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 Toxicology: Classification of drugs;

- Study of poisonous substances, their actions on the living - According to origin


organisms, their detection by laboratory methods and measures o Natural or Synthetic
taken to counteract their biologic effects - According to legal classification (Philippines)
- Study of substances introduced into the body o RA 9165: Comprehensive Dangerous Drug Act of 2002
- Toxicos = poison; Logos = study o PD 1619: for volatile substances (rugby, thinners)
- All drugs of abuse (except barbiturates and cannabinoids) are: o RA 6425: Dangerous drugs act of 1972; prohibited and
o Basic amino group - containing compounds regulated drugs
o Mostly contain benzene rings - According to international classification
o Narcotics: Produces sleep, stupor and relieves pain
Therapeutic drug monitoring o Psychotropic substances: Any drug having a particular
- Branch of clinical chemistry that specializes in measurement of affinity or effect on the psyche
medication levels in the blood o Designer drugs: Related to but slightly different from
- Main focus = drugs by narrow therapeutic ranges (drugs that can controlled substances, designed by clandestine chemist
usually be over or underdosed) - According to effects
o Stimulants: Increase alertness and physical disposition
Indications: (Amphetamines, caffeine, cocaine, methamphetamine,
- To determine the relationship between plasma drug shabu)
concentration and pharmacologic effects o Hallucinogens: Drugs that affect sensation, thinking, self-
- Knowledge of the drug level influences management awareness, emotion (Ecstasy, Lysergic acid diethylamide
- Narrow therapeutic window (LSD), Marijuana, mescaline, phencyclidine (PCP),
- Potential patient compliance problems psilocybin)
- Drug doses can't be optimized by clinical observation alone o Narcotics: Drugs that relieve and induce sleep (Codeine,
heroin, morphine)
Reasons: o Sedatives/Depressants: Drugs that reduce anxiety and
- Non-therapeutic: Dose too low, malabsorption, rapid metabolism excitement (Alcohol, barbiturates)
- Toxic levels: Overdose (dose too high or too frequent), reduced
renal function, reduced hepatic metabolism Drug techniques in serum and urine:

Drug action 1. Immunochemical method


1. Replacing / acting substances for missing chemicals a) Enzyme mediated for immunologic techniques (EMIT)
2. Increase or stimulate certain activities b) Fluorescent polarization
3. Decrease or slows down certain activities - Principle: competitive binding immunoassay
4. Interferes with the functions of foreign cells o Direct competition: Immobilized drug conjugate competes
with drug/metabolites of a limited amount of chemical
Factors influencing the relationships between drug dosage and the labeled antibody
intensity of its effect: o Displacement: Displacement of a chemically labeled drug
1. Drug prescribed — compliance; correct drug conjugate already bound to an equal amount of test
2. Dose taken — absorption, distribution, metabolism, excretion antibody.
3. Plasma concentration — diffusion or active transport protein
binding in blood 2. Chromatographic procedures
4. Concentration at the site of action — tissue responsiveness; a) Thin layer chromatography (TLC)
effects of other drugs b) High performance liquid chromatography (HPLC)
5. Intensity of effects—over or underdose - Cross reactivity (interferences):
o Drug and drug metabolites with significant structural
Factors of body response to drugs: similarities to the target analyte may cross-react with target
1. Weight, age, gender analyte specific antibodies, producing false positive results
2. Physiological factors: diurnal rhythm of nervous and endocrine o Degree to which any substrate other than the target
system, acid-base balance, hydration and electrolyte imbalance. substrate interacts with an antibody
3. Others: Pathologic factors, Immunological factors, Environmental
factors, Tolerance, Accumulation Drug metabolism:
- Drug administration: oral, intravenous, inhalation
Areas of toxicology - Drug detection: depends on the ff:
1. Detection of drug of abuse 1. Absorption: structure and composition, diffusion and
2. Monitoring therapeutic drug level transport, physiochemical factors in penetration
3. Detection of environmental consciousness 2. Disposition: distribution, pH partition principle,
4. Detection of toxin in poisons electrochemical and donnan distribution, biotransformation
3. Elimination
Drug
- A chemical substance that brings about physical, physiological, Biotransformation:
behavioral and/or psychological change in a person taking it. - Degradative: Drug molecule is diminished to a smaller structure
- A chemical substance other food which is intended to affect the - Synthetic: 1 or more atoms may be added to the molecule
structure or function of the body of man or animal - Phase I: oxidation, reduction and hydrolysis
- All medicine are drugs but not all drugs are medicine - Phase II: conjugation (esterification, amidation, mixed anhydride
formation, hemiacetal formation, etherization).
Drug abuse
- Any non-medical use of drugs that cause physical, psychological, Drugs of abuse: Cocaine, Opium, Tranquilizer, Sedatives, Dopaminergic
legal, economic, or social damage to the user or to people pathway stimulants, Hallucinogens
affected by the user's behavior
- Abuse usually refers to illegal drugs but may also be applicable to In the Philippines: What are the drugs tested?
drugs that are available legally, such as prescribed medications 1. Most common: marijuana, cocaine, amphetamine, opiates, PCP
and certain over-the-counter medications 2. Other popular tests: methamphetamines, benzodiazepines,
barbiturates, oxycodone, ecstasy.
Neurons: functional subunits of the nervous system; have nerve fibers Opioids
- 2 types of nerve fibers: - Provides a quick, intense feeling of pleasure followed by a sense
1. Axons - impulse is sent away from the cell body of well-being and calm
2. Dendrites - impulse is delivered to the cell body - Screening tests: Immunoassay method
- Confirmatory test: GC-MS
Major tranquilizers: - Types of Opiates:
- Example is Haloperidol (Haldol) 1. Naturally-occurring: from Papaver samniferum (opium
- Used to treat psychotic states such as schizophrenia poppy) = Opium, Morphine, and Codeine
- Block attachment of dopamine to dendritic receptors in the 2. Semi-synthetic = Heroin, Hydromorphone, and Oxycodone
synapse blocking stimulatory effects of dopamine 3. Synthetic = Moperidine (Demerol), Fentanyl (Sublimaze),
Propoxyphene (Darvon), Methadone (Dolophine)
Specimens that can be used in toxicology: - Treatment: Naloxone (Narcan): a specific opiod antagonist that
- Urine, Blood, Hair (used for Arsenic poisoning), Meconium (1st reverses CNS depression
bowel movement of the fetus; nicotine and cocaine), Saliva,
Sweat (for detecting tetrahydrocannabinol, amphetamine, PCP) Opium
- Street name: Blanco, Brown sugar, Kabayo, Kengkoy, Gamot,
Drugs of abuse Matsakao, Pulbos, Sapsap, Tinik
1. Depressants / Downers— tranquilizers, sedative - Uses: relief of intense pain, cough suppression, treatment of
2. Stimulation— cocaine, amphetamine diarrhea, anesthesia
3. Hallucinogens— LSD, PCP - Symptoms of abuse: shallow respiration, pinpoint pupils,
4. Analgesics and antidepressants—acetaminophen, salicylates, hypothermia
tricyclic antidepressants - Route of administration: Intravenous
- Half life: 3 minutes (IV route); effect lasts for 3 hours
Cocaine
- Street name: Coke, Crack, Gold dust, Star dust, White girls, Speed Morphine
balls - Street name: M, Dreamer, Ms. Emma, Cube juice, hard stuff,
- From coca plant; used also in coca-cola Morph, emsel, pulbos
- Derivative of the alkaloid ecgonine - Can relieve pain and induce sleep
- Has dopaminergic effects induces increased calcium influx in - Derivative of opium, metabolite of heroin
dopaminergic neurons: - Uses: Powerful analgesic, Treatment of acute congestive heart
o This activates the phospholipases as second messengers failure
o Release of dopamine in the synapse - Toxicity manifestations: Coma, Pinpoint pupils, Depressed
- Cytotoxic effect: formation of nitric oxide free radical produced in respiration
the metabolism in the liver
- Limbic system: cAMP for dopamine release Codeine
- Half-life: 1 – 2 hours - Street name: School boy
- Usually cleared within 2 days - Major metabolites: N-acetyl morphine and Morphine
- Used as: Additive in certain foods, Local anesthesia (usually during - Used as: a mild analgesic and as an anti-tussive
nasopharyngeal surgery) - Route of administration: Intravenous
- Route of administration: Nasal (snorting) - Highly addictive = Addiction recognized by: needle tracks
- Potent form: Crack cocaine (free base or purest form) - Analog: dextromethorphan (D-3-Methoxy-N-Methylmorphine)
o Passes rapidly across nasal membrane where most or all of it o Generally not addictive
enters the bloodstream rapidly o Recommended dose: 15 — 30 mg; 3-4 times a day
- Fatalities have 2 types: o Light intoxication = 100 — 200 mg
1. Direct toxicity of the drug o Heavy intoxication = around 1500 mg
2. Crime related to the illicit acquisition o Block NMDA receptors (like PCP):
- Large doses cause: Euphoric state ("high"), Hallucination, Violent 1. Neuronal plasticity and memory
behavior, Delusion (strong belief of something despite of 2. Central pain pathways in the brain
evidence), Illusion (false idea or belief) - Effects: Obtundation (lessening of sensation due to anesthesia),
- When consumed together with alcohol: COCAETHYLENE (ethanol Coma, Respiratory arrest, Cardiac arrhythmias, Hypotension
+ cocaine) (secondary to histamine release)
o Ethanol becomes esterified with cocaine and blocks - Withdrawal from the drug is exceedingly difficult: Hypothermia,
reuptake of dopamine more effectively than cocaine Palpitations, Cold sweats, Nightmares
o Effect: Pronounced vasoconstriction of coronary arteries, - Treatment: Aside from naloxone, in chronic cases especially
Induces increased myocardial oxygen demand heroin addiction is treated with Methadone (partial agonist of
- Prolonged use of cocaine results in cardiotoxicity heroin)
o Progressive atherosclerosis and Constriction of coronary
arteries that can induce myocardial ischemia Amphetamines
- Passes readily across the placenta and also into the lactating - Street name: Eye opener, Lid poppers, Pep pills, Uppers, Hearts
mammary gland - Effects: Psychic stimulation, Excitability (euphoric states,increased
o Mental retardation, Delayed development, Strong drug mental activity, increased mental activity), Increased blood
dependence of newborns, Malformations in utero pressure (increased heart rate), Palpitations, Bronchodilation,
- Cocaine induces platelet aggregation and stimulates productionof Anxiety, Prolongs the effects of epinephrine and norepinephrine,
plasminogen activator inhibitor Talkativeness, Pallor, Tremulousness (voice is unsteady)
- Tests: - Patients may not sleep or eat
1. GC-MS (Gas-Chromatography Mass spectroscopy): up to 48 - Orgasm / ejaculation is difficult to achieve (Sexual marathon)
hrs after admin. - Suspiciousness paranoia producing unpredictable violent behavior
2. TLC (Thin layer chromatography): up to several hours - If fatigue occurs, user may sleep for 24 hours to 48 hours, then
Immunoassay: up to 24 - 36 hours eats ravenously
- Treatment: - Treatment: for Narcolepsy or Narcoleptic and attention deficit
1. Hyperexcitable states with cardiac symptoms (palpitations) = disorder
benzodiazepines
2. Antidepressants, including fluoroxetine (Prozac)
 Anorexic effect: - Barbiturates are depressants (sedatives or hypnotics)
- Fat-soluble; pass easily across the BBB
A. Amphetamines: trade name Dexedrine - Includes the following:
- Close resemblance to the adrenergic amines such as epinephrine o Phenobarbital—long lasting barbiturate used as an
and nor epinephrine (Sympathomimetic Effects) anticonvulsant as it reduces the excitability of rapidly firing
- Acute toxicity: Cardiovascular (flushing or pallor, tachypnea, neurons.
palpitation, tremor, labile pulse and blood pressure, Arrhythmia, o Pentobarbital—short acting
heart block, circulatory collapse, angina), Mental delirium, Acute - Toxic manifestations: depression, cyanosis, hypothermia,
psychotic syndromes, Acute intoxications hypotension, Cheyne-Stokes respiration
- Chronic usage: emotional ability, somnolence, loss of appetite,
occupational deterioration, mental impairment, social withdrawal Marijuana
o Trauma and ulcer of the tongue and lip: continuous chewing - Street name: pot, mary Jane, Mr, weed, grass, puff, nangga
and teeth-grinding movements - Psychoactive ingredient: ∆ - tetrahydrocannabinol
o Paranoid schizophrenia - From dried leaves and flowers of Indian Hemp (Cannabis sativa)
o Rare: aplastic anemia and fatal pancytopenia - Route of administration: Usually smoked but may be ingested
orally in brownies and on other foods
B. Methamphetamine (Shabu) - Death cases may be due to suicides
- Street name: Speed, ice, chalk, crystal, glass, Poor man's cocaine, - Detectable in urine for several days to a week after single
S, shabs, Siopao, sha. exposure, but in a heavy long term user, it may remain detectable
- Route of administration: ingestion, inhalation (chasing the for 21 — 30 days after last dose.
dragon), sniffing, injection, smoke , suppository (LEAST common) - Abstinence of 1 time user: can be detected up to 5 th day
- Effects: - Heavy users: 21 – 30 days (chronic)
o General: anxiety, irritability, irrational behavior - Users experience feeling of paranoia, sense of relaxation, mild
o Long term: psychosis similar to schizophrenia, difficulty in euphoria and relief of anxiety.
concentrating, loss of interest in sex - High doses may cause: anxiety, fear and paranoia, delusions,
o Physical: chest pain, irregular heartbeat, hypertension, depression, disorientation, hallucinations, confusion
convulsion, death
Psilocybin
C. Methylenedioxymethamphetamine (MDMA) / 3-4 MDMA:  Component of magic mushroom
- Street name: E, ecstacy, adam, XTC, lover's speed, essence,  Halucinogen
herbals
- "designer" hallucinogenic stimulant drug
- Half-life: 8 – 9 hours Toxic agents:
- Route of administration: Inhalation, Ingestion, Smoking - Acute toxicity: single short term exposure to the substance
- Synthetic drug, structurally related and derived from - Chronic toxicity: repeated exposure
amphetamine
- Effects: feeling of euphoria, heightens sexuality, expands Alcohol
consciousness without loss of control, fatal malignant - CNS depressant
hypothermia, seizures, tachycardia, DIC. - Causes disorientation, euphoria, confusion and may progress to
unconsciousness, paralysis and even death
Lysergic Acid Diethylamide (LSD) - Symptoms of alcohol intoxication begin when the concentration is
- Street name: Lucy in the sky of diamonds, wedding bells, acid, > 0.05% w/w (> 50 mg/dL blood alcohol)
white sugar, lightning, cubes, brain eaters.
- Route of administration:injection or oral administration Ethanol (grain alcohol)
- Effects: Visual hallucination (undulating vision), perceptual - Most commonly abused drugs
distortion, synesthesia (overflow of sensory input so that colors - Major metabolic pathway:
are "heard" and music becomes "palpable", papillary dilatation, - Readily absorbed in the Gil and diffuses easily in tissues
uterine contraction, panic reactions such as "bad trip" - The abuse causes acidosis through accumulation of ketones and
- Usual dosage: 1-2mcg/kg lactate and also through direct generation of hydrogen ions as
- Experience: begins = 1 hr after; peaks = 2-3 hrs; lasts = 8-12 his alcohol is oxidized
- Metabolized in the liver, excretion through bile - Chronic consumption: 50 g of ethanol per day for about 10 years
- Treatment: frequent reassurance, quiet and calm environment, - Accumulation of lipids in hepatocytes, Alcoholic hepatitis,
diazepam, Isolation (best treatment) Cirrhosis, Adds osmolality to the blood, Inhibit ADH
- Deaths are usually due to SUICIDES or ACCIDENTS

Phencyclidine (PCP)
- Street name: angel dust or angel hair, crystal super grass, killer
joints, ozone, wack, rocket fuel
- Effects: depression to euphoric state, violent behavior, auditory
and visual hallucination, vomiting, hyperventilation, tachycardia,
seizure, coma and death
- Slightly remain unchanged when eliminated in the urine
- Treatment: patient kept in isolation, in a dark, quiet room.
 Treatment with haloperidol (Haldol) results in sedation

Barbiturates:
- Street names: Lily, bala, downers, yellow jackets, blue heavens
- Major metabolite: Secobarbital
- Sedative hypnotic, Potentiate heroin
- Screening test: Immunoassay or TLC
- Confirmatory test: GC-MS
- Symptoms of abuse: slurred speech, slowing of mental functions,
constricted pupils CNS depression
- Pyrolysis product — burning of plastics
- Symptoms of intoxication: Blurred vision, Incoordination Slurred - Toxicity if through binding to iron (ferric and ferrous) -> hypoxia
speech, Coma, "hangover symptoms" —effects of acetaldehyde - Inhibition of electron transport and cell death
- Antidote for chronic intoxication: diazepam (for alcoholic mania) - Indication of toxicity: Odor of bitter almonds (breath)
- Specimen precaution: specimen must be capped all the time to - Toxic levels: > 2ug/mL (ingested in large quantities and absorbed
avoid evaporation of alcohol; alcohol-free skin cleanser must be in ionized form)
used instead of isopropanol (Benzalkonium chloride)
Arsenic
- Specimen: serum
- Common suicide agent
- Conversion of ethanol to acetaldehyde and acetyl coenzyme A by
- Ant poisons, rodenticides, paints and metal alloys
hepatic alcohol dehydrogenase
- Inhibits sulfhydryl enzymes; crosses the placenta
- Methods for testing: enzymatic (alcohol dehydrogenase reagent)
 Hair and nail ("MEES LINES") for long—term exposure
[PREFFERED], Gas-liquid chrom, and electrochemical oxidation
 Blood and urine for short — term exposure
- Common lab results: Elevated GGT, AST, AST/ALT ratio (de Ritis
- Indication of toxicity : Odor of garlic (breath and metallic taste)
ratio), HDL and MCV
- Acute fatal dosage: 120 mg (arsenic trioxide),30 ppm (arsenic gas)
- Fatal dose: 300 400 mL of pure alcohol consumed in < 1 hour
- Antidote: British anti-lewisite(BAL) arsenic rescue of affected cells
- Peak: within 1 hr after intake toxic blood level: > 400 mg/dL; > 500
- Test: Reinsch test, AAS
mg/dL (for hemodialysis)
Cadmium
Methanol (Wood alcohol) - Used in electroplating and galvanizing
- Common solvent and contaminant of homemade liquors - Pigment in paints and plastics
- Converted first to formaldehyde, then finally to formic acid in the - Poisoning can be a result from ingestion of acidic foods stored or
liver by alcohol dehydrogenase prepared in metal containers made up of cadmium
- Symptoms of intoxication: Frank blindness (ocular toxicity) and - Toxicity: destruction of epithelial cells in the lungs and
metabolic acidosis accumulation in renal tubules
- Preferred method: GC -MS - ltai-itai disease: severe osteomalacia and osteoporosis from long
- Screening test: computation of osmolal gap term consumption of cadmium contaminated rice
- Fatal dose: 60 - 250 mL - Half-life: 10-30 years
- Toxic blood level: > 50 mg/dL - Specimen: urine or whole blood
- Lab method: AAS
Isopropanol (Rubbing alcohol)
- Rapidly absorbed by the GIT Lead
- Metabolized by the hepatic alcohol dehydrogenase to acetone - Blocks delta aminolevulinic acid (ALA) synthetase, pyrimidine-5'-
- Symptoms of intoxication: CNS depression and hypertension nucleotidase, and Na-K---dependent ATPase
- Preferred method: gas chromatography - Source: paints, gasoline
- Antidote: activated charcoal - Mode of acquisition: ingestion or inhalation
- Fatal dose: 250 mL - Effects: anemia, birth defects, ADHD, low ICI
- Susceptible areas: CNS and PNS
Ethvlene glycol (1,2-ethanediol) - Toxicity: urinary ALA, free RBC protoporphyrin and basophilic
- Common constituent of hydraulic fluid and antifreeze stippling in RBCs
- Crystal of urine: calcium oxalate - Toxic dose: > 0.5 mg/day; fatal: > 70 ug/dL
- Converted to oxalic add and glycolic acid by hepatic alcohol - Chelation therapy: EDTA and dimercaptosuccinic acid (DMA)
dehydrogenase - Toxic effects: Lead palsy
- Symptoms of intoxication: Metabolic acidosis, Depressed - Vit D and heme synthesis interference
reflexes, Anuria, Necrosis, - Diminished integrity of RBC membrane
- Mode of treatment: inhibit the action of alcohol dehydrogenase - Combines with matrix of the bones (Half-life: 32 years)
- Indication of toxicity: deposition of calcium oxalate crystals in the - "wrist drop or foot drop" manifestation (peripheral neuropathy)
renal tubules - Labs:
- Major metabolite: glycolic acid (acute toxicity and death) o Whole blood: quantitative tests
- Preferred method: HPLC o Urine: recent exposure
o Morning urine for delta ALA: diagnosis of lead poisoning
- Fatal dose: 100 grams
o Serum or plasma should not be used
- Lab tests:
Carbon monoxide (CO) o Screening: Zinc protoporphyrin test (fluorometric test), ALAD (D -ALA
- Colorless, odorless, tasteless gas dehydratase test) — sensitive method
- Produced by incomplete combustion of carbon containing o In vivo x-ray fluorescence of bones — lead burden
substances like gasoline engines, organic materials in fire and o AAS and Inductively coupled plasma emission spectrophotometry
cigarette smoke (ICP- MS)
- Binds with heme Mercury
- Higher affinity to hemoglobin transport than oxygen - Binds with sulfhydryl proteins (change in structure and functions)
- Color of Blood: Cherry Red (acute) - Enzyme inhibitor
- Stimulates production of nitrous oxide -> hypotension and - Forms: elemental or metallic, mercurous, mercuric and alkyl
neurologic changes - Acquisition: inhalation, skin absorption, and ingestion
- Major toxic effect: Tissue hypoxemia or hypoxia - Toxic effects: General: organ dysfunction, Elemental: pink disease
- Toxic level: 20% of carbon monoxide (acrodyna) and erethism, Alkyl: congenital Minimata disease
- Indication for acute toxicity: Cherry Red (also on skin) - Samples: whole blood and 24-hr urine
- Sample for testing: EDTA whole blood - Route of excretion: bile
- Definitive method for testing: cooximetry (carboxyhemoglobin) - Method: reinsch test; simple test to detect large amounts of
mercury in urine (also for antimony, bismuth and selenium);
Cyanide (Metals) Pesticides
- Common suicidal agent, - Includes the organophosphates and carbamates
- Can be solid, gas, or in solution - Act by inhibiting the action of acetylcholinesterases, so
- Super toxic substance (fast acting) acetylcholine accumulates at the neuromuscular junction
- Death may occur less than an hour
- Components of insecticides and rodenticides PandaMT13

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