Chapter 5

Drugs“Having sniffed the dead man’s lips, I detected a slightly sour smell, and I came to the conclusion that he had

poison forced upon him.”

—Sherlock Holmes, in Sir Arthur Conan Doyle’s

A Study in Scarlet

Chapter 5 2

Drugs

How to apply deductive reasoning to a series of analytical data.

The limitations of presumptive (screening) tests.

The relationship between the electromagnetic spectrum and spectroscopic analysis.

The dangers of using prescription drugs, controlled substances, over-the-counter medications, and illegal drugs.

Students will learn:

Chapter 5 3

Drugs

Chemically identify illicit drug types.

Classify the types of illicit drugs and their negative effects.

Discuss the federal penalties for possession and use of controlled substances.

Explain the need for confirmatory tests.

Students will be able to:

Chapter 5 4

Drugs

Describe IR, UV-VIS spectroscopy, and GC-MS

Present and interpret data with graphs.

Use the Physicians’ Desk Reference (PDR) to identify pills.

Use technology and mathematics to improve investigations and communications.

Chapter 5 5

Drugs and Crime

A drug is a natural or synthetic substance designed to affect the subject psychologically or physiologically.

“Controlled substances” are drugs that are restricted by law

Controlled Substances Act is a law that was enacted in 1970; it lists illegal drugs, their category and their penalty for possession, sale or use.

Chapter 5 6

Controlled Substances Act

Schedule I—high potential for abuse; no currently acceptable medical use in the US; a lack of accepted safety for use under medical supervision

Schedule II—high potential for abuse; a currently accepted medical use with severe restrictions; abuse may lead to severe psychological or physical dependence

Schedule III—lower potential for abuse than the drugs in I or II; a currently accepted medical use in the US; abuse may lead to moderate physical dependence or high psychological dependence

Schedule IV—low potential for abuse relative to drugs in III; a currently accepted medical use in the US; abuse may lead to limited physical or psychological dependence relative to drugs in III

Schedule V—low potential for abuse relative to drugs in IV; currently accepted medical use in the US; abuse may lead to limited physical or psychological dependence relative to drugs in IV

Chapter 5 7

Examples of Controlled Substances and Their Schedule Placement

Schedule I—heroin (diacetylmorphine), LSD, marijuana, ecstasy (MDMA)

Schedule II—cocaine, morphine, amphetamines (including methamphetamines), PCP, Ritalin

Schedule III—intermediate acting barbiturates, anabolic steroids, ketamine

Schedule IV—other stimulants and depressants including Valium, Xanan, Librium, phenobarbital, Darvon

Schedule V—codeine found in low doses in cough medicines

Chapter 5

Honors Forensics March 4, 2013

Congratulations to the Science Olympiad team!

1. Walter Payton

2. Lane Tech

3. Jones

4. VON STEUBEN

5. Alcott

6. Whitney Young

8

Chapter 5 9

Identification of Drugs

PDR—Physicians’ Desk Reference

Field Tests—presumptive tests

Laboratory Tests—conclusive tests

Chapter 5 10

Human ComponentsUsed for Drug Analysis Blood

Urine

Hair

Gastric Contents

Bile

Liver tissue

Brain tissue

Kidney tissue

Spleen tissue

Vitreous Humor of the Eye

Chapter 5 11

Physicians’ Desk Reference

PDR—a physicians’ desk reference is used to identify manufactured pills, tablets and capsules. It is updated each year. This can sometimes be a quick and easy identifier of the legally made drugs that may be found at a scene. The reference book gives a picture of the drug, whether it is a prescription, over the counter, or a controlled substance; as well as more detailed information about the drug.

Chapter 5 12

Drug Identification

Screening or presumptive tests Spot or color tests Microcrystalline test—

a reagent is added that produces a crystalline precipitate which is unique for a certain drug.

Chromatography

Confirmatory tests Spectrophotometry

Ultraviolet (UV) Visible Infrared (IR)

Mass spectrometry

Chapter 5 13

Presumptive Color Tests

Marquis—turns purple in the presence of most opium derivatives and orange-brown with amphetamines

Dillie-Koppanyi—turns violet-blue in the presence of barbiturates

Duquenois-Levine—turns a purple color in the presence of marijuana

Van Urk—turns a blue-purple in the presence of LSD

Scott test—color test for cocaine, blue

Chapter 5

Testing Pain Relievers Lab

® Two sets of procedure per table

( class set )

You need to MAKE a data table to turn in ( one per group )

At the end of the period, turn in your data table with group names and your procedure sheets ( with Nothing written on them )

14

Chapter 5 15

Chromatography

A technique for separating mixtures into their components

Includes two phases—a mobile one that flows past a stationary one.

The mixture interacts with the stationary phase and separates.

Chapter 5 16

Types of Chromatography

Paper Thin Layer (TLC) Gas (GC) Pyrolysis Gas (PGC) Liquid (LC) High Pressure Liquid (HPLC) Column

Chapter 5 17

Paper Chromatography

Stationary phase—paper

Mobile phase—a liquid solvent

Capillary action moves the mobile phase through the stationary phase

Chapter 5 18

Thin Layer Chromatography

Stationary phase— a thin layer of coating (usually alumina or silica) on a sheet of plastic or glass

Mobile phase—a liquid solvent

Chapter 5 19

Retention Factor (Rf) This is a number that represents

how far a compound travels in a particular solvent

It is determined by measuring the distance the compound traveled and dividing it by the distance the solvent traveled.

If the Rf value for an unknown compound is close to or the same as that for the known compound, the two compounds are likely similar or identical (a match).

Chapter 5 20

Gas ChromatographyPhases Stationary—a solid or a

viscous liquid that lines a tube or column

Mobile—an inert gas like nitrogen or helium

Analysis Shows a peak that is

proportional to the quantity of the substance present

Uses retention time instead of Rf for the qualitative analysis

Chapter 5 21

Uses of Gas Chromatography

Not considered a confirmation of a controlled substance

Used as a separation tool for mass spectroscopy (MS) and infrared spectroscopy (IR)

Used to quantitatively measure the concentration of a sample. (In a courtroom, there is no real requirement to know the concentration of a substance. It does not affect guilt or innocence).

Chapter 5 22

Spectroscopy Spectroscopy—the interaction of

electromagnetic radiation with matter. Spectrophotometer—an instrument used to

measure and record the absorption spectrum of a chemical substance.

Chapter 5 23

SpectrophotometryComponents

A radiation source A frequency selector A sample holder A detector to convert electromagnetic

radiation into an electrical signal A recorder to produce a record of the signal

Types Ultraviolet Visible Infrared

Chapter 5 24

Infrared Spectometry

Material absorbs energy in the near-IR region of the electromagnetic spectrum.

Compares the IR light beam before and after passing through a transparent sample.

Result—an absorption or transmittance spectrum Gives a unique view of the substance; like a fingerprint

Chapter 5 25

Mass Spectrometry

Gas chromatography has one major drawback, it does not give a specific identification. Mass spectrometry cannot separate mixtures. By combining the two (GCMS), constituents of mixtures can be specifically identified.

Chapter 5 26

Mass Spectrometry

In a mass spectrometer, an electron beam is directed at sample molecules in a vacuum chamber. The electrons break apart the sample molecules into many positive charged fragments. These are sorted and collected according to their mass-to-charge ratio by an oscillating electric or a magnetic field.

Chapter 5 27

Mass Spectra

Each molecular species has its own unique mass spectrum.

Chapter 5 28

IR Spectrophotometry andMass Spectrometry

Both work well in identifying pure substances.

Mixtures are difficult to identify in both techniques

Both are compared to a catalog of knowns

Chapter 5 29

People of Historical Significance

Arthur Jeffrey Dempster was born in Canada, but studied and received his PhD from the University of Chicago. He began teaching physics there in 1916. In 1918, Dempster developed the first modern mass spectrometer. His version was over 100 times more accurate than previous ones developed, and established the basic theory and design of mass spectrometers that is still used to this day.

Chapter 5 30

People of Historical Significance

Francis William Aston was a British physicist who won the 1922 Nobel Prize in Chemistry for his work in the invention of the mass spectrograph. He used a method of electromagnetic focusing to separate substances. This enabled him to identify no fewer than 212 of the 287 naturally occurring elemental isotopes.