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Analysis of Melamine and Cyanuric Acid Using a Core Enhanced Technology Accucore HILIC HPLC column

Applications | 2011 | Thermo Fisher ScientificInstrumentation
Consumables, LC columns, LC/SQ
Industries
Food & Agriculture
Manufacturer
Thermo Fisher Scientific

Summary

Significance of the Topic

Rapid and high-throughput analysis of polar contaminants such as melamine and its degradation product cyanuric acid is critical for food safety. Incidents of melamine adulteration in dairy products have led to stringent regulations requiring sensitive, reliable detection methods. Hydrophilic interaction liquid chromatography (HILIC) coupled with mass spectrometry offers a robust solution for such analyses.

Objectives and Study Overview

The purpose of this study is to evaluate a core enhanced Accucore HILIC HPLC column for fast separation of melamine and cyanuric acid at conventional backpressures, demonstrating its applicability for routine quality control and regulatory compliance.

Methodology and Instrumentation

Sample Preparation:
Standard solutions of melamine and cyanuric acid (3 mg/mL each in DMSO) were diluted with DMSO:mobile phase (1:3) to 70 μg/mL.

Chromatographic Conditions:
  • Column: Accucore HILIC 2.6 μm, 150 x 4.6 mm
  • Mobile phase: 90:10 acetonitrile:50 mM ammonium acetate, pH 5
  • Flow rate: 1.0 mL/min, Column temperature: 40 °C
  • Injection volume: 5 μL
Mass Spectrometry:
  • System: Thermo Scientific Accela HPLC with MS detection
  • Detection modes: negative (0–3 min), positive (3–10 min)
  • Transitions: cyanuric acid m/z 128.1 [M–H]–; melamine m/z 127.1 [M+H]+, 168.1 [M+41+H]+
Instrumentation Used:
  • Thermo Scientific Accucore HILIC column (17526-154630)
  • Thermo Scientific Accela HPLC system
  • LC-MS grade solvents and reagents

Main Results and Discussion

Melamine and cyanuric acid were baseline separated in under 5 minutes (cyanuric acid at 2.15 min, melamine at 4.61 min) with backpressure around 117 bar. Precision was excellent, with retention time RSDs of 0.4% and 0.3% for cyanuric acid and melamine, respectively. The core-shell particle technology allowed high efficiency and low pressure, facilitating rapid analysis without sacrificing resolution.

Benefits and Practical Applications

  • Fast throughput: separation completed in less than 5 minutes
  • Compatibility: operates at typical HPLC pressures (<120 bar)
  • Suitability: ideal for routine screening in food safety laboratories

Future Trends and Application Possibilities

Expanding this HILIC methodology to other polar contaminants and metabolites can enhance laboratory efficiency. Combining core-shell columns with advanced MS detectors and automated sample preparation may further increase throughput. Online coupling with sample clean-up techniques could support real-time monitoring in quality control settings.

Conclusion

The Accucore HILIC column demonstrates rapid, robust, and precise analysis of melamine and cyanuric acid, meeting regulatory requirements while maintaining standard HPLC conditions. This approach enhances analytical workflows in food safety labs.

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