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Simultaneous Extraction of Melamine and Cyanuric Acid from Food Products Using Strata® Melamine SPE and Ultra-fast LC/MS/MS Analysis Using Kinetex™ HILIC, Rapid LC/MS/MS Analysis on Luna® HILIC, or Rapid GC/MS Analysis on Zebron™ ZB-XLB HT

Applications | 2009 | PhenomenexInstrumentation
GC/MSD, Sample Preparation, GC columns, Consumables, LC/MS, LC/MS/MS, LC columns, LC/QQQ
Industries
Food & Agriculture
Manufacturer
Agilent Technologies, Phenomenex, SCIEX

Summary

Significance of the topic


The contamination of food products with melamine and cyanuric acid poses serious health risks, including kidney failure, and has prompted stringent regulatory scrutiny worldwide. Their high water solubility and propensity to form poorly soluble complexes require robust analytical methods for reliable detection at trace levels.

Objectives and study overview


This study aimed to develop a streamlined workflow for simultaneous extraction and quantitation of melamine and cyanuric acid in food matrices. Key goals included:
  • Combining extraction steps into a single procedure using Strata Melamine SPE cartridges.
  • Establishing ultra-fast chromatographic methods via LC/MS/MS and a rapid GC/MS approach.
  • Validating performance in baby formula and extending to tissue matrices.

Methodology


Sample preparation involved spiking baby formula with analytes and isotopic internal standards, followed by protein precipitation with acetonitrile and acidification. The supernatant was processed on 200 mg/3 mL Strata Melamine SPE cartridges under controlled conditioning, loading, wash, and elution steps. Eluates were evaporated, reconstituted in mobile phase, and divided for LC/MS/MS and GC/MS analysis. Chromatographic conditions included:
  • LC/MS/MS on Kinetex HILIC (50×2.1 mm) for sub-minute separation and on Luna HILIC (100×2.0 mm) for complete analysis under 3 minutes. MS operated in MRM mode with polarity switching.
  • GC/MS on a Zebron ZB-XLB-HT Inferno column (15 m×0.25 mm×0.25 µm) with derivatization, achieving baseline separation in under 9 minutes.

Used instrumentation


  • Strata Melamine SPE cartridges (Phenomenex)
  • Agilent 1100 series HPLC with on-line degasser and column heater
  • API3000 tandem mass spectrometer with TurboIonSpray source
  • Kinetex core-shell HILIC columns
  • Luna HILIC columns
  • GC system equipped with Zebron ZB-XLB-HT Inferno column

Main results and discussion


The combined SPE/protein precipitation workflow yielded absolute recoveries of 67 % for melamine and 68 % for cyanuric acid, with relative recoveries of 67 % and 94.5 %, respectively, and coefficients of variation below 5 %. Calibration curves over 20–2000 ng/g displayed excellent linearity (R² > 0.999). The LLOQ was 200 ng/g (CV < 20 %), and the LOD reached 20 ng/g. Rapid LC/MS/MS analyses achieved full separation in under 0.4 minutes on Kinetex and under 3 minutes on Luna. Similarly, GC/MS provided complete resolution within 9 minutes. The method was readily adapted to tissue matrices using an FDA bulletin-based homogenization and cleanup procedure.

Benefits and practical applications


This integrated approach reduces sample handling and analysis time, allowing high-throughput screening of food and biological samples. The method comfortably meets the WHO limit of 1 mg/kg for both analytes and is compatible with existing LC/MS/MS and GC/MS laboratory setups.

Future trends and potential applications


Advances in core-shell stationary phases and ultra-high-pressure LC promise even faster separations. Further miniaturization of SPE formats and coupling with high-resolution mass spectrometry will enhance sensitivity and selectivity. The workflow could be extended to other polar contaminants and complex food or environmental matrices.

Conclusion


The Strata Melamine SPE combined with ultra-fast LC/MS/MS or rapid GC/MS methods enables reliable, high-throughput quantitation of melamine and cyanuric acid in food and tissue samples. The protocol delivers robust recoveries, low detection limits, and significant time savings, supporting regulatory compliance and quality control.

Reference


  1. Litzau J, Mercer G, Mulligan K. GC-MS Method for Melamine and Cyanuric Acid. U.S. FDA CVM Laboratory Information Bulletin, 2007.
  2. Tosoh Bioscience. TSK-GEL Amide-80 HILIC Columns for Melamine and Cyanuric Acid Analysis in Milk by LC-MS/MS; Application Note AN191108.
  3. U.S. Food and Drug Administration. Guidance for Industry: Bioanalytical Method Validation; CDER/CVM, 2001.
  4. World Health Organization. Toxicological and Health Aspects of Melamine and Cyanuric Acid; WHO Expert Meeting Report, 2009.

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