Determination of Sudan I in paprika powder by molecularly imprinted polymers-thin layer chromatography-surface enhanced Raman spectroscopic biosensor

被引:104
作者
Gao, Fang [1 ]
Hu, Yaxi [1 ]
Chen, Da [3 ]
Li-Chan, Eunice C. Y. [1 ]
Grant, Edward [2 ]
Lu, Xiaonan [1 ]
机构
[1] Univ British Columbia, Fac Land & Food Syst, Food Nutr & Hlth Program, Vancouver, BC V6T 1Z4, Canada
[2] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
[3] Tianjin Univ, State Key Lab Precis Measuring Technol & Instrume, Tianjin 300072, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
Molecular imprinting; Raman spectroscopy; Separation; Food safety; Multivariate analysis; GLASSY-CARBON ELECTRODE; MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; SINGLE-MOLECULE; SCATTERING; FOOD; SERS; DYES; QUANTIFICATION; NANOPARTICLES;
D O I
10.1016/j.talanta.2015.05.003
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Sudan I is a carcinogenic and mutagenic azo-compound that has been utilized as a common adulterant in spice and spice blends to impart a desirable red color to foods. A novel biosensor combining molecularly imprinted polymers (MIPs), thin layer chromatography (TLC) and surface enhanced Raman spectroscopy (SERS) could determine Sudan I levels in paprika powder to 1 ppm (or 2 ng/spot). Sudan I spiked paprika extracts (spiking levels: 0, 1, 5, 10, 40, 70 and 100 ppm) were prepared. Sudan I imprinted polymers were synthesized by employing the interaction between Sudan I (template) and methacrylic acid (functional monomer), followed by washing to remove Sudan I leaving the Sudan I-binding sites exposed. MIPs were used as a stationary phase for TLC and could selectively retain Sudan I at the original spot with little interference. A gold colloid SERS substrate could enhance Raman intensity for Sudan I in this MIP-TLC system. Principal component analysis plot and partial least squares regression (R-2=0.978) models were constructed and a linear regression model (R-2=0.983) correlated spiking levels (5, 10, 40, 70 and 100 ppm) with the peak intensities (721 cm(-1)) of Sudan I SERS spectra. Both separation (30-40 s) and detection (1 s or 0.1 s) were extremely fast by using both commercial bench-top and custom made portable Raman spectrometers. This biosensor can be applied as a rapid, low-cost and reliable tool for screening Sudan I adulteration in foods. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:344 / 352
页数:9
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