Chapter 7 Drugs

1. Chapter 7Drugs “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

2. Drugs Students will learn: • 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. Kendall/Hunt Publishing Company

3. Drugs Students will be able to: • 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. Kendall/Hunt Publishing Company

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. Kendall/Hunt Publishing Company

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. Kendall/Hunt Publishing Company

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 Kendall/Hunt Publishing Company

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 Kendall/Hunt Publishing Company

8. Identification of Drugs • PDR—Physicians’ Desk Reference • Field Tests—presumptive tests • Laboratory Tests—conclusive tests Kendall/Hunt Publishing Company

9. Blood Urine Hair Gastric Contents Bile Liver tissue Brain tissue Kidney tissue Spleen tissue Vitreous Humor of the Eye Human ComponentsUsed for Drug Analysis Kendall/Hunt Publishing Company

10. 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. Kendall/Hunt Publishing Company

11. 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 Drug Identification Kendall/Hunt Publishing Company

12. 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 Presumptive Color Tests Kendall/Hunt Publishing Company

13. 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. Kendall/Hunt Publishing Company

14. Types of Chromatography • Paper • Thin Layer (TLC) • Gas (GC) • Pyrolysis Gas (PGC) • Liquid (LC) • High Pressure Liquid (HPLC) • Column Kendall/Hunt Publishing Company

15. Paper Chromatography • Stationary phase—paper • Mobile phase—a liquid solvent Capillary action moves the mobile phase through the stationary phase Kendall/Hunt Publishing Company

16. 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 Kendall/Hunt Publishing Company

17. 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). Kendall/Hunt Publishing Company

18. Phases 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 Gas Chromatography Kendall/Hunt Publishing Company

19. 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). Kendall/Hunt Publishing Company

20. Spectroscopy • Spectroscopy—the interaction of electromagnetic radiation with matter. • Spectrophotometer—an instrument used to measure and record the absorption spectrum of a chemical substance. Kendall/Hunt Publishing Company

21. Spectrophotometry Components • 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 Kendall/Hunt Publishing Company

22. 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 Kendall/Hunt Publishing Company

23. Mass Spectrometry Gas chromatography has one major drawback, it does not give a specific identification. Mass spectrometry cannot separate mixtures or provide specific identification. By combining the two (GCMS), constituents of mixtures can be specifically identified. Kendall/Hunt Publishing Company

24. 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. Kendall/Hunt Publishing Company

25. Mass Spectra Each molecular species has its own unique mass spectrum. Kendall/Hunt Publishing Company

26. 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 Kendall/Hunt Publishing Company

27. 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. Kendall/Hunt Publishing Company

28. 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. Kendall/Hunt Publishing Company