Choi Yun Jeong, Sim Arum, Kim Min Kyung, Suh Sunglll, In Moon Kyo, Kim Jin Young
Forensic Science Division II, Supreme Prosecutors' Office, Seoul 06590, Republic of Korea.
Office of Forensic Science Planning, Supreme Prosecutors' Office, Seoul 06590, Republic of Korea.
J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Sep 1;1029-1030:22-27. doi: 10.1016/j.jchromb.2016.06.045. Epub 2016 Jun 27.
Nonmedical use of prescription stimulants such as phentermine (PT) has been regulated by law enforcement authorities due to its euphorigenic and relaxing effects. Due to high potential for its abuse, reliable analytical methods were required to detect and identify PT and its metabolite in biological samples. Thus a dilute and shoot liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for simultaneous determination of PT, N-hydroxyphentermine (NHOPT) and mephentermine (MPT) in urine. A 5μL aliquot of diluted urine was injected into the LC-MS/MS system. Chromatographic separation was performed by reversed-phase C18 column with gradient elution for all analytes within 5min. Identification and quantification were based on multiple reaction monitoring (MRM) detection. Linear least-squares regression with a 1/x(2) weighting factor was used to generate a calibration curve and the assay was linear from 50 to 15000ng/mL (PT and MPT) and 5 to 750ng/mL (NHOPT). The intra- and inter-day precisions were within 8.9% while the intra- and inter-day accuracies ranged from -6.2% to 11.2%. The limits of quantification were 3.5ng/mL (PT), 1.5ng/mL (NHOPT) and 1.0ng/mL (MPT). Method validation requirements for selectivity, dilution integrity, matrix effect and stability were satisfied. The applicability of the developed method was examined by analyzing urine samples from drug abusers.
由于其具有致欣快和放松作用,苯丁胺(PT)等处方兴奋剂的非医疗用途已受到执法当局的监管。由于其滥用潜力高,需要可靠的分析方法来检测和鉴定生物样品中的PT及其代谢物。因此,开发并验证了一种稀释进样液相色谱 - 串联质谱(LC-MS/MS)方法,用于同时测定尿液中的PT、N-羟基苯丁胺(NHOPT)和甲苯丁胺(MPT)。将5μL稀释尿液等分试样注入LC-MS/MS系统。通过反相C18柱进行色谱分离,所有分析物在5分钟内梯度洗脱。基于多反应监测(MRM)检测进行鉴定和定量。采用具有1/x(2)加权因子的线性最小二乘回归生成校准曲线,该方法在50至15000ng/mL(PT和MPT)以及5至750ng/mL(NHOPT)范围内呈线性。日内和日间精密度在8.9%以内,日内和日间准确度在-6.2%至11.2%之间。定量限分别为3.5ng/mL(PT)、1.5ng/mL(NHOPT)和1.0ng/mL(MPT)。满足了选择性、稀释完整性、基质效应和稳定性的方法验证要求。通过分析吸毒者的尿液样本检验了所开发方法的适用性。