Quantification of methylone and metabolites in rat and human plasma by liquid chromatography-tandem mass spectrometry

被引:8
|
作者
Ellefsen, Kayla N. [1 ,2 ]
Concheiro, Marta [1 ]
Suzuki, Masaki [3 ,4 ]
Rice, Kenner C. [3 ,4 ]
Elmore, Joshua S. [5 ]
Baumann, Michael H. [5 ]
Huestis, Marilyn A. [1 ]
机构
[1] NIDA, Chem & Drug Metab, Intramural Res Program, NIH, Baltimore, MD 21224 USA
[2] Univ Maryland, Toxicol Program, Baltimore, MD 21201 USA
[3] NIDA, Drug Design & Synth Sect, Intramural Res Program, Baltimore, MD 21224 USA
[4] NIAAA, NIH, Baltimore, MD USA
[5] NIDA, Designer Drug Res Unit, Intramural Res Program, NIH, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
Methylone; Synthetic cathinones; Novel designer drugs; Metabolites; 4-Hydroxy-3-methoxymethcathinone; LC-MS/MS; SYNTHETIC CATHINONES; DESIGNER DRUG; BATH SALTS; MEPHEDRONE; MDPV;
D O I
10.1007/s11419-015-0263-z
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Methylone is a commonly abused synthetic cathinone derivative marketed as a "legal" alternative to "ecstasy" or cocaine. Previous studies examined the metabolism of methylone in vitro and in vivo; 4-hydroxy-3-methoxymethcathinone (HMMC) was identified as the primary metabolite, with other reported minor metabolites, 3,4-methylenedioxycathinone (MDC) and 3,4-dihydroxymethcathinone (HHMC). However, limited information is known about methylone and its metabolites' pharmacokinetics. We developed and fully validated a method for the simultaneous quantification of methylone, HMMC, MDC and HHMC by liquid chromatography-tandem mass spectrometry in 100 A mu l rat and human plasma. beta-Glucuronidase was utilized for plasma hydrolysis, followed by perchloric acid protein precipitation and solid-phase extraction utilizing cation exchange columns. Chromatographic separation was performed with a Synergi Polar column in gradient mode, and analytes were determined by two multiple reaction monitoring (MRM) transitions. Linear ranges of 0.5-1,000 A mu g/l (methylone, HMMC and MDC) and 10-1,000 A mu g/l (HHMC) were achieved. Bias and imprecision were generally acceptable, although quantification of HHMC exhibited variability (16.2-37 %). Extraction efficiencies and ion suppression were 89.9-104 % (for HHMC, 15.9-16.2 %) and < 11.4 %, respectively. Methylone and metabolites were stable in plasma for 24 h at room temperature, 72 h at 4 A degrees C, and after three freeze-thaw cycles (except for a 60 % HMMC increase). Human and rat plasma were cross-validated, documenting that rat plasma quality control samples were accurately quantified against a human plasma calibration curve (-23.8 to 12 % bias). As proof of method, rat plasma specimens were analyzed pre-injection and after subcutaneous administration of methylone at 6 mg/kg from 15 to 480 min post-dosing. Methylone, HMMC, MDC and HHMC concentrations ranged from 1.1 to 1,310, 11.2 to 194, 1.9 to 152 and 24.7 to 188 A mu g/l, respectively.
引用
收藏
页码:202 / 212
页数:11
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