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Automated DMI for screening of cosmetic products

Applications | 2006 | Agilent TechnologiesInstrumentation
GC/MSD, GC/SQ
Industries
Other
Manufacturer
Shimadzu, GL Sciences

Summary

Significance of the Topic


The analysis of cosmetic products presents significant challenges due to complex water–oil emulsions and low target analyte concentrations. Difficult Matrix Introduction (DMI) via programmable temperature vaporisation (PTV) offers a streamlined route for direct injection of minute sample aliquots, eliminating laborious extraction and cleanup steps while preserving analytical integrity.

Objectives and Study Overview


This study demonstrates the application of DMI–GC/MS for rapid screening, identification and quantification of known and unknown ingredients in a range of cosmetic formulations, including lipsticks, lotions, washing powders and shampoos, without conventional sample preparation.

Methodology and Instrumentation


The DMI approach uses a small sample (8–12 mg) sealed in a microvial automatically introduced into an OPTIC 3 PTV injector (ATAS GL Int’l). The injector is heated to desorb volatile analytes onto a GC column while non-volatiles remain in the vial. The system comprises:
  • GCMS-QP2010 mass spectrometer (Shimadzu)
  • PTV OPTIC 3 injector with automated liner exchanger (LINEX, ATAS GL)
  • PHASER sniffing port in parallel with MS detector
  • Inertcap wax column (0.32 mm × 60 m, 0.5 μm film)
  • Helium carrier gas

Typical temperature programs:
  • Washing powder: 40 °C (6.3 min), 15 °C/min to 130 °C, 3 °C/min to 250 °C (25 min hold)
  • Shampoo: 35 °C (8 min), 5 °C/min to 230 °C (10 min hold)

Main Results and Discussion


Repeatability (n = 10) for washing powder analysis showed retention time RSDs below 4 % and peak area RSDs below 10 %. Total ion chromatograms revealed consistent profiles across runs. In shampoo screening, 16 major fragrance compounds and allergens (e.g., d-limonene, linalool, citronellol) were identified and quantified in a single DMI–GC/MS run, demonstrating effective allergen surveillance without prior cleanup.

Benefits and Practical Applications


The PTV-DMI method:
  • Eliminates extensive sample preparation
  • Minimizes matrix contamination and column fouling
  • Enables rapid screening and quantification of trace components
  • Supports quality control in cosmetic, personal care and regulatory environments

Future Trends and Potential Applications


Emerging directions include full automation of DMI workflows, integration with advanced olfactometric detection, extension to other challenging matrices (environmental, food) and coupling with high-resolution mass spectrometry and chemometric data analysis for deeper compound profiling.

Conclusion


DMI coupled with GC/MS and sniffing port provides a robust, reproducible and efficient platform for comprehensive analysis of cosmetic matrices, offering significant advantages in speed, sensitivity and maintenance reduction.

References


  • A. Amirav and S. Dagan, Europ. Mass Spectrom. 3, 105–111 (1997)
  • ATAS GL International, De Run 4441, 5500 AA Veldhoven, The Netherlands
  • University of Amsterdam, van’t Hoff Institute for Molecular Sciences, Nieuwe Achtergracht 166, 1018 WV Amsterdam, The Netherlands

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