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Fast HPLC Analysis of Dyes in Foods and Beverages

Applications | 2016 | Thermo Fisher ScientificInstrumentation
HPLC
Industries
Food & Agriculture
Manufacturer
Thermo Fisher Scientific

Summary

Importance of the Topic


The use of synthetic colorants in food and beverage products enhances visual appeal, masks imperfections, and reinforces flavor associations. Regulatory authorities restrict permitted dyes to ensure consumer safety. Rapid, accurate detection of both approved and illicit dyes is crucial for effective quality control and public health protection.

Objectives and Study Overview


This work aimed to develop a high-throughput HPLC method capable of separating and quantifying up to ten common food dyes in under five minutes. The method utilizes an Acclaim PA2 column and an UltiMate 3000 RSLC system. Performance was demonstrated through analysis of commercial sports drinks, carbonated beverages, and a gelatin dessert.

Methodology and Instrumentation


Instrumentation:
  • UltiMate 3000 RSLC system: vacuum degasser, binary gradient pump, split-loop sampler, thermostatted column compartment, diode array detector
  • Acclaim PA2 column (3 µm, 3 × 75 mm)
  • Chromeleon Chromatography Data System v6.80 SR7

Chromatographic conditions:
  • Mobile phase A: 20 mM ammonium phosphate buffer, pH 8.8; B: 50% A in acetonitrile
  • Gradient: 12% B to 100% B over 3.5 min, hold 1 min, return to 12% B
  • Flow rate: 0.709 mL/min; column temperature: 30 °C; injection volume: 3 µL
  • Detection: UV absorbance at 254 nm and wavelength scanning (200–800 nm)

A faster configuration employed an Acclaim RSLC PA2 column (2.2 µm, 2.1 × 50 mm), 1 µL injection, 0.5 mL/min flow rate, a 200 µL static mixer and 2.5 µL flow cell to reduce run time to 2.5 min.

Main Results and Discussion


Baseline separation of ten FDA-approved and common dyes was achieved in under five minutes on the PA2 column, with USP resolution values >2.8 and spectral match factors >998. Calibration curves were linear from 1–30 mg/L (r² > 0.999). Analysis of seven commercial samples identified permitted dyes (Tartrazine, Sunset Yellow FCF, Fast Green FCF) and detected the banned dye New Coccine in a gelatin dessert. Recovery studies (82–100%) and five-injection repeatability (RSD < 1% for most analytes) demonstrated method accuracy and precision.

Benefits and Practical Applications


  • High-throughput screening for routine food and beverage quality control
  • Identification of unauthorized dyes to ensure regulatory compliance
  • Compatibility with mass spectrometry for confirmation and expanded analyte coverage

Future Trends and Applications


Advancements in ultra-high-performance LC, smaller particle columns and automated sample preparation are expected to further reduce analysis times and enhance sensitivity. Integration with real-time data processing and portable systems will support on-site food safety monitoring and rapid decision-making.

Conclusion


The presented RSLC method delivers a rapid, robust, and reproducible approach for quantifying and identifying multiple food dyes in complex matrices. Its high pH stability and compatibility with diverse detection methods render it ideal for routine screening and compliance testing.

References


  • Application Note 245: Fast HPLC Analysis of Dyes in Foods and Beverages. Dionex Corporation; 2016.

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