04.04.2013 Views

FORENSIC TOXICOLOGY - Bio Medical Forensics

FORENSIC TOXICOLOGY - Bio Medical Forensics

FORENSIC TOXICOLOGY - Bio Medical Forensics

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

esterification of cocaine with ethyl alcohol when used simultaneously.<br />

Anhydroecgonine methyl ester (AEME) is a unique metabolite of<br />

smoked cocaine, and anhydroecgonine ethyl ester (AEEE) has been<br />

identified in cocaine smokers who also use ethyl alcohol. A method has<br />

been developed for the detection of and quantiation of COC, HOBE,<br />

AEME, AEEE, NC, CE, and BE in urine at low concentrations.<br />

Sixty-eight randomly selected previously confirmed BE positive by<br />

GC-Ms were collected from May 19 th to 22 nd and June 20 th to 27 th .<br />

Samples were extracted using SPE and 30uL of the reconstituted extract<br />

was injected. Chromatographic separation was achieved using a gradient<br />

consisting of Mobile phase A [20mM ammonium formate (pH = 2.7)]<br />

and Mobile phase B [50%/50% methanol/acetonitrile], and an XDB-C8,<br />

1.8micron, 2.1x50mm column, with a flow rate of 270 ul/min.<br />

Concentrations were calculated by comparing the drug peak area with<br />

the internal standard peak-area. The ratio was plotted against a standard<br />

curve.<br />

The assay displayed linearity from 1.0m- 1000 ng/mL for all<br />

analytes. Between-run CVs were 1.0 ng/mL.<br />

Standard surveys to determine methods of cocaine use rely on<br />

individual responses to survey questions, and assumes that users<br />

responses are honest. We report here on a sensitive method to identify<br />

cocaine metabolites at concentrations as low as 1.0 ng/mL. Because of<br />

the unique derivation of some of the metabolites, the pattern of the<br />

metabolites makes it possible to determine the user’s method of cocaine<br />

ingestion. This assay could be used to validate or challenge current<br />

survey techniques.<br />

Cocaine, Cocaine Metabolites, LC-MS/MS<br />

K36 Opiate Withdrawal and Adulterated CNS<br />

Depressant Drug Impaired Driving: Case<br />

Interpretation and Overcoming Motions<br />

to Suppress<br />

Michael Wagner, PhD*, State Department of Toxicology, Indiana<br />

University, 550 West Sixteenth Street, Indianapolis, IN 46202<br />

After attending this presentation, attendees will understand the key<br />

medical legal issues addressed when evaluating impaired driving<br />

resulting from opiate addiction. Case history, self reporting, biological<br />

samples, analytical test results, relevant case law, and strategies<br />

challenging motions to suppress will be discussed. In addition, the<br />

opposing conclusions from the expert witnesses will be presented.<br />

This presentation will impact the forensic community by<br />

interpreting DUID cases involving impairment when only trace<br />

analytical test results are available.<br />

On March 7th at 1445 hours, police are notified of a collision<br />

involving two vehicles (vehicle #1 a 1998 Nissan Frontier (pickup truck)<br />

and vehicle #2 a 1987 Volvo 740). The weather was clear and dry.<br />

Vehicle #2 was traveling eastbound and made a left hand turn (northerly)<br />

when it was struck broadside by vehicle #1 that was traveling<br />

westbound. Vehicle #1 driven by a 47-year-old male had violated a red<br />

traffic control device just prior to this collision. As a result of this<br />

accident, two males ages 17 and 34 occupying vehicle #2 had been<br />

fatally injured.<br />

Scene evaluation of the driver for vehicle #1 reveals the subject<br />

claims to have been reaching down for a water bottle and taking his<br />

attention off the roadway. The subject made statements at the scene to<br />

police officers and medical personnel that he was a heroin addict and had<br />

ingested three Klonopin® prescription pills approximately 09:00 –<br />

09:30. He crushed two of the pills and snorted them, and then he<br />

ingested the third. Subject claimed to have eaten very little in the past<br />

two days (two bowls of cereal the previous day) and nothing that day<br />

(body height and weight were 6’1” and 135 pounds). In addition, the<br />

subject claimed to be in withdrawal with his last use of Heroin having<br />

been on March 5 th . The subject admitted to be in route to purchasing<br />

more Heroin and having $2,500 dollars in cash. Multiple blood samples<br />

were collected and indicated the presence of trace parent cocaine and<br />

metabolite, trace clonazepam, while urine test results confirmed the<br />

presence of morphine and oxycodone in addition to parent cocaine and<br />

benzoylecognine.<br />

DUID, Opiate Impairment, Benzodiazepines<br />

K37 Prescription Drugs, Poor Driving, DRE<br />

Evaluation…and a Surprising Verdict –<br />

A DUID Case Study<br />

Laura J. Liddicoat, BS*, Toxicology Section - WSLH, 2601 Agriculture<br />

Drive, PO Box 7996, Madison, WI 53707-7996<br />

After attending this presentation, attendees will have a greater<br />

understanding of drug interpretation, prosecutor preparation, and<br />

effective expert witness testimony for prescription drug impaired driving<br />

cases.<br />

This presentation will impact the forensic community by<br />

influencing toxicologists who are involved with suspected DUID cases<br />

by enhancing their understanding of the challenges to interpretive issues.<br />

For drugs other than alcohol, interpretation of drug concentrations<br />

and effects on safe driving ability is extremely complex. The<br />

toxicologist must consider drug pharmacology, pharmacokinetics, drug<br />

interactions, medical information, and research findings and apply them<br />

to the individual case scenario. This information must then be presented<br />

to the attorneys during preparation for the trial.<br />

The case study that will be presented involves several drugs that can<br />

severely affect driving abilities. The drugs include oxycodone (at a<br />

potentially toxic concentration of 530 ng/mL), diazepam, nordiazepam,<br />

cyclobenzaprine and citalopram. Poor driving was observed by a citizen<br />

driver, reported to law enforcement, and documented by the arresting<br />

State Patrol Officer. A Drug Recognition Expert (DRE) was called to the<br />

scene and conducted an evaluation of the driver. The DRE concluded<br />

that he was impaired and under the influence of a CNS Depressant and<br />

Narcotic Analgesics.<br />

At trial the driver alleged that he was able to ingest several<br />

oxycodone pills while in custody and prior to the blood sample<br />

collection. Even though this case had all the required elements for a<br />

DUID conviction, the first hearing resulted in a mistrial and was<br />

subsequently retried. The full case will be presented with emphasis<br />

given to drug interpretation, pharmacokinetics, prosecutor preparation,<br />

and effective expert witness testimony.<br />

Drugs, Driving, Impairment<br />

K38 Driving Under the Influence of<br />

Methamphetamine in the City &<br />

County of San Francisco, California<br />

Nikolas P. Lemos, PhD*, and Ann M. Gordon, MA, San Francisco Office<br />

of the Chief <strong>Medical</strong> Examiner, 850 Bryant Street, Hall of Justice, North<br />

Terrace, San Francisco, CA 94103; and Preston J. Wong, BS, 5013<br />

Hummingbird Lane, Plano, TX 75093<br />

After attending this presentation, attendees will have a better<br />

understanding of the signs and symptoms often observed in drivers<br />

driving under the influence of methamphetamine, the measured<br />

concentrations of the drug in the drivers’ blood specimens, and the<br />

73 * Presenting Author

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!