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

被引:16
作者
Chen, Guang [1 ,2 ,3 ]
Liu, Jianjun [1 ,2 ]
Liu, Mengge [1 ,2 ]
Li, Guoliang [1 ,2 ]
Sun, Zhiwei [1 ,2 ]
Zhang, Shijuan [3 ]
Song, Cuihua [1 ,2 ]
Wang, Hua [1 ,2 ]
Suo, Yourui [3 ]
You, Jinmao [1 ,2 ,3 ]
机构
[1] Qufu Normal Univ, Key Lab Life Organ Anal, Qufu 273165, Shandong, Peoples R China
[2] Qufu Normal Univ, Key Lab Pharmaceut Intermediates & Anal Nat Med, Qufu 273165, Shandong, Peoples R China
[3] Chinese Acad Sci, Northwest Inst Plateau Biol, Xining 810001, Peoples R China
基金
中国国家自然科学基金;
关键词
Ultrasonic-assisted derivatization; microextraction (UDME); 1-(1H-imidazol-1-yl)-2-(2-phenyl-1H-phenanthro[9,10-d]imidazol-1-yl)ethanone (IPPIE); Aliphatic amines; Environmental samples; UDME-HPLC-FD-MS; SOLID-PHASE MICROEXTRACTION; IONIZATION-MASS-SPECTROMETRY; WATER SAMPLES; GAS-CHROMATOGRAPHY; LABELING REAGENT; PRECOLUMN DERIVATIZATION; ANALYTICAL-CHEMISTRY; BIOGENIC-AMINES; HPLC; PRECONCENTRATION;
D O I
10.1016/j.chroma.2014.05.061
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new fluorescent reagent, 1-(1H-imidazol-1-yl)-2-(2-pheny1-1H-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 (C-1: methylamine-C-12: 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: 43, time: 8 min and temperature: 80 C), micro amount of sample (40 mu L; 5 mg) 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: 0.04-033 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. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 19
页数:12
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