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作 者:孟梁[1] 朱彬玲[1] 郑可芳[1] 张文文 孟品佳[3]
机构地区:[1]福建警察学院刑事科学技术系,福建福州350007 [2]北京市公安局公安交通管理局,北京100037 [3]中国人民公安大学刑事科学技术学院,北京100038
出 处:《色谱》2015年第3期304-308,共5页Chinese Journal of Chromatography
基 金:福建省教育厅中青年教师教育科研项目(JA14336)
摘 要:建立了生物样品中8种毒品的超声辅助分散液液微萃取-气相色谱-三重四极杆串联质谱检测方法,采用密度比水低的有机溶剂甲苯作为萃取溶剂,萃取过程中不需要任何分散剂。对影响萃取富集效率的因素进行优化:将100μL甲苯萃取剂加入到1 mL样品溶液中,超声波剧烈振荡使甲苯充分分散到样品溶液中进行萃取,离心分层后,抽取上层萃取剂供气相色谱-三重四极杆串联质谱分析检测。在优化条件下,分析物在各自的线性范围内具有良好的线性关系,线性相关系数在0.998 4~0.999 4之间;检出限为0.05~0.40μg/L(S/N=3);样品加标回收率在79.3%~100.3%之间,RSD〈5.7%。本方法具有操作简单、灵敏度高和重现性好等优点,可应用于生物样品中多种毒品的分析检测。A novel microextraction technique based on ultrasound-assisted low-density solvent dispersive liquid-liquid microextraction(UA-LDS-DLLME)has been developed for the determination of multiple drugs of abuse in biological samples by gas chromatography-triple quadrupole mass spectrometry(GCQQQ-MS). A total of 100 μL of toluene as extraction solvent was dropped into the sample solution.Then the mixture was sonicated drastically in an ultrasonic bath for 3 min with occasional manual shaking to form a cloudy suspension. After centrifugation at 10 000 r / min for 3 min,the upper layer of lowdensity extractant was withdrawn and injected into the GC-QQQ-MS for analysis. The parameters affecting extraction efficiency have been investigated and optimized. Under the optimum conditions,good linearities were observed for all analytes with the correlation coefficients ranging from 0. 998 4 to 0. 999 4.The recoveries of 79. 3%-100. 3% with RSDs 5. 7% were obtained. The LODs(S / N = 3)were in the range from 0. 05 to 0. 40 μg / L. UA-LDS-DLLME technique has the advantages of less extraction time,suitable for batches of sample pretreatment simultaneously,and higher extraction efficiency. It was successfully applied to the analysis of amphetamines in real human urine samples.
关 键 词:超声 分散液液微萃取 气相色谱-三重四极杆质谱 毒品 生物样品
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