
- Example: Diazepam (Valium), synthetic THC (dronabinol).
- Challenges in Classification: Ability to synthesize drugs complicates classification by origin.
Classification by General Effect
- Analgesics
- Depressants
- Hallucinogens
- Narcotics
- Stimulants
- Note that drugs may fall into more than one category.
- For example, narcotic drugs are also CNS depressants
Analgesics
- Analgesics relieve pain.
- Examples: aspirin, NSAIDS (as ibuprofen), naproxen sodium, morphine.
- Nonsteroidal anti-inflammatory drugs (NSAIDs)
- Mechanism: Reduce pain by reducing fever and inflammation.
- Action: Block prostaglandins, which are involved in inflammation.
- Result: Prevent synthesis of prostaglandins.
- Morphine and Opiates
- Mechanism: Attach to opioid receptors in CNS and gastrointestinal tract.
- Action: Block nerve impulses relaying pain to the brain.
- Result: Reduce pain by interrupting pain signals.
- Aspirin: Inhibits pain-inducing events and reduces inflammation, non-addictive, does not produce euphoria.
- Morphine: Intercepts pain signals; can cause euphoria and deep relaxation; addictive and classified as a narcotic
Depressants
- Depressants depress central nervous system (CNS) functions.
- Effects: Slowed heartbeat, reduced anxiety, promotion of sleep.
- Examples: Barbiturates, tranquilizers, sleep aids, ethanol.
- Benzodiazepines
- A family of synthetic drugs.
- Common brands: Valium ®.
- Mechanism: Interact with GABA receptors in the brain.
- Action: Bind with GABA receptor sites, generating an inhibitory response.
- Result: Depression of the CNS.
Hallucinogens
- Drugs that alter perception of time, reality, movement, thought, vision, and hearing.
- Examples: LSD, mescaline, marijuana (can act as a hallucinogen at high dose), methamphetamine.
- Pharmacology: Complex, can be generalized into two classes
- Phenethylamines
- Examples: methamphetamine, ecstasy (MDMA).
- Tryptamines
- Example: Psilocybin (from psilocybin mushrooms).
- Phenethylamines
Narcotics
- Effects: Narcotic effects depress the CNS and promote sleep.
- Source: Derived from opium plant (opiate alkaloids).
- Examples: Morphine, codeine, heroin, hydromorphone, oxycodone, hydrocodone.
- Stimulants
- Effects: In contrast to narcotics, stimulants induce alertness, interfere with sleep.
- Common examples: Cocaine, amphetamine, methamphetamine.
- High-dose effects: Many stimulants are hallucinogenic.
- Mechanism: Varies widely. e.g., Cocaine blocks the reuptake of dopamine, leading to generalized stimulation
Classification by Use
- Based on how they are used and their physical/chemical structures and physiological effects within each group.
- Predatory Drugs.
- Commonly used at parties and clubs frequented by young adults as date-rape drugs.
- Purpose: Incapacitate a person for sexual assault (DFSA).
- Common drugs: Ketamine, Rohypnol®, GHB
- Effects: Range from disorientation to unconsciousness; loss of short-term memory.
- Club drugs : Commonly used at parties/clubs by young people.
- Many are also predatory drugs.
- Examples: Ecstasy (MDMA), other hallucinogens (LSD), stimulant-hallucinogens (PCP), methamphetamine
- Human-performance drugs, consist of substances to improve one’s performance
- Examples: Anabolic steroids, alcohol
- Composition: dozens of drugs, mainly prescription-based, derived from testosterone
- Usage: Abused by athletes to increase muscle mass and decrease recovery, commonly found at high school level.
- Inhalants : Inhalants, are substances inhaled to produce desired effects.
- Examples: Paint thinners, nitrous oxide (laughing gas), gasoline, cleaning fluids, nail polish remover.
- Generally depressant effects like alcohol
Classification by Schedule
- The Controlled Substances Act (CSA) regulates drug classifications by the potential for abuse.
- Based on chemical and physiological properties of drugs, and their potential for abuse.
- US - Regulations based on abuse risk.
Drugs as Evidence
- Physical Evidence: The Five P's
- Powders
- Plant matter
- Pills
- Precursors
- Paraphernalia
- Note: All this information pertains to physical evidence of drug use.
Powders
- Range: Colored powders from crystalline white to resinous brown.
- Examples: Heroin, cocaine (plant-derived).
- Characteristics: Many are oily and odoriferous.
Hashish
- Concentrated form of marijuana
- Lies between plant matter and powder.
Plant Matter
- Examples: Marijuana, mushroom, cactus buttons.
- Storage: Must be stored properly to prevent rotting/degradation prior to analysis.
Pills
- Types: Prescription medications, clandestinely synthesized tablets.
- Identification: Visual identification using references like PDR (physician's desk reference).
- Amphetamines, methamphetamine, LSD are often sold in pill form.
- Precursors: Materials used in clandestine drug synthesis
- Methamphetamine precursors: phenyl-2-propanone (P2P), pseudoephedrine.
- LSD precursors: lysergic acd, lysergic amide.
- Drug Paraphernalia: Implements for drug preparation and ingestion.
- Examples: syringes, cookers, pipes, bongs, razor blades, mirrors, straws.
- Challenges: Analysis of trace amounts and identification of chemical residues in the exhibits.
Cutting Agents
- Categories
- Diluents (thinners): Non-drug substances with no pharmacological effects(e.g., baking soda, sugars)
- Adulterants: Active substances with effects like the target drug(e.g., caffeine in cocaine).
- Impurities: Substances found during processing(e.g., codeine in heroin).
- Contaminants: Subcategory of impurities, accidentally introduced during processing (e.g., barium in heroin)
Profiling (Chemical Fingerprinting)
- Analyze drug sample composition beyond identification and quantification.
- Categorize samples into similar groups, determine common origin.
- Elucidate synthetic pathway or extraction method.
- Identify diluents, adulterants, and impurities
- Identify geographic origin for plant-derived exhibits.
- Profiling is increasingly used as an investigative tool.
Profiling a Drug Sample
- Includes physical examination (organic and inorganic analysis).
- Physical Examination: Color, appearance, particle size, microscopic characterization of diluents, and organic analysis.
- Major and minor constituents reveal drug and chemical processing methods.
- Isotopic Ratios: Related to environmental conditions during plant cultivation(stable natural isotopes).
- Informative elements: Nitrogen, calcium, magnesium (from the soil).
Extracted Components
- Plant-derived drugs: Alkaloids extracted from precursor or drug substances.
- Example: Morphine from opium (precursor to heroin).
- Other alkaloids: Codeine, thebaine, papaverine, noscapine.
- Alkaloids interact with morphine during processing.
- Analytical Methods: TLC, GC/MS, HPLC; separate and identify impurities for evidentiary analysis.
Impurities
- Introduced at each processing stage.
- Sources: impure reagents, dirty glassware, contaminated water.
- Solvents: Can carry organic contaminants or be contaminants themselves.
- Residual solvents: Occluded within the crystal matrix of the final salt product.
Adulterants and Diluents
- Provide useful information about batches and groups.
- Common adulterants in heroin: Acetaminophen, caffeine, lidocaine.
- Highly variable and difficult to identify because some are removed during sample preparation.
- Identification can be time-consuming.
- Quick microscopic examination can identify starches or sugars
- Materials like mannitol or baking soda are more challenging to identify.
- Limiting factors in forensic laboratories: caseload and time.
Aspects of profiling a drug sample
- Physical characteristics: appearance, color, and particle size.
- Chemical analysis: Major and minor constituents, adulterants and diluents, impurities, isotopic ratios, and elemental analysis.
Analysis of Seized Drugs
- Focus: Drug analysis and toxicology.
- Presumptive color tests:
- Duquenois-Levine Test (for marijuana)
- Cobalt thiocyanate (for cocaine)
- Marquis Test (for opium derivatives, amphetamines, other alkaloids)
- p-dimethylaminobenzaldehyde (pDMAB) (for LSD)
- Note: These tests give presumptive results, not definitive identification.
Color Tests
- Color tests focus on compounds.
- Functional groups: phenols, aromatic rings, basic nitrogen.
- Many drugs have multiple active molecules.
- Detection limits: presumptive tests generally detect 1 to 50 µg/exhibit.
- Dual Use: Most color test reagents can also be used as developers for thin-layer chromatography (TLC).
- Series of tests performed if sample quantity is sufficient.
Material Indicators
- Green plant material: unlikely to test positive initially for cocaine/heroin.
- Brownish/tarry material: Suggestive of hashish/heroin.
- Blotter papers/gel windows/tiny tablets: Common for LSD.
- Tan or whitish powders/pills: Suitable for extensive color tests. -Note: Some color tests involve precipitation but not all.
Spot Plate / Test Tube
- Spot tests (use glass or ceramic spot plate or disposable test tube)
- Better results on a white background; some tests work better on a black spot plate.
- Place a small amount of the questioned powder in a well on the plate.
- Add the reagent.
- Presumptive tests react with multiple substances.
What is Color?
- Color change indicates chemical reaction; color change points to alteration in chemical bonding during a reaction.
- Colorants: substances absorb or emit electromagnetic energy in the visible range (dyes, pigments).
- Mechanisms of color change in dye formation: changes in molecular structure allowing visible light to interact with molecular orbitals.
- Transition metal complexes: alteration of molecular orbitals allows for visible light interactions; and the reaction between a drug and a reagent creating an energy difference between orbitals enables visible light to promote an electron.
Molecular Orbital Transitions
- Molecular compounds are covalently bonded; atomic orbitals combine to form molecular orbitals.
- White appearance of powder: Reflects all visible light wavelengths; no visible light absorbed.
- White light emitted by broad-spectrum light sources.
- Light appears white when reflected diffusely or at random angles.
- Black appearance: Absorbs all wavelengths.
- Gray appearance: Absorbs a constant percentage of intensity at all wavelengths.
- Achromatic colors: white, gray, and black are colorless.
- Chromatic colors: Specific colors perceived when light is absorbed selectively.
Chromophore and Auxochrome
- Chromophore: The portion of a molecule capable of absorbing a photon; color generation occurs through transitions requiring lower energy photons, smaller transitions energy gaps.
- Conjugation: Decreasing energy gaps allows visible energy to promote electrons.
- Effect of conjugation: leads to absorption of longer wavelengths and a darker perceived color.
- Auxochrome: Not a chromophore itself, it modifies the wavelength/intensity of a chromophore.
- Oxygen and Nitrogen: Contain unshared electrons e and π electrons that interact with aromatic systems.
- Effect on energy gap: Decreases energy gaps and increases the wavelength of absorbed light.
- Removal of unshared pairs of electron; example with anilinium ion shows Amax drops to the value of unsubstituted benzene.
Changes in Wavelength
-
When wavelength increases, the absorbed energy decreases, leading to the color becoming "redder" (red or orange shift).
-
When the wavelength decreases, the absorbed energy increases, leading to the color becoming "bluer" (blue shift).
-
Bathochromic shift: Shift to longer wavelengths (redder light).
-
Hypsochromic shift: Shift to shorter wavelengths (bluer light).
-
Intensity increase: hyperchromic shift: High ελ; highly intense absorption.
-
Intensity decrease: hypochromic shift: lower ελ; less intense absorption.
Dyes and Dye Formation
- Pigment: Insoluble materials in a suspension.
- Dye: Solution of the colorant (solvent).
- Colorants: Can be organic, inorganic, natural, or synthetic.
- Difference in solubility of colorants differentiates a dye from a pigment.
Other Structural Features
- Colored products of presumptive tests frequently contain carbonium ions (carbocations).
- Carbocation: Ion with a positive charge; highly substituted ones tend to be stable.
Marquis Test
- Formaldehyde in sulfuric acid.
- Versatile and widely used color test in drug analysis.
- Complex chemistry, not fully understood.
- Carbocation formation via formaldehyde action; possible free radical mechanism.
- Reaction steps: Formaldehyde adds to aromatic ring with an amine side chain.
- Intermediate product is an alcohol.
- Carbocation is attacked by nucleophiles (alcohol).
- Final product: A dimer with increased conjugation—interaction with visible light.
- Color appearance: Due to increased conjugation.
Marquis Test for Amphetamines
- Marquis reagent reacts with amphetamine and methamphetamine to produce an orange-red product.
- Mechanism involves an attack of the amine of the amphetamine molecule on the carbonyl of formaldehyde.
- The orange color is distinctive.
- Used to differentiate between amphetamine (a primary amine) and methamphetamine (a secondary amine).
The Liebermann Test
- Liebermann reagent (KNO3 dissolved in sulfuric acid) forms nitrous acid (HONO).
- Used to test for phenolic compounds and amines in drug analysis.
- The reaction consists of two steps
- Nitration of the substrate drug, which includes forming a quinon imine derivative
- The coupling is promoted by the sulfuric acid.
- The color produced is pH-dependent.
The Duquenois-Levine Test
- Used for marijuana testing;
- The reaction involves condensation that creates a purple chromophore with the active ingredient tetrahydrocannabinol.
Thin-Layer Chromatography (TLC)
- Rapid analysis technique (rarely longer than 30 minutes), highly sensitive (sub-milligram quantities required), amenable to a wide variety of substances/visualization techniques, and inexpensive.
- TLC plates: Coated with activated silica gel (0.25 mm thickness), optionally with UV-fluorescent additives.
- Available in various sizes depending on sample number and TLC tank size.
- Recommended development length is about 10 cm. Standard sizes include 20x20 cm, 20x10 cm, 10x5 cm used vertically.
- TLC Tanks: Made of clear glass with a tightly fitting lid, lined with adsorbent paper to saturate with solvent vapors.
Spotting
- Spotting Line: Positioned 1 cm from the bottom of the plate.
- Spacing: Minimum 0.8 cm between sample applications; no spot closer than 1.5 cm to the plate's side edge.
- Sample Spot Size: Should be as small as possible (2 mm) to avoid diffuse spots; May require multiple small aliquots to achieve a small diameter spot.
- Drying Spots: Can use cold or hot air between applications; ensure no thermally labile components if using hot air.
Developing Solvent
- Prepare developing solvents accurately using pipettes and measuring cylinders.
- Automatic dispensers can be used.
- Mix solvents can be done within the TLC tank for saturation with solvent vapors.
- Sufficient time for saturation (approximately 5 minutes using paper-lined tanks).
- For development systems, renew solvent after 3 runs or ideally after each development.
Development Line Position
- For a 20 cm TLC plate, scratch 11 cm from bottom (spotting end).
- For a 10 cm TLC plate, end of the plate is the development line.
- Stop analysis when solvent reaches the development line.
- During monitoring, analysts must monitor solvent progress on the TLC
- Remove the plate from the tank as soon as the solvent reaches the development line to avoid diffuse spots.
Standard Solutions
- Prepare concentrations of heroin, morphine, codeine, acetylcodeine, 6-acetylmorphine, papaverine, and noscapine at 1 mg/ml in methanol.
Sample Preparation
- Suitable materials for isolating heroin, opium, and crude morphine from seized materials.
- Dissolve 5 mg of sample per 1 ml of methanol.
- Place 1 µl or 5 µl spots onto the TLC plate.
Drying Plates
- Must be dry before visualization.
- Dry at room temperature, in an oven (120°C maximum), or a hot air blower.
- Ensure that all traces of ammonia are removed for proper color development before analysis.
Visualization Methods
- UV Light (254 nm, if silica gel contains a fluorescent additive).
- Dragendorff's spray reagent; produces orange spots on a yellow background with opium alkaloids.
- Acidified potassium iodoplatinate spray reagent; produces bluish-to-purple spots with opium alkaloids.
Rf values
- Small changes in TLC plate composition and solvent systems can result in significant changes in Rf values for individual compounds.
- Analysts should only compare data with reference standards applied to the same TLC plate as the sample to maintain consistency.
Gas Chromatography (GC)
- Packed column methods (Method A)
- Capillary column methods (Megabore capillary column, Narrow Bore capillary column, Method B)
- Column Efficiency and Resolving Power (expressed in theoretical plates/meter):
- Packed column: ~200 plates/m.
- Megabore capillary column: ~1,500 plates/m
- Narrow bore capillary column: ~4,000 plates/m
GC-Packed Column Method (Method A)
- Detector: FID.
- Column: 6 ft (or 2 m) x 2-4 mm I.D.
- Packing: 3% Dimethyl silicone (SE-30 or OV-2)
- Carrier gas: N2 at 70 ml/min
- Injection size: 2-5 µL as appropriate
- Temperatures (oven, injector, detector): 275 °C, 275 °C, 230 °C, respectively.
- Internal standard: n-Docosane (100 mg/5.0 ml methanol).
- Derivatization reagent: N,O-bis(trimethylsilyl)acetamide (BSA)
Preparation of Samples and Standard Solutions (GC)
- Derivatization
- To 0.5 ml of standard solution, add 0.5 ml of BSA in a stoppered vial, heat at 100°C for 10 minutes.
- Treat 0.5 ml of the heroin sample solution in the same manner.
Elution order (GC)
- Order of elution varies with specific GC conditions
Conditioning of Packed Columns
- Condition all packed columns before use at a temperature at least 30°C above the maximum operating temperature.
- Typically condition columns overnight for a minimum of 15 hours.
- Ensure a leak-free injection system.
- Maintain normal gas flow.
- Disconnect column from detector during conditioning.
- Frequently saline glass columns to prevent morphine adsorption during GC determinations, and maintain a leak-free system.
GC-MS Methodology and Operating Conditions
- GC/MS Method (Method B)
- Column: Fused silica (30 m x 0.25 mm I.D.) with 0.25 µm chemically bonded dimethylpolysiloxane stationary phase.
- Carrier Gas: Helium (He) at 50 cm/sec at 220 °C oven temperature.
- Injection technique: Split (1:15 ratio); injection volume 1 µL.
- Temperatures: Injector = 250 °C, MS source = 275 °C, Oven = 310 °C (with a 150°C hold time and 9 °C/minute temperature change up to 300°C and a 2.4-minute hold time, or 5.4 if for opium/morphine).
- Internal standard: n-tetracosane.
- Derivatization reagent: N-Methyl-N-trimethylsilyltrifluoroacetamide (MSTFA).
Elution order (GC-MS)
High-Performance Liquid Chromatography (HPLC)
- Method A
- Detector: UV at 280 nm
- Column: Octadecyl-silica, 300 x 3.9 mm I.D. (µBondapak C18 or equivalent)
- Mobile Phase: Water, acetonitrile, triethylamine
- Flow rate: 2ml/min
- Injection volume: 5-20 μl
- Standard: 10 ml of mobile phase with 10mg of Morphine (base or hydrochloride) accurately weighed and dissolved
- Note: Procedure will vary depending on the specified method.
Sample preparation (HPLC)
- Opium sample preparation:
- Disperse 100 mg of opium with 10 ml of saturated aqueous sodium chloride (adjust pH with dilute ammonia).
- Extract the mixture three 20-ml portions of chloroform/isopropanol (3:1).
- Filter the organic layers througn anhydrous sodium sulfate or phases separation paper and evaporate the organic solvent to dryness.
- Take the residue up in 10 ml of mobile phase.
- Morphine sample preparation: Same method as Morphine standard solution; accurately weigh 10mg of Morphine sample and dissolve in 10ml of mobile phase.
Elution Order (HPLC)
- Morphine → Codeine → Thebaine → Noscapine → Papaverine
Calculation Notes
- Standard solutions
- Close proximity (same order of magnitude).
- Multi-point validation
- Include negative standard (blank) samples to ensure no phantom responses for target compounds or internal standards.
- Include one or more blank(s) before and after the analytical run for less than 15 samples, and at least one additional blank midway through for >15 samples.
General Quantitation Notes
- Calibration curves must be constructed for each compound.
- Use at least three points with concentrations above and below expected quantity of compound.
- Verification is needed for any curve change to ensure method validity.
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Test your knowledge on narcotic drugs with this comprehensive quiz. Explore the classification, characteristics, misconceptions, and regulatory status of narcotic substances. Be prepared to identify their effects and associated risks.