Page 28 - Advances in Forensic Applications of Mass Spectrometry - Jehuda Yinon
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                             d -tetrahydrocannabivarin, was found to be a marker for marijuana or a
                             related product use. 193

                             1.4.1.1.4  Opioid (Narcotic) and Other Potent Analgesics.  Opioid anal-
                             gesics, often called narcotics, are widely used to reduce severe pain, especially
                             in a postoperative state and in the final state of cancer diseases. These are
                             also abused because of their euphoriant and anxiolytic effects. While opioid
                             medicaments are usually misused by medical staff, heroin is widely abused
                             by  drug addicts. If heroin is not available the addicts often take opioid
                             medicaments. For legal reasons, the use of heroin must analytically be dif-
                             ferentiated from an intake of other opioids. Therefore, 6-monoacetylmor-
                             phine, the only heroin specific metabolite, must be detected in biosamples.
                             Several papers have been published on the detection of 6-monoacetylmor-
                             phine, employing SPE or LLE and derivatization by TFA, PFP, propionyla-
                             tion, or by TMS. 1
                                Screening procedures have been described for the detection of most of
                             the opioids and other potent analgesics after acid or enzymatic hydrolysis
                             with LLE or SPE at pH 8 to 9, followed by TMS or AC. 1,194–197  The latter
                             procedure is part of a very comprehensive screening procedure (cf. 1.4.2.2)
                             and the only one which also covers most of the synthetic opioids. The anti-
                             tussive pholcodine was found to cross-react with opiate immunoassays, but
                             it lacks opioid potency. Pholcodine is  partly hydrolyzed to morphine by
                             hydrochloric acid, so careful enzymatic hydrolysis must be used if differen-
                             tiation in urine is needed. 198–200  In recent years, buprenorphine and oxyco-
                             done testing became more and more of interest. Since a few years ago,
                             buprenorphine has been used, besides methadone and levomethadol, for
                             heroin substitution therapy as an effective means of decreasing illicit heroin
                             use, crime, HIV risk, and death, and in improving employment and social
                                       201
                             adjustment.  Urine testing can be performed by GC/MS, 83,202,203  while blood
                             testing requires LC/MS, especially for precise quantification. 204–206
                                Oxycodone has very high abuse potential because it is highly effective
                             when taken orally, is often easily available, and has a high degree of consistent
                             potency. Opiate tests might be negative for oxycodone. Therefore, urine
                             specimens must be analyzed specifically for oxycodone, preferably by GC/MS
                             after enzymatic hydrolysis, LLE or SPE, and derivatization by AC, TMS, PFP,
                             or HFB. 1,194,207–210
                                Recently, an improved GC/MS method for the simultaneous identifica-
                                                                               194
                             tion and quantification of opiates in urine was reported.  In this method,
                             methoxyamine was used after enzymatic hydrolysis to form methoxime
                             derivatives of the keto-opiates, which were extracted using solid-phase col-
                             umns and derivatized with propionic anhydride/pyridine. This method dem-
                             onstrated acceptable precision, lack of cross-interference from other opioids,


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