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采用超声辅助衍生化微萃取-新荧光试剂高效液相色谱法灵敏、准确、快速检测环境样品中痕量脂肪胺。

Sensitive, accurate and rapid detection of trace aliphatic amines in environmental samples with ultrasonic-assisted derivatization microextraction using a new fluorescent reagent for high performance liquid chromatography.

机构信息

The Key Laboratory of Life-Organic Analysis, Qufu Normal University, Qufu 273165, Shandong, China; Key Laboratory of Pharmaceutical Intermediates and Analysis of Natural Medicine, Qufu Normal University, Qufu 273165, Shandong, China; Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining 810001, China.

The Key Laboratory of Life-Organic Analysis, Qufu Normal University, Qufu 273165, Shandong, China; Key Laboratory of Pharmaceutical Intermediates and Analysis of Natural Medicine, Qufu Normal University, Qufu 273165, Shandong, China.

出版信息

J Chromatogr A. 2014 Jul 25;1352:8-19. doi: 10.1016/j.chroma.2014.05.061. Epub 2014 Jun 2.

Abstract

A new fluorescent reagent, 1-(1H-imidazol-1-yl)-2-(2-phenyl-1H-phenanthro[9,10-d]imidazol-1-yl)ethanone (IPPIE), is synthesized, and a simple pretreatment based on ultrasonic-assisted derivatization microextraction (UDME) with IPPIE is proposed for the selective derivatization of 12 aliphatic amines (C1: methylamine-C12: dodecylamine) in complex matrix samples (irrigation water, river water, waste water, cultivated soil, riverbank soil and riverbed soil). Under the optimal experimental conditions (solvent: ACN-HCl, catalyst: none, molar ratio: 4.3, time: 8 min and temperature: 80°C), micro amount of sample (40 μL; 5mg) can be pretreated in only 10 min, with no preconcentration, evaporation or other additional manual operations required. The interfering substances (aromatic amines, aliphatic alcohols and phenols) get the derivatization yields of <5%, causing insignificant matrix effects (<4%). IPPIE-analyte derivatives are separated by high performance liquid chromatography (HPLC) and quantified by fluorescence detection (FD). The very low instrumental detection limits (IDL: 0.66-4.02 ng/L) and method detection limits (MDL: 0.04-0.33 ng/g; 5.96-45.61 ng/L) are achieved. Analytes are further identified from adjacent peaks by on-line ion trap mass spectrometry (MS), thereby avoiding additional operations for impurities. With this UDME-HPLC-FD-MS method, the accuracy (-0.73-2.12%), precision (intra-day: 0.87-3.39%; inter-day: 0.16-4.12%), recovery (97.01-104.10%) and sensitivity were significantly improved. Successful applications in environmental samples demonstrate the superiority of this method in the sensitive, accurate and rapid determination of trace aliphatic amines in micro amount of complex samples.

摘要

一种新的荧光试剂,1-(1H-咪唑-1-基)-2-(2-苯基-1H-菲咯[9,10-d]咪唑-1-基)乙酮(IPPIE)被合成,并且提出了一种基于超声辅助衍生化微萃取(UDME)的简单预处理方法,用于选择性衍生化复杂基质样品(灌溉水、河水、废水、栽培土、河岸土和河床土)中的 12 种脂肪胺(C1:甲胺-C12:十二胺)。在最佳实验条件下(溶剂:ACN-HCl,催化剂:无,摩尔比:4.3,时间:8 分钟,温度:80°C),仅需 10 分钟即可预处理微摩尔量的样品(40 μL;5mg),无需预浓缩、蒸发或其他额外的手动操作。干扰物质(芳香胺、脂肪醇和酚类)的衍生化产率<5%,不会产生明显的基质效应(<4%)。IPPIE-分析物衍生物通过高效液相色谱(HPLC)分离,并通过荧光检测(FD)定量。仪器检测限(IDL:0.66-4.02ng/L)和方法检测限(MDL:0.04-0.33ng/g;5.96-45.61ng/L)非常低。通过在线离子阱质谱(MS)从相邻峰中进一步鉴定分析物,从而避免了杂质的额外操作。使用这种 UDME-HPLC-FD-MS 方法,提高了准确性(-0.73-2.12%)、精密度(日内:0.87-3.39%;日间:0.16-4.12%)、回收率(97.01-104.10%)和灵敏度。在环境样品中的成功应用证明了该方法在微摩尔量复杂样品中痕量脂肪胺的灵敏、准确和快速测定中的优越性。

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