检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:杨思瑶 何洪源[1] 蒋力维 吕建霞 滕傲雪 YANG Si-yao;HE Hong-yuan;JIANG Li-wei;LÜJian-xia;TENG Ao-xue(School of Criminal Investigation,People’s Public Security University of China,Beijing 100038,China;National Narcotics Laboratory Beijing Regional Center,Beijing 100164,China;Criminal Crime Investigation Bureau of Chengdu Public Security Bureau,Chengdu 610000,China)
机构地区:[1]中国人民公安大学侦查学院,北京100038 [2]国家毒品实验室北京分中心,北京100164 [3]成都市公安局刑事犯罪侦查局,四川成都610000
出 处:《分析测试学报》2025年第4期583-592,共10页Journal of Instrumental Analysis
基 金:中国人民公安大学刑事科学技术双一流创新研究专项(2023SYL06);北京市科技计划资助项目(Z221100005222006)。
摘 要:建立了液相色谱-串联质谱(LC-MS/MS)对尿液和血液中8种合成大麻素及7种代谢物进行定性和定量分析的方法。尿液、血液样品经甲醇-乙腈(体积比1∶1)混合溶液提取后,高速离心取上清液,以0.1%甲酸水溶液和乙腈作为流动相进行梯度洗脱,采用C18色谱柱进行分离,电喷雾电离源(ESI+)多反应监测模式(MRM)进行检测,可在15 min内完成15种目标物的分析。结果显示,尿液中15种目标物在1~200 ng/mL范围内线性关系良好,检出限为0.01~0.10 ng/mL,定量下限为0.03~0.34 ng/mL;血液中15种目标物在0.50~200 ng/mL范围内线性关系良好,检出限为0.01~0.20 ng/mL,定量下限为0.03~0.66 ng/mL。3个不同加标浓度下,15种目标物在尿液、血液中的提取回收率分别为92.2%~105%和82.2%~117%。该方法灵敏度高、分离效果好、操作简便,适用于尿液和血液中多种合成大麻素类物质的定性定量分析。A liquid chromatography-tandem mass spectrometry(LC-MS/MS)method was developed for the qualitative and quantitative analysis of eight synthetic cannabinoids and seven metabolites in urine and blood.After the urine and blood samples were extracted by a mixture of methanol-acetonitrile(1∶1,volume ratio),the supernatant was extracted by high-speed centrifugation,and the gradient elution was carried out with an aqueous solution containing 0.1%formic acid and acetonitrile as the mobile phase,and the separation was carried out on a C18 chromatography column.The ion source for the tandem mass spectrometry was an electrospray ionization source(ESI+),and the detection was performed in multiple reaction monitoring(MRM)mode.The method can be used for the analysis of 15 targets within 15 min.The results showed that the 15 targets exhibited a good linear relationship in the range of 1-200 ng/mL in urine,the limits of detection(LODs)were 0.01-0.10 ng/mL,and the limits of quantification(LOQs)were 0.03-0.34 ng/mL.The 15 targets exhibited a good linear relationship in the range of 0.50-200 ng/mL in blood,LODs were 0.01-0.20 ng/mL,and LOQs were 0.03-0.66 ng/mL.The recoveries in urine and blood at three different spiked concentrations were 92.2%-105%and 82.2%-117%.The developed method is sensitive,effective in separation,easy to operate,and suitable for the determination analysis of synthetic cannabinoid analogs in urine and blood.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.7