• Application Note

Method Equivalence Testing for Sunscreen Actives Using the ACQUITY UPLC H-Class PLUS System and ACQUITY UPLC H-Class System

Method Equivalence Testing for Sunscreen Actives Using the ACQUITY UPLC H-Class PLUS System and ACQUITY UPLC H-Class System

  • Michael Jones
  • Waters Corporation
Applying sun lotion

This is an Application Brief and does not contain a detailed Experimental section.

Abstract

This application brief demonstrates superior performance of the ACQUITY UPLC H-Class PLUS System with UV and mass detection for accurate recording of method development activities towards efficient separation, detection, and quantitation of sunscreen actives.

Benefits

The ACQUITY UPLC H-Class Plus System coupled to Empower 3 CDS Software offers powerful tools to streamline method development activities.

Introduction

Skin cancer is the most common type of cancer diagnosed in the U.S.; it is estimated one in five Americans will develop skin cancer in their lifetime.1-4 The most serious class of skin cancer is the melanomas, which develop in the melanocyte cells of skin. The World Health Organization (WHO) estimates 65,000 mortalities per year are attributed to melanomas.5 Around 95% of melanomas are caused by exposure to UV radiation.6

Due to the damaging effects of UV light on skin, increasing numbers of cosmetics and personal care products are formulated with chemicals that actively filter out UV radiation. However long term contact with chemical sunscreens may increase the risk of developing a skin allergy to sunlight.7 For this reason, the type and amount of sunscreen agents in formulations have been strictly regulated around the world and effective methods for simultaneously detecting multiple chemical sunscreen agents in formulations are necessary.8 HPLC has been applied extensively to this application.9 However, drawbacks associated with the methods published to date include prohibitive analysis times on HPLC scale columns and/or the use of toxic solvents.

In this technology brief, we demonstrate equivalent performance of Waters ACQUITY UPLC H-Class PLUS System for the separation and detection of a mix of six chemical UV filters by measuring and comparing typical system suitability parameters to the data acquired on an ACQUITY UPLC H-Class System on two different column chemistries.

Results and Discussion

Analytical standards were purchased from Sigma-Aldrich Ltd (Poole, Dorset, UK). The standards were prepared at concentrations of 25 µg/mL in 60:40 water:MeOH for UPLC analysis. UPLC separation was achieved on the ACQUITY UPLC HSS PFP Column (1.8 µm, 2.1 x 50 mm, p/n: 186005965) and the ACQUITY UPLC BEH C8 Column (1.7 µm, 2.1 x 50 mm, p/n: 186002877) at a flow rate of 0.5 mL/min using a general gradient: 40% B initially to 1 min grading to 95% B at 4.5 min, followed by a 2.5 min hold before returning to 40% B and re-equilibrating for 1 min. The mobile phase consisted of A: water and B: methanol, each with 0.1% formic acid, and the injection volume was 5 µL. The retention times and peak areas were measured by Empower 3 CDS Software and were the average of five replicate injections.

Six sunscreen actives were analyzed on both column chemistries using the same mobile phase, gradient, and injection volume by both the ACQUITY UPLC H-Class and the ACQUITY UPLC H-Class PLUS systems. Figure 1 shows chromatograms for the six compounds on both systems using the ACQUITY UPLC BEH C8 Columns. Figure 2 shows the same six analytes separated using ACQUITY UPLC HSS PFP Column across both systems. The retention times and peak areas between the two systems, shown in Figure 3, were comparable for all of the compounds tested. Retention time reproducibility as illustrated by %RSD was less than 0.2% and 0.04% for the ACQUITY UPLC H-Class and ACQUITY UPLC H-Class PLUS systems respectively. These data demonstrate the reproducibility across the ACQUITY UPLC H-Class and H-Class PLUS systems and show that methods previously validated on the ACQUITY UPLC H-Class systems should not need revalidating for performing analyses on the ACQUITY UPLC H-Class PLUS System.

Overlaid chromatograms of individual sunscreen standards, separated by ACQUITY UPLC BEH C8 Column.
Figure 1. Overlaid chromatograms of individual sunscreen standards, separated by ACQUITY UPLC BEH C8 Column chemistry on both the ACQUITY UPLC H-Class and ACQUITY UPLC H-Class PLUS systems.
Overlaid chromatograms of individual sunscreen standards, separated using the ACQUITY UPLC HSS PFP Column.
Figure 2. Overlaid chromatograms of individual sunscreen standards, separated using the ACQUITY UPLC HSS PFP Column on both the ACQUITY UPLC H-Class and ACQUITY UPLC H-Class PLUS systems.
Representative retention time and peak area data.
Figure 3. Representative retention time and peak area data for the ACQUITY UPLC H-Class and ACQUITY UPLC H-Class PLUS systems.

Conclusion

The ACQUITY UPLC H-Class PLUS System is a robust and reliable analytical technology for the accurate analysis of sunscreen actives in cosmetic formulations. The enhanced reproducibility of the system will aid in the identification of batch to batch variations in QC monitoring of sunscreen manufacture. 

References

  1. Guy GP, Thomas CC, Thompson T, Watson M, Massetti GM, Richardson LC. Vital signs: Melanoma incidence and mortality trends and projections–United States, 1982–2030. MMWR Morb Mortal Wkly Rep. (2015); 64(21):591–596.
  2. Guy GP, Machlin S, Ekwueme DU, Yabroff KR. Prevalence and costs of skin cancer treatment in the US, 2002–2006 and 2007–2011. Am J Prev Med. (2015); 48:183–7.
  3. Stern RS. Prevalence of a history of skin cancer in 2007: results of an incidence-based model. Arch Dermatol. (2010); Mar;146(3):279-82.
  4. Robinson JK. Sun Exposure, Sun Protection, and Vitamin D. JAMA 2005; 294: 1541-43.
  5. World Health Organization, Solar ultraviolet radiation: Global burden of disease from solar ultraviolet radiation. Environmental Burden of Disease Series, N.13. (2006).
  6. Islami F et al. Proportion and number of cancer cases and deaths attributable to potentially modifiable risk factors in the United States. CA Cancer J Clin. Published online Nov. 21, 2017. doi: 10.3322/caac.21440.
  7. He QS, Xu, N, Liao SF. Determination of 12 Sunscreen Agents in Cosmetics by High Performance Liquid Chromatography. Chin. J. Chromatogr. (2011); 29: 762–767.
  8. Pirotta G. Household and Personal Care Today. (2015); 10(4): 19–24.
  9. Salvador A, Chisvert A. Sunscreen Analysis: A Critical Survey on UV Filters Determination. Anal Chim Acta. (2005); 537(1): 1–14.

720006283, May 2018

Back To Top Back To Top