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Determination of fluorescein and brominated fluoresceins in the color additive D&C Orange No. 5 and its lakes using high-performance liquid chromatography.

Authors :
James IC
Lazo-Portugal R
Perez-Gonzalez M
Weisz A
Source :
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment [Food Addit Contam Part A Chem Anal Control Expo Risk Assess] 2019 Dec; Vol. 36 (12), pp. 1800-1807. Date of Electronic Publication: 2019 Sep 19.
Publication Year :
2019

Abstract

The colour additives D&C Orange No. 5 (O5) and its lakes (O5L) are subject to batch certification by the U.S. Food and Drug Administration (FDA) to ensure compliance with specifications in the Code of Federal Regulations (CFR). The present study reports the development of a high-performance liquid chromatography (HPLC) method for the quantitative determination of seven CFR-specified components in O5 and O5L - fluorescein and six brominated fluoresceins. The analytes were quantified using six-point calibration curves with data points (w/w) that ranged as follows: 20.0-70.0% for 4',5'-dibromofluorescein; 9.8-44.1% for 2',4',5'-tribromofluorescein; 1.01-15.2% for 2',4',5',7'-tetrabromofluorescein; 0.10-3.12% for 2',4'-dibromofluorescein; 0.10-3.06% for 2',5'-dibromofluorescein; 0.11-2.85% for 4'-bromofluorescein; and 0.10-2.02% for fluorescein. For all seven analytes, the HPLC instrument response was linear (R <superscript>2</superscript>  > 0.999) over the tested concentration ranges and the limits of detection (0.01-1.55%) were well below the CFR-specified levels. Other validation data showed good analyte recovery (87.91-101.73%) as well as method precision measured by the relative standard deviation (0.53-1.56%). The new method was applied to the analysis of test portions from 15 batches of O5 and eight batches of O5L submitted to FDA for certification by domestic and foreign manufacturers. Compared to the thin-layer chromatography/spectrophotometric procedure currently used for routine batch-certification analyses, the new method was found to be more sensitive, simpler to implement, and significantly faster, requiring 25 minutes rather than six hours to analyse one sample.

Details

Language :
English
ISSN :
1944-0057
Volume :
36
Issue :
12
Database :
MEDLINE
Journal :
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment
Publication Type :
Academic Journal
Accession number :
31535927
Full Text :
https://doi.org/10.1080/19440049.2019.1664773