科研之友
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摘要
Levamisole is an anti-helminthic drug and gained forensic interest after it was found that it was used as a cocaine adulterant. A liquid chromatography-mass spectrometry (LC-MS) method for the determination of levamisole and its metabolite aminorex in human plasma is described. Selectivity is given; calibration curves were linear within a calibration range of 1ng/mL-500ng/mL. Limits of detection and quantification (LODs, LOQs) were 0.85ng/mL for levamisole and 0.09ng/mL, and 0.34ng/mL for aminorex, respectively. Precision data was in accordance with the GTFCh guidelines. The validated method was successfully applied to study the pharmacokinetics of levamisole after administration of 100mg of levamisole orally. Levamisole could be detected up to 36h after ingestion in serum, while aminorex never exceeded the LOQ. A one-compartment model best described levamisole pharmacokinetics. The following parameters were calculated: ka=1.2 [1/h], CL/F=52l/h, V/F=347l, f (renal)=0.0005, t 1/2=2.0h, AUC=1923ng/mL*h, cmax=214ng/mL, tmax=1.98h. Levamisole could be quantified in 42.5% of cocaine - positive plasma samples (2.2 to 224ng/mL). Aminorex was positive in only 11.3% of the cases; however, it was never found higher than the LOQ. Pemoline, another stimulant detected in horse urine samples after administration of levamisole, was not found either in serum or in urine of this pharmacokinetic study. In post-mortem cases, levamisole and aminorex could be detected in femoral blood and the urine of cocaine users. Pemoline was not detected.
- 出版日期2014-10
