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Technical Briefs |
1
Department of Clinical Laboratory Sciences, Louisiana State University Health Sciences Center, New Orleans, LA 70112-2262
2
LabOne, Inc., Lenexa, KS 66219-9752
3
LabCorp, Memphis, TN 38118
a author for correspondence: fax 504-568-6761,
lbrous@lsuhsc.edu
Several authors have reviewed existing methods (1)(2)(3)(4)(5)(6)(7)(8)(9) or presented new techniques (6)(7)(8)(9)(10)(11) for the analysis and separation of codeine, morphine, and the keto-opiates hydrocodone, hydromorphone, oxycodone, and oxymorphone. We present a modification of previously published procedures (6)(10) that incorporates the use of methoxyamine after enzymatic hydrolysis to form methoxime derivatives of the keto-opiates, which are then extracted using solid-phase columns and derivatized with propionic anhydride/pyridine.
We used a gas chromatographymass spectrometry system composed of a model 5890 gas chromatograph with splitless injection, a model 5970 mass-selective detector (both from Hewlett Packard), and a DB-5 capillary column [15 m x 0.25 mm (i.d.); 0.25 µm film thickness; J&W Scientific]; helium (flow rate, 0.7 mL/min; linear velocity, 38 cm/s) was used as the carrier gas. The temperature program was as follows: initial temperature, 185 °C; ramp at 25 °C/min to 240 °C; hold for 0.5 min; ramp at 5 °C/min to 250 °C, then 40 °C/min to 290 °C; hold for 1.0 min. The injection temperature was 260 °C, and the transfer line temperature was 290 °C.
The following were obtained from Radian Corporation: (a)
codeine, morphine, hydrocodone, hydromorphone, and oxycodone, which
were used to prepare calibrators; (b) deuterated
codeine, morphine, hydrocodone, and hydromorphone, which were used
as internal standards; and (c) oxymorphone and norcodeine,
which
References
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