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High Throughput Analysis of Phthalates and Parabens in Cosmetics and Personal Care Products Using UPLC with Mass Detection and Empower 3 Software

Applications | 2015 | WatersInstrumentation
LC/MS, LC/SQ
Industries
Other
Manufacturer
Waters

Summary

Importance of the Topic


The widespread use of phthalates, parabens, and triclocarban in cosmetics and personal care products has raised health and regulatory concerns due to potential endocrine disruption, allergenic effects, and links to cancer. High-throughput, sensitive, and reliable analytical methods are essential for routine screening and compliance with regulations such as the EU Cosmetics Directive 1223/2009.

Objectives and Study Overview


This study aimed to develop and validate a rapid UPLC-MS method for simultaneous identification and quantification of key phthalates, parabens, and triclocarban in cosmetic and personal care matrices. Emphasis was placed on reducing analysis time and solvent consumption while maintaining high sensitivity and selectivity.

Methodology and Instrumentation


Sample Preparation
  • Weighed 0.2 g of sample was extracted with 2.5 mL water and 2.5 mL methanol.
  • Vortex mixing (2 min, 1 600 rpm) followed by ultrasonic extraction (30 min).
  • Centrifugation (10 000 rpm, 5 min) and transfer of supernatant to LC vials.
Chromatographic Conditions
  • System: ACQUITY UPLC H-Class with BEH C18 column (2.1 × 50 mm, 1.7 μm).
  • Gradient from 30%A (water/0.1% formic acid) to 90%B (methanol/0.1% formic acid) over 5 min.
  • Flow rate 0.6 mL/min, column at 40 °C, sample at 10 °C, injection volume 5 μL.
Mass Spectrometry
  • Detector: ACQUITY QDa with ESI in positive and negative mode.
  • Capillary voltage 0.8 kV, probe temperature 450 °C.
  • Selected Ion Recording for each analyte ensured specificity.
Data Processing Empower 3 CDS software controlled acquisition and automated quantitation.

Main Results and Discussion


The UPLC-MS method achieved baseline separation of key isomeric phthalates (DiBP vs. DiNP, DEHP vs. DnOP) in a total runtime of 5 min. Calibration curves were linear (R2>0.99) over 0.01–10 µg/mL for phthalates and triclocarban, and 0.05–25 µg/mL for parabens. The workflow reduced analysis time by over seven-fold and solvent usage by more than 90% compared to conventional HPLC and GC methods.

Benefits and Practical Applications


  • High throughput enables rapid screening in quality-control laboratories.
  • Reduced solvent consumption lowers operational costs and environmental impact.
  • Mass detection provides unequivocal compound confirmation, improving regulatory compliance.
  • Robust performance suits both method development and routine analysis.

Future Trends and Applications


The method framework can be extended to additional emerging cosmetic contaminants and complex matrices. Integration with automated sample handling and advanced data analytics will further enhance throughput and decision support. Ongoing developments in miniaturized MS detectors and greener solvent systems promise even more sustainable workflows.

Conclusion


A five-minute UPLC-MS method combining ACQUITY UPLC H-Class, QDa detection, and Empower 3 software has been validated for simultaneous analysis of phthalates, parabens, and triclocarban in personal care products. The approach delivers rapid, sensitive, and cost-effective quantitation with high confidence, meeting current regulatory needs.

References


  1. Darbe PD. Environmental oestrogens, cosmetics and breast cancer. Best Practice & Research Clinical Endocrinology & Metabolism. 20(1):121–143, 2006.
  2. Golden R, Gandy J, Vollmer G. Review of the endocrine activity of parabens and implications for potential risks to human health. Critical Reviews in Toxicology. 35(5):435–458, 2005.
  3. European Parliament and Council. Regulation (EC) No 1223/2009 on Cosmetic Products. Official Journal of the European Union L342:59–209, 2009.
  4. Shen HY et al. Simultaneous determination of phthalates and parabens in cosmetic products using HPLC-DAD and GC-MS. J Sep Sci. 30:48–54, 2007.
  5. Farajzadeh MA et al. Dispersive liquid-liquid microextraction of parabens for GC-FID determination. Talanta. 81:1360, 2010.
  6. Labat L et al. HPLC vs capillary zone electrophoresis for parabens in cosmetics. J Pharm Biomed Anal. 23:763, 2000.
  7. González-Mariño I et al. LC-QTOF-MS analysis of parabens in wastewater. Water Research. 20:6770–6780, 2011.
  8. Wang Y et al. SPE-HPLC-ESI-MS determination of triclocarban in environmental water. J Geoscience and Environment Protection. 1(2):13–17, 2013.

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