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Examination of Firearms Review: 2007 to 2010 - Interpol

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ains, with very low concentrations in femoral venous blood (738 mg/kg vs. 5<br />

mg/L and 1008 mg/kg vs. 228 mg/L) and other postmortem specimens [476].<br />

Toxicological analysis <strong>of</strong> a fatality involving a woman who ingested an<br />

unknown quantity <strong>of</strong> a pine oil-containing product was reported [ 477 ].<br />

Postmortem blood, urine, and s<strong>to</strong>mach content levels <strong>of</strong> 1-alpha-terpineol<br />

analyzed by GC-MS were 276 mg/L, 0.5 mg/L, and 4.0 g/<strong>to</strong>tal contents,<br />

respectively, and isopropanol levels analysed by GC-FID were 730 mg/dL, 20<br />

mg/dL, and 1000 mg/dL, respectively, with no ace<strong>to</strong>ne detected.<br />

3.5.1.2 Abused drugs<br />

A study on the gender differences in pharmacokinetics for opiates using male<br />

and female Wistar rats showed that the maximal contents <strong>of</strong> opiates in blood <strong>of</strong><br />

both genders were found in the second measurement time (15 min), and faster<br />

distribution <strong>of</strong> opiates from blood <strong>to</strong> brain in the female compared <strong>to</strong> male rats<br />

[ 478 ]. Human subjects, who received 16 mg buprenorphine and 4 mg<br />

naloxone, were found <strong>to</strong> have naloxone detected up <strong>to</strong> 2 h in three subjects<br />

and up <strong>to</strong> 4 h in one subject, with mean maximum concentration was 0.139 ±<br />

0.062 ng/mL. In urine samples taken 24 h after administration, about 55% <strong>of</strong><br />

the daily dose was excreted in urine in either conjugated or unconjugated<br />

forms <strong>of</strong> naloxone and nornaloxone [479]. There has been an increased<br />

awareness <strong>of</strong> illicit opiate abusers using the narcotic oxymorphone (Opana) by<br />

inhalation. Two oxymorphone-involved fatalities were analyzed using GC-MS.<br />

Concentrations <strong>of</strong> oxymorphone in blood samples <strong>of</strong> the deceased were 0.05<br />

mg/L and 0.12 mg/L, respectively [480].<br />

A study examining the plasma pharmacokinetics <strong>of</strong> MDMA and metabolites<br />

using controlled oral administration <strong>of</strong> MDMA in young adults found that the<br />

mean maximum plasma concentrations <strong>of</strong> 162.9 ± 39.8 and 171.9 ± 79.5<br />

ng/mL were observed for MDMA and HMMA, respectively, at low dose (1.0<br />

mg/kg), and that the mean half-lives <strong>of</strong> MDMA, and HMMA were approximately<br />

7 <strong>to</strong> 8 hours, and 11.5 <strong>to</strong> 13.5 hours, respectively [481]. Three cases <strong>of</strong> MA<br />

related fatalities were reported [482,483,484]. In one case, about 3 g <strong>of</strong> MA<br />

was swallowed, the MA concentration in the hospital blood taken<br />

approximately 12 h after ingestion was 3.0 mg/L, and that in the femoral blood<br />

from au<strong>to</strong>psy was 30 mg/L [482]. The other two cases involved MA body<br />

packers that were believed <strong>to</strong> be poisoned due <strong>to</strong> MA leakage from the<br />

packages in<strong>to</strong> the s<strong>to</strong>mach. The MA concentration was found <strong>to</strong> be 8.6 mg/L in<br />

plasma 17 h before death, and 63.5 mg/L in the postmortem cardiac blood in<br />

677

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