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棒状吸附微萃取中粉末活性炭的研制用于分析人尿中的吗啡和可待因。

Development of a powdered activated carbon in bar adsorptive micro-extraction for the analysis of morphine and codeine in human urine.

作者信息

Gonçalves A F P, Neng N R, Mestre A S, Carvalho A P, Nogueira J M F

机构信息

University of Lisbon, Faculty of Sciences, Chemistry and Biochemistry Department and Centre of Chemistry and Biochemistry, Campo Grande Ed. C8, 1749-016 Lisbon, Portugal.

出版信息

J Chromatogr Sci. 2012 Aug;50(7):574-81. doi: 10.1093/chromsci/bms051. Epub 2012 May 3.

DOI:10.1093/chromsci/bms051
PMID:22562817
Abstract

In the present work, bar adsorptive microextraction using an activated carbon (AC) adsorbent phase followed by liquid desorption and high-performance liquid chromatography with diode array detection was developed to monitor morphine (MOR) and codeine (COD) in human urine. Under optimized experimental conditions, assays performed in aqueous media spiked at the 30.0 µg/L level yielded recoveries of 41.3 ± 1.3% for MOR and 38.4 ± 1.7% for COD, respectively. The textural and surface chemistry properties of the AC phase were also correlated with the analytical data for a better understanding of the overall enrichment process. The analytical performance showed good precision (relative standard deviation < 8.0%), suitable detection limits (0.90 and 0.06 µg/L for MOR and COD, respectively) and convenient linear dynamic ranges (r(2) > 0.991) from 10.0 to 330.0 µg/L. By using the standard addition methodology, the applications of this analytical approach to water and urine matrices allowed remarkable performance to monitor MOR and COD at the trace level. This new confirmatory method proved to be a suitable alternative to other sorptive micro-extraction methodologies in monitoring trace levels of opiate-related compounds, because it was easy to implement, reliable, sensitive and required a low sample volume.

摘要

在本研究中,开发了一种采用活性炭(AC)吸附相的棒式吸附微萃取方法,随后进行液体解吸,并结合二极管阵列检测的高效液相色谱法,用于监测人尿中的吗啡(MOR)和可待因(COD)。在优化的实验条件下,对加标浓度为30.0 µg/L的水性介质进行分析,MOR和COD的回收率分别为41.3±1.3%和38.4±1.7%。还将AC相的结构和表面化学性质与分析数据相关联,以更好地理解整个富集过程。分析性能显示出良好的精密度(相对标准偏差<8.0%)、合适的检测限(MOR和COD分别为0.90和0.06 µg/L)以及10.0至330.0 µg/L的便捷线性动态范围(r(2)>0.991)。通过使用标准加入法,该分析方法在水和尿液基质中的应用能够以卓越的性能监测痕量水平的MOR和COD。这种新的确证方法被证明是监测痕量阿片类相关化合物时其他吸附微萃取方法的合适替代方法,因为它易于实施、可靠、灵敏且所需样品体积小。

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