Coupling carbon nanotube film microextraction with desorption corona beam ionization for rapid analysis of Sudan dyes (I–IV) and Rhodamine B in chilli oil
| Autor: | Xiao-Mei He, Zhi-Guo Shi, Di Chen, Yun-Qing Huang, Yu-Qi Feng |
|---|---|
| Rok vydání: | 2015 |
| Předmět: |
Detection limit
Chromatography Nanotubes Carbon Selected reaction monitoring Extraction (chemistry) Analytical chemistry Biochemistry Ion source Analytical Chemistry chemistry.chemical_compound chemistry Linear range Spectrometry Mass Matrix-Assisted Laser Desorption-Ionization Desorption Ionization Electrochemistry Rhodamine B Plant Oils Environmental Chemistry Food Additives Capsicum Coloring Agents Azo Compounds Solid Phase Microextraction Spectroscopy |
| Zdroj: | The Analyst. 140:1731-1738 |
| ISSN: | 1364-5528 0003-2654 |
| DOI: | 10.1039/c4an02044h |
| Popis: | A rapid analysis method by coupling carbon nanotube film (CNTF) microextraction with desorption corona beam ionization (DCBI) was developed for the determination of Sudan dyes (I-IV) and Rhodamine B in chilli oil samples. Typically, CNTF was immersed into the diluted solution of chilli oil for extraction, which was then placed directly under the visible plasma beam tip of the DCBI source for desorption and ionization. Under optimized conditions, five dyes were simultaneously determined using this method. Results showed that the analytes were enriched by the CNTF through the π-π interactions, and the proposed method could significantly improve the sensitivities of these compounds, compared to the direct analysis by DCBI-MS/MS. The method with a linear range of 0.08-12.8 μg g(-1) and good linear relationships (R(2)0.93) in a multiple reaction monitoring (MRM) mode was developed. Satisfactory reproducibility was achieved. Relative standard deviations (RSDs) were less than 20.0%. The recoveries ranged from 80.0 to 110.0%, and the limits of detection (LODs) were in the range of 1.4-21 ng g(-1). Finally, the feasibility of the method was further exhibited by the determination of five illegal dyes in chilli powder. These results demonstrate that the proposed method consumes less time and solvent than conventional HPLC-based methods and avoids the contamination of chromatographic column and ion source from non-volatile oil. With the help of a 72-well shaker, multiple samples could be treated simultaneously, which ensures high throughput for the entire pretreatment process. In conclusion, it provides a rapid and high-throughput approach for the determination of such illicit additions in chilli products. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|