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Examination of Firearms Review: 2007 to 2010 - Interpol

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quantitation <strong>of</strong> common drugs <strong>of</strong> abuse in oral fluid, collected with Quantasil<br />

oral fluid collection kits, was reported with LODs/LOQs being 2-10 ng/mL [41].<br />

A confirmational analysis <strong>of</strong> drugs, including morphine, cocaine,<br />

benzoylecgonine, and amphetamines in oral fluid by LC-MS was also reported.<br />

300 µL <strong>of</strong> oral fluid is required for the testing, with LODs <strong>of</strong> 0.5 – 1 ng/mL [33].<br />

That the window <strong>of</strong> detection <strong>of</strong> drugs in oral fluid reflects the corresponding<br />

window in blood suggests that oral fluid is a specimen <strong>of</strong> choice for roadside<br />

testing. However, oral fluid/blood ratios vary from drug <strong>to</strong> drug, from person <strong>to</strong><br />

person, and even intra-individually, posing challenges in interpretation <strong>of</strong> the<br />

results for oral fluid. Blood (B) and oral fluid (OF) samples collected from<br />

drivers suspected <strong>of</strong> DUID in Belgium, Germany, Finland, and Norway for the<br />

ROSITA-2 project were used <strong>to</strong> study the relationship between the oral fluid<br />

and the blood concentrations <strong>of</strong> drugs <strong>of</strong> abuse [42]. The ratios found in this<br />

study were comparable with those that were published previously, but the<br />

range was wider. The median <strong>of</strong> the OF:B ratios <strong>of</strong> basic drugs such as<br />

amphetamines, cocaine, and opiates were 4-13, 22, and 2-10 respectively.<br />

The ratios for benzodiazepines were very low (median OF:B ratio: 0.02-0.1)<br />

while that for THC was 15. Several methods for estimating the prevalence <strong>of</strong><br />

high blood concentrations <strong>of</strong> THC and amphetamine in a population <strong>of</strong> drug<br />

users by analysing their OF suggested that dividing the drug concentration in<br />

OF by the OF/B regression coefficient gives an acceptable estimation <strong>of</strong> high<br />

blood drug concentrations, which may give valuable additional information on<br />

possible drug impairment [43]. The presence <strong>of</strong> THC in blood is usually<br />

interpreted as an indica<strong>to</strong>r for recent drug use. However, a study <strong>of</strong> chronic<br />

cannabis users over 7 days <strong>of</strong> continuous moni<strong>to</strong>red abstinence showed that<br />

substantial whole blood THC concentrations (0.3 ± 0.7 ng/mL) persisted<br />

multiple days after drug discontinuation in heavy chronic cannabis users [44]. A<br />

comparison <strong>of</strong> the impairment <strong>of</strong> driving-relevant skills by alcohol or cannabis<br />

suggested that a THC concentration in serum <strong>of</strong> 7-10 ng/mL is correlated with<br />

an impairment comparable <strong>to</strong> that caused by BAC <strong>of</strong> 0.05%. The per se limits<br />

for THC in blood appear <strong>to</strong> be the most effective approach <strong>to</strong> differentiating<br />

drivers who are impaired by cannabis use from those who are no longer under<br />

the influence [45]. The relationship between blood zopiclone and zolpidem<br />

concentrations and driving impairment was assessed by a clinical test, and the<br />

impairment was compared in that with a group <strong>of</strong> drivers with suspected<br />

alcohol-related impairment [46]. It is concluded that the percentage <strong>of</strong> impaired<br />

drivers with blood zopiclone concentrations above 130 µg/L roughly<br />

620

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