Laboratory of Pharmacology-Toxicology, Raymond Poincaré University Hospital, Versailles Saint Quentin-en-Yvelines University, 104 Boulevard Raymond Poincaré, 92380 Garches, France.
Anal Bioanal Chem. 2013 Jan;405(1):239-45. doi: 10.1007/s00216-012-6470-0. Epub 2012 Oct 19.
Methoxetamine is a new ketamine derivative designer drug which has recently become available via the Internet marketed as "legal ketamine". It is a new dissociative recreational drug, acting as an NMDA receptor antagonist and dopamine reuptake inhibitor. The objective of this study was to develop on-line automated sample preparation using a TurboFlow device coupled with liquid chromatography with ion-trap mass spectrometric detection for measurement of methoxetamine in human plasma. Samples (100 μL) were vortex mixed with internal standard solution (ketamine-d4 in acetonitrile). After centrifugation, 20 μL of the supernatant was injected on to a 50 mm × 0.5-mm C18XL Turboflow column. The retained analytes were then back-flushed on to a 50 mm × 3-mm (3 μm) Hypersil Gold analytical column for chromatographic separation, then eluted with a formate buffer-acetonitrile gradient. Methoxetamine and the IS were ionized by electrospray in positive mode. Parent M + H ions were m/z 248.1 for methoxetamine and m/z 242.0 for the IS. The most intense product ions from methoxetamine (m/z 203.0) and the IS (m/z 224.0) were used for quantification. The assay was accurate (96.8-108.8% range) and precise (intra and inter-day coefficients of variation <8.8%) over the range of 2.0 (lower limit of quantification) to 1000.0 ng mL(-1) (upper limit of quantification). No matrix effect was observed. This method has been successfully applied to determination of plasma concentrations of methoxetamine in the first French hospitalization case report after acute intoxication; the plasma concentration was 136 ng mL(-1).
甲氧基凯他命是一种新型的氯胺酮类合成毒品,最近通过互联网以“合法氯胺酮”的名义出售。它是一种新型的分离性娱乐性药物,作为 NMDA 受体拮抗剂和多巴胺再摄取抑制剂。本研究的目的是开发在线自动样品制备,使用 TurboFlow 装置与液相色谱-离子阱质谱联用,用于测量人血浆中的甲氧基凯他命。样品(100 μL)与内标溶液(氯胺酮-d4 在乙腈中)涡旋混合。离心后,取 20 μL 上清液注入 50mm×0.5mm C18XL TurboFlow 柱。保留的分析物然后反向冲洗到 50mm×3mm(3μm)Hypersil Gold 分析柱进行色谱分离,然后用甲酸缓冲液-乙腈梯度洗脱。甲氧基凯他命和内标通过正电喷雾电离。母体[M+H]+离子为甲氧基凯他命 m/z 248.1,内标 m/z 242.0。从甲氧基凯他命(m/z 203.0)和内标(m/z 224.0)中获得最强的产物离子用于定量。该测定法在 2.0(定量下限)至 1000.0ng·mL-1(定量上限)范围内具有准确性(96.8-108.8%)和精密度(日内和日间变异系数<8.8%)。未观察到基质效应。该方法已成功应用于首例法国急性中毒住院病例报告中测定血浆中甲氧基凯他命浓度;血浆浓度为 136ng·mL-1。