Simultaneous LC-MS/MS determination of JWH-210, RCS-4, Δ9-tetrahydrocannabinol, and their main metabolites in pig and human serum, whole blood, and urine for comparing pharmacokinetic data

被引:25
|
作者
Schaefer, Nadine [1 ]
Kettner, Mattias [1 ]
Laschke, Matthias W. [2 ]
Schlote, Julia [1 ]
Peters, Benjamin [1 ]
Bregel, Dietmar [1 ]
Menger, Michael D. [2 ]
Maurer, Hans H. [3 ]
Ewald, Andreas H. [1 ]
Schmidt, Peter H. [1 ]
机构
[1] Univ Saarland, Inst Legal Med, D-66421 Homburg, Saar, Germany
[2] Univ Saarland, Inst Clin & Expt Surg, D-66421 Homburg, Saar, Germany
[3] Univ Saarland, Dept Expt & Clin Toxicol, D-66421 Homburg, Saar, Germany
关键词
Synthetic cannabinoids; Tetrahydrocannabinol; Validation; Pigs; LC-MS/MS; Pharmacokinetics; TANDEM MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION; SYNTHETIC CANNABINOIDS; GAS-CHROMATOGRAPHY; THC-COOH; DESIGNER DRUGS; QUANTIFICATION; VALIDATION; SAMPLES; INTOXICATION;
D O I
10.1007/s00216-015-8605-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A series of new synthetic cannabinoids (SC) has been consumed without any toxicological testing. For example, pharmacokinetic data have to be collected from forensic toxicological case work and/or animal studies. To develop a corresponding model for assessing such data, samples of controlled pig studies with two selected SC (JWH-210, RCS-4) and, as reference, a dagger(9)-tetrahydrocannabinol (THC) should be analyzed as well as those of human cases. Therefore, a method for determination of JWH-210, RCS-4, THC, and their main metabolites in pig and human serum, whole blood, and urine samples is presented. Specimens were analyzed by liquid-chromatography tandem mass spectrometry and multiple-reaction monitoring with three transitions per compound. Full validation was carried out for the pig specimens and cross-validation for the human specimens concerning precision and bias. For the pig studies, the limits of detection were between 0.05 and 0.50 ng/mL in serum and whole blood and between 0.05 and 1.0 ng/mL in urine, the lower limits of quantification between 0.25 and 1.0 ng/mL in serum and 0.50 and 2.0 ng/mL in whole blood and urine, and the intra- and interday precision values lower than 15 % and bias values within +/- 15 %. The applicability was tested with samples taken from a pharmacokinetic pilot study with pigs following intravenous administration of a mixture of 200 mu g/kg body mass dose each of JWH-210, RCS-4, and THC. The cross-validation data for human serum, whole blood, and urine showed that this approach should also be suitable for human specimens, e.g., of clinical or forensic cases.
引用
收藏
页码:3775 / 3786
页数:12
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