Analysis of Suspected Flavor and Fragrance Allergens in Perfumes Using Two-Dimensional GC with Independent Column Temperature Control Using an LTM Oven Module
Applications | 2009 | Agilent TechnologiesInstrumentation
Perfume and fragrance allergens such as limonene, citral and cinnamic aldehyde can cause skin irritation and must be labeled when exceeding regulatory thresholds in cosmetic products. Complex sample matrices and wide concentration ranges make reliable qualitative and quantitative analysis challenging.
The main goal of the study is to develop and demonstrate a multidimensional gas chromatography–mass spectrometry (2D GC/MS) method that uses Deans switch heartcutting and an independent low thermal mass (LTM) second column oven to achieve optimal separation and quantification of 31 regulated allergens in complex perfume samples.
The method employs an Agilent 7890A GC coupled to a 5975 MSD, with a Deans switch for heartcutting and a capillary flow module, plus an LTM oven module for second-dimension column temperature control. The primary column is an HP-5MS 30 m × 0.25 mm id × 0.25 µm, while the secondary column is a DB-17ms 30 m × 0.25 mm id × 0.25 µm housed in the LTM module. Perfume samples were diluted in acetone and injected in split mode. Three heartcut windows targeted coeluting allergens. GC and LTM ovens were programmed independently to focus and then separate analytes under optimized temperature ramps.
One-dimensional GC/FID could not resolve coeluting allergens in complex perfume matrices. Heartcutting transferred critical elution windows to the LTM column, where independent temperature programming improved selectivity and resolution. For example, the two lyral isomers were fully resolved only when the LTM oven was held at 50 °C during cuts and then ramped at 6 °C/min. Over 20 compounds spanning a wide volatility and concentration range were cleanly separated and quantified.
The described 2D GC/MS method offers:
Future developments may include integration of chiral second-dimension columns for enantiomeric purity analysis, automation of heartcutting strategies based on real-time data, and coupling to high-resolution MS for non-target screening. The approach is broadly applicable to other complex matrices in food, environmental and pharmaceutical analysis.
Two-dimensional GC with Deans switch heartcutting and an independent LTM oven module significantly improves the separation and quantitation of regulated flavor and fragrance allergens in complex perfume and cosmetic matrices. The method enhances selectivity, reduces matrix interferences, and meets regulatory requirements.
1. Directive 2003/15/EC, Official Journal of the European Union, 2003.
2. Chaintreau et al., J. Agric. Food Chem. 51 (2003) 6398–6403.
3. David et al., LC·GC Europe 19 (2006) 602–616.
4. Leijs et al., J. Agric. Food Chem. 53 (2005) 5487–5491.
5. Luan et al., Agilent Technologies publication 5989-8724EN (2008).
6. David & Klee, Agilent Technologies publication 5990-3428EN (2009).
7. David & Klee, Agilent Technologies publication 5989-6460EN (2007).
GC/MSD, GC/SQ
IndustriesOther
ManufacturerAgilent Technologies
Summary
Significance of the Topic
Perfume and fragrance allergens such as limonene, citral and cinnamic aldehyde can cause skin irritation and must be labeled when exceeding regulatory thresholds in cosmetic products. Complex sample matrices and wide concentration ranges make reliable qualitative and quantitative analysis challenging.
Study Objectives and Overview
The main goal of the study is to develop and demonstrate a multidimensional gas chromatography–mass spectrometry (2D GC/MS) method that uses Deans switch heartcutting and an independent low thermal mass (LTM) second column oven to achieve optimal separation and quantification of 31 regulated allergens in complex perfume samples.
Methodology and Used Instrumentation
The method employs an Agilent 7890A GC coupled to a 5975 MSD, with a Deans switch for heartcutting and a capillary flow module, plus an LTM oven module for second-dimension column temperature control. The primary column is an HP-5MS 30 m × 0.25 mm id × 0.25 µm, while the secondary column is a DB-17ms 30 m × 0.25 mm id × 0.25 µm housed in the LTM module. Perfume samples were diluted in acetone and injected in split mode. Three heartcut windows targeted coeluting allergens. GC and LTM ovens were programmed independently to focus and then separate analytes under optimized temperature ramps.
Key Results and Discussion
One-dimensional GC/FID could not resolve coeluting allergens in complex perfume matrices. Heartcutting transferred critical elution windows to the LTM column, where independent temperature programming improved selectivity and resolution. For example, the two lyral isomers were fully resolved only when the LTM oven was held at 50 °C during cuts and then ramped at 6 °C/min. Over 20 compounds spanning a wide volatility and concentration range were cleanly separated and quantified.
Benefits and Practical Applications
The described 2D GC/MS method offers:
- Enhanced resolution for coeluting flavor and fragrance allergens compared to 1D GC.
- Independent optimization of second-column temperature for improved selectivity.
- Accurate identification and quantitation in complex matrices at regulatory levels.
- Flexibility to backflush nonvolatile interferences in finished products.
Future Trends and Potential Uses
Future developments may include integration of chiral second-dimension columns for enantiomeric purity analysis, automation of heartcutting strategies based on real-time data, and coupling to high-resolution MS for non-target screening. The approach is broadly applicable to other complex matrices in food, environmental and pharmaceutical analysis.
Conclusion
Two-dimensional GC with Deans switch heartcutting and an independent LTM oven module significantly improves the separation and quantitation of regulated flavor and fragrance allergens in complex perfume and cosmetic matrices. The method enhances selectivity, reduces matrix interferences, and meets regulatory requirements.
References
1. Directive 2003/15/EC, Official Journal of the European Union, 2003.
2. Chaintreau et al., J. Agric. Food Chem. 51 (2003) 6398–6403.
3. David et al., LC·GC Europe 19 (2006) 602–616.
4. Leijs et al., J. Agric. Food Chem. 53 (2005) 5487–5491.
5. Luan et al., Agilent Technologies publication 5989-8724EN (2008).
6. David & Klee, Agilent Technologies publication 5990-3428EN (2009).
7. David & Klee, Agilent Technologies publication 5989-6460EN (2007).
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