...
首页> 外文期刊>Journal of Analytical Toxicology >Rapid Separation and Quantitation of Cocaine and its Metabolites in Human Serum by Differential Mobility Spectrometry–tandem Mass Spectrometry (DMS–MS-MS)
【24h】

Rapid Separation and Quantitation of Cocaine and its Metabolites in Human Serum by Differential Mobility Spectrometry–tandem Mass Spectrometry (DMS–MS-MS)

机译:通过差分迁移光谱法质谱(DMS-MS-MS)快速分离和定量人血清中的人血清中的代谢产物

获取原文
获取原文并翻译 | 示例

摘要

Cocaine continues to be one of the most widespread abused illicit drugs in the USA. Rapid methods are needed for the identification and quantitation of cocaine and its metabolites, benzoylecgonine (BE), ecgonine methyl ester (EME) and cocaethylene (CE), in biological specimens by clinical and forensic toxicology laboratories. Presented is a differential ion mobility spectrometry–tandem mass spectrometry (DMS–MS-MS) method for the analysis of cocaine and its major metabolites in human serum that requires minimal sample preparation and no column chromatography. A Shimadzu Nexera X2 ultra-high performance liquid chromatography system was used to infuse the samples into the DMS cell at a rate of 30 μL/min. Separation of cocaine and its metabolites were performed in a SelexION DMS component from Sciex coupled to a QTRAP 6500 with an IonDrive Turbo V source for TurbolonSpray? using acetonitrile as a chemical modifier. Analysis consisted of ramping the CoV from ?35 V to ?6 V while monitoring the multiple reaction monitoring (MRM) transitions of each analyte. The assay was evaluated for linearity, bias, precision, carryover, interferences and stability. Calibration curves ranged from 10 to 1,000 ng/mL with linear regression correlation coefficients (r2) of 0.9912 or greater for each analyte. The limit of quantitation was set at 10 ng/mL. Intra-day precision (%CV) ranged from 0% to 15% for cocaine, 1% to 19% for BE, 1% to 17% for EME and 0% to 18% for CE. Inter-day precision ranged from 9% to 14% for cocaine, 2% to 17% for BE, 5% to 11% for EME and 5% to 15% for CE. No carryover or interferences were detected. Bland–Altman analysis of previously analyzed specimens by UPLC–MS-MS showed variability of 30% or less. The method demonstrates the applicability of DMS–MS-MS for high throughout analysis of drugs and their metabolites in clinical and forensic toxicology laboratories.
机译:可卡因仍然是美国最普遍滥用的非法毒品之一。通过临床和法医学毒理学实验室,在生物标本中鉴定和定量可卡因及其代谢物,苯甲酰葡萄球菌(EME)和环丁基(CE)所需的快速方法。呈现是差分离子迁移光谱法 - 串联质谱(DMS-MS-MS)方法,用于分析可卡因及其在人血清中的主要代谢物,需要最小的样品制备和无柱色谱。 Shimadzu Nexera X2超高效液相色谱系统用于以30μl/ min的速率将样品注入DMS电池。可卡因和其代谢物的分离在来自SCIEx的SELEXION DMS组件中进行,与Turbolonspray的离子涡轮v源相耦合到Qtrap 6500?使用乙腈作为化学改性剂。分析包括将COV从15 V升至6 V,同时监测每个分析物的多次反应监测(MRM)转换。评估测定的线性,偏差,精度,携带,干扰和稳定性。校准曲线范围为10至1,000ng / ml,每个分析物为0.9912或更大的线性回归相关系数(R2)。定量限设定为10ng / ml。可卡因的日期精度(%CV)的含量为0%至15%,1%〜19%,EME的1%至17%,CE为0%至18%。当天间精度范围为可卡因的9%至14%,EME的2%至17%,5%至11%,CE的5%至15%。没有检测到残留或干扰。通过UPLC-MS-MS对先前分析的标本的平坦-Altman分析显示为30%或更低的可变性。该方法证明了DMS-MS-MS在临床和法医学毒理学实验室中的药物和代谢物的高度分析的适用性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号