14.01.2015 Views

SOFT 2004 Meeting Abstracts - Society of Forensic Toxicologists

SOFT 2004 Meeting Abstracts - Society of Forensic Toxicologists

SOFT 2004 Meeting Abstracts - Society of Forensic Toxicologists

SHOW MORE
SHOW LESS

Create successful ePaper yourself

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

P21 <br />

"STUDENT ON ALPHA-METHYLTRYPTAMINE DISCOVERS mE SECRET OF THE<br />

UNIVERSE.•• AND DIES"<br />

Diane M. Boland*, Wilmo Andollo, George W. Hime, and William L. Hearn, Dade County Medical<br />

Examiner, Number One on Bob Hope Rd, Miami, FL, 33136<br />

Alpha-methyltryptamine (AMT) is a synthetic indole analog <strong>of</strong> amphetamine initially investigated as a<br />

monoamine oxidase inhibitor. In the 1960s, the Soviet Union marketed AMT as an antidepressant under<br />

the name <strong>of</strong>lndopan. During the same period, the Upjohn Company studied the alpha-ethylated analog for<br />

use as a commercial antidepressant known as Monase, but found it to be <strong>of</strong> little medicinal value.<br />

Although clinical use <strong>of</strong> AMT is obsolete today, recreational use has gained popularity due to its intense<br />

hallucinogenic properties lasting up to 16 hours. To illustrate recreational use <strong>of</strong> AMT in the 1960s,<br />

Alexander Shulgin in his book Tihkal, references the author Ken Kesey and his experiences with AMT and<br />

other hallucinogenic drugs.<br />

Today, AMT is recognized as a powerful psychedelic drug among high school and college-aged men and<br />

women who may have experienced the effects <strong>of</strong> other hallucinogenic amphetamines. Its popularity is<br />

partly due to the legality and availability <strong>of</strong> AMT for purchase via the Internet prior to April 2003.<br />

Emergency designation <strong>of</strong> AMT as a Schedule 1 controlled substance by the Drug Enforcement<br />

Administration occurred shortly after the Miami-Dade Medical Examiner reported the death <strong>of</strong> a 22 yearold<br />

college student who ingested a large amount <strong>of</strong> AMT. Prior to death, the deceased advised his<br />

roommate that he was ''taking hallucinating drugs" and as a result had "discovered the secret <strong>of</strong> the<br />

universe". The roommate reported that the deceased was shaking and sweating pr<strong>of</strong>usely. Approximately<br />

12 hours later, the roommate discovered the deceased lying in bed unresponsive. An empty Igram vial <strong>of</strong><br />

AMT was recovered from the scene and sent to the Toxicology Laboratory. An autopsy by the Medical<br />

Examiner did not reveal any significant gross findings <strong>of</strong> any organs, and no evidence <strong>of</strong>traumatic injury.<br />

Initial screening <strong>of</strong> urine by enzyme-multiplied immunoassay technique was positive for amphetamines,<br />

and the basic drug blood screen detected a small peak later identified by mass spectrometry as AMT. For<br />

quantitation, AMT was isolated using solid phase extraction, derivatized with pentafluoropropionic<br />

anhydride, and analyzed using gas chromatography/mass spectrometry. Ions monitored for AMT included<br />

mlz 276, 303, and 466. Quantitative analysis was based upon mJz 276 for AMT and mJz 306 for the<br />

internal standard 5-methoxy-alpha-methyltryptamine. A linear calibration curve from 50 to 500ng/mL was<br />

used to calculate· the concentration <strong>of</strong> AMT in the samples and controls. Blood, tissue, and gastric<br />

specimens were diluted to bring the observed concentration within the limits <strong>of</strong> the standard curve. Matrix<br />

matched controls were extracted and analyzed with each run. Postmortem blood revealed 2.0mg/L, gastric<br />

contents 9.6mg total, liver 24.7mgikg, and brain 7.8mgikg.<br />

Keywords: Alpha-methyltryptamine, 5-Methoxy-alpha-methyltryptamine, hallucinogens<br />

Page 356

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

Saved successfully!

Ooh no, something went wrong!