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一种快速超声辅助分散液液微萃取结合超高效液相色谱法同时测定人血浆样品中七种苯并二氮杂䓬类药物。

A rapid ultrasound-assisted dispersive liquid-liquid microextraction followed by ultra-performance liquid chromatography for the simultaneous determination of seven benzodiazepines in human plasma samples.

机构信息

Institute of Legal Medicine, Forensic Toxicology Service, Faculty of Medicine, 15782 Santiago de Compostela, Spain.

出版信息

Anal Chim Acta. 2013 Mar 12;767:88-96. doi: 10.1016/j.aca.2013.01.016. Epub 2013 Jan 17.

Abstract

A simple and efficient ultrasound-assisted dispersive liquid-liquid microextraction (UA-DLLME) method has been developed for the determination of seven benzodiazepines (alprazolam, bromazepam, clonazepam, diazepam, lorazepam, lormetazepam and tetrazepam) in human plasma samples. Chloroform and methanol were used as extractant and disperser solvents, respectively. The influence of several variables (e.g., type and volume of dispersant and extraction solvents, pH, ultrasonic time and ionic strength) was carefully evaluated and optimized, using an asymmetric screening design 3(2)4(2)//16. Analysis of extracts was performed by ultra-performance liquid chromatography coupled with photodiode array detection (UPLC-PDA). Under the optimum conditions, two reversed-phases, Shield RP18 and C18 columns were successfully tested, obtaining good linearity in a range of 0.01-5μgmL(-1), with correlation coefficients r>0.996. Quantification limits ranged between 4.3-13.2ngmL(-1) and 4.0-14.8ngmL(-1), were obtained for C18 and Shield RP18 columns, respectively. The optimized method exhibited a good precision level, with relative standard deviation values lower than 8%. The recoveries studied at two spiked levels, ranged from 71 to 102% for all considered compounds. The proposed method was successfully applied to the analysis of seven benzodiazepines in real human plasma samples.

摘要

建立了一种简单高效的超声辅助分散液液微萃取(UA-DLLME)方法,用于测定人血浆样品中的七种苯并二氮䓬类药物(阿普唑仑、溴马唑仑、氯硝西泮、地西泮、劳拉西泮、氯美扎酮和佐匹克隆)。氯仿和甲醇分别用作萃取剂和分散剂溶剂。使用非对称筛选设计 3(2)4(2)//16 仔细评估和优化了几种变量(例如,分散剂和萃取溶剂的类型和体积、pH、超声时间和离子强度)。采用超高效液相色谱-光电二极管阵列检测(UPLC-PDA)对提取物进行分析。在最佳条件下,成功测试了两种反相 Shield RP18 和 C18 柱,在 0.01-5μgmL(-1)范围内获得了良好的线性,相关系数 r>0.996。Shield RP18 和 C18 柱的定量限分别为 4.3-13.2ngmL(-1)和 4.0-14.8ngmL(-1)。优化后的方法表现出良好的精密度水平,相对标准偏差值低于 8%。在两个加标水平下研究的回收率,所有考虑的化合物均在 71%至 102%之间。该方法成功应用于真实人血浆样品中七种苯并二氮䓬类药物的分析。

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