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Drug Analysis
Drug Analysis
Drug Analysis
Pharmacologically
classified as an
analgesic
Central Nervous
System (CNS)
Depressants
Popular drugs –
heroin, morphine,
codeine, methadone
and propoxyphene
Hallucinogens
Marijuana
Derived from the plant
Cannabis
Hashish – concentrated
Sinsemilla – unfertilized
flowering tops of the
female Cannabis plant
Active ingredient is THC
Potency is normally 4-5%
Simsemilla averages 6-12%
Liquid hashish averages 8-
22%
Potential medical uses
Hallucinogens
LSD – derived from ergot, a fungus of
certain grains and grasses
Powerful drug
Visual hallucinations, changes in moods,
anxiety, tension, etc
Flashbacks possible
Phencyclidine (PCP)
Human response unpredictable
Dangerous drug – paranoia and
violence possible
Schizophrenic behavior possible
days after use
Methylenedioxymethamphetamine
(aka MDMA or Ecstasy)
Originally patented as appetite
suppressant
Severe adverse reactions, including
fatal side effects
Depressants
Alcohol (aka ethanol, ethyl alcohol, booze, etc.)
Central nervous system depressant
Legalized and most widely used drug
A common effect is impairment
Legal blood alcohol level in Oklahoma
is 0.10%, or 100 mg/dL
Barbiturates
All are derivatives of barbituric acid
Big 5: amobarbital, secobarbital,
phenobarbital, pentobarbital and butalbital
Methaqualon
. Tranquilizers
Major players: reserpine, chlorpromazine,
meprobamate, chlordiazepoxide, diazepam
Inhalants
Volatile organic solvents – toluene, naphtha,
gasoline among others
Initial exhilaration and euphoria followed by
impaired judgment, drowsiness and stupor
Danger of liver, heart and brain damage
Stimulants
Amphetamines
Initial feeling of well-being and
alertness followed by fatigue and a
loss of appetite
Amphetamine, methamphetamine and
“ice” (crystal meth) are favorites
Phenmetrazine and phendimetrazine
have similar properties
Cocaine
First used medically by Freud in
Europe
Medical use is now limited
Extracted from the leaves of coca plant
(Erythroxylon coca)
“Crack” cocaine is the drug of choice
Cocaine produces the strongest
psychological compulsions for
continued use
Drugs: Organized by Control Laws
Federal law restricting the manufacture and distribution
of dangerous substances
The U.S. Attorney General has the authority to change
the schedules
The criminal penalties associated with this law are
greatest with schedules I and II.
Controlled Substances Act
Schedule I
No medical use
High potential for abuse
Heroin, LSD, methaqualone and marijuana - High potential for abuse
Cocaine, opiates, PCP, amphetamines, methadone and fast-acting barbiturates
Schedule II
Accepted medical use
Potential for psychological or physical dependence
Cocaine, opiates, PCP, amphetamines, methadone and fast-acting barbiturates
Schedule III
Less potential for abuse than schedules I and II
Currently accepted medical use
Potential for low or moderate physical dependence or high psychological
dependence
Anabolic steroids, some codeine preparations and some barbiturate
preparations (phenobarbital not included)
Controlled Substances Act
Schedule IV
Low potential for abuse relative to schedule III drugs
Currently accepted medical use
Relatively low limited dependence risk
Propoxyphene, phenobarbital, meprobamate, diazepam and
chlordiazepoxide
Schedule V
Low abuse potential
Medical use
Less potential for producing dependency
Certain opiate drug mixtures that contain non-narcotic medicinal
ingredients
Designer drugs
Can be placed under schedule I
Fentanyl analogues
Characterization
Color tests - often termed presumptive tests
Marquis – purple color in presence of opiates and orange-
brown in presence of amphetamines
Dillie-Koppanyi – violet-blue color in presence of
barbiturates
Duquenois-Levine – purple color in presence of marijuana
Van Urk – blue-purple color in presence of LSD
Scott – blue color in presence of cocaine
Characterization
UV and IR Spectroscopy
GC-MS
Note that the neutral classification Alkaloids are generally derived
includes those drugs that have no from plants while the nonalkaloids
ionizable center and those which are are syhtthetic or semisynthetic
amphoteric
Morphine
Dia(acetyl)morphine - opiod,
Methyl Salicylate - Aspirin amphoteric
active ingredient in heroin
pKa = 3.5 pKa = 8
HPLC Separation of Methamphetamines
Column: C8, 4.6 x 150 mm
Mobile Phase:
85% 25 mM phosphate buffer
15% ACN
Temperature: 35°C
Detection: 254 nm
2. Repeat the calculation in Question 5 for caffeine, a weak base with a of 0.6.
3. Diazepam tablets are supplied in 2-, 5-, and 10-mg increments. Suppose several tablets
are received in a laboratory as evidence and, using the Physician’s Desk
Reference, an analyst was able to tentatively identify them as Valium®, 10 mg. Suppose
further that you learn that the tablets also contain anhydrous lactose,
starches, dyes, and calcium stearate. Describe a method for isolating the active ingredient
from fillers, using a LLE scheme. Justify and explain each step of
the method.
4. Quinine is a dibasic molecule with of 5.1 and 9.7. It is encountered as a diluent (cutting
agent) for heroin. To extract quinine from an aqueous solution, what pH should be used
and why?