2006
DOI: 10.1016/j.chroma.2005.11.061
|View full text |Cite
|
Sign up to set email alerts
|

Simultaneous determination of water-soluble and fat-soluble synthetic colorants in foodstuff by high-performance liquid chromatography–diode array detection–electrospray mass spectrometry

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

2
94
2
2

Year Published

2006
2006
2015
2015

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 233 publications
(100 citation statements)
references
References 26 publications
2
94
2
2
Order By: Relevance
“…Comparing with the detection limits reported in literatures [5,7,22,[25][26][27][28], the detection sensitivity was improved more than 10 times (see Table S1, Supporting information).…”
Section: Peakmentioning
confidence: 55%
See 2 more Smart Citations
“…Comparing with the detection limits reported in literatures [5,7,22,[25][26][27][28], the detection sensitivity was improved more than 10 times (see Table S1, Supporting information).…”
Section: Peakmentioning
confidence: 55%
“…Various methods for the determination of dyes in foods have been reported, including capillary electrophoresis [6][7][8][9][10], thinlayer chromatography [11], ion-pair chromatography [12,13], high performance liquid chromatography (HPLC) with ultraviolet/visible (UV/Vis) or diode-array detector (DAD) detection [14][15][16][17][18][19][20][21][22][23][24][25] and liquid chromatography-mass spectrometry (LC-MS) [26][27][28][29][30][31][32]. HPLC coupled with UV/Vis or DAD detection is the most commonly used technique because dyes absorb strongly at the ultraviolet and/or visible wavelength.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Among the components determined using HPLC are carbohydrates (Chávez-Servín et al, 2004;Muir et al, 2009), organic acids (Chinnici et al, 2005Lima et al, 2010), lipids (Puoci et al, 2008), vitamins (Speek et al, 1986;Rodriguez et al, 2012), colorants (Vidotti, et al, 2006;Ma et al, 2006), amino acids and peptides (Zhang et al, 2010;Garai-Ibade et al, 2012), mycotoxins (Kawashima & Soares,maintained at 80 °C and the detector at 50 °C. Sample detection was performed by comparing retention times standards.…”
mentioning
confidence: 99%
“…13 And the effectiveness of the two different extraction solvents on extraction efficiency and analyte recovery were studied with blank samples spiked at a concentration of 0.8 μg/kg for tartrazine, amaranth, carmine, brilliant blue and allura red, and 0.4 μg/kg for sunset yellow and erythrosine. The average recoveries and RSDs of the studied analytes are shown in Fig.…”
Section: Optimization Of Sample Extraction Proceduresmentioning
confidence: 99%