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Differentiation of cellular responses to particulate and soluble constituents in sunscreen products

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

Despite the growing awareness of potential human and environmental risks associated with sunscreens, identifying the specific constituents responsible for their potential toxicity is challenging. In this study, we applied three different types of sunscreens with contrasting compositions and compared the effects of their particulate and soluble fractions based on 15 cellular biomarkers of HaCaT cells. Multilinear regression analysis revealed that the internalized soluble fractions played a primary role in the overall cytotoxicity of sunscreen mixtures, which was primarily attributed to their biotransformation, generating metabolites with higher toxicity. The presence of plastic microspheres in sunscreens either inhibited the internalization of soluble fractions or led to their redistribution toward lysosomes. Conversely, subcellular toxicity resulting from the sunscreen mixture was predominantly influenced by particulates. Bio-transformable particulates such as ZnO dissolved in the organelles and induced higher subcellular toxicity compared to bioinert particulates such as microplastics. Subcellular biomarkers including lysosomal count, lysosomal size, mitochondrial count and mitochondrial shape emerged as the potential predictors of sunscreen presence. Our study provides important understanding of sunscreen toxicity by elucidating the differential impacts of particulate and soluble fractions in mixture contaminants. © 2024 Elsevier B.V.
Original languageEnglish
Article number134791
JournalJournal of Hazardous Materials
Volume474
Online published2 Jun 2024
DOIs
Publication statusPublished - 5 Aug 2024

Funding

We thank the anonymous reviewers for their comments. This study was supported by the Shenzhen Municipal Science and Technology Innovation Commission ( JCYJ20220818101202006 ), and Hong Kong Research Grants Council (CityU 11103022 ) and the National Science Foundation of China ( 22276157 ).

Research Keywords

  • Biomarker
  • Microplastic
  • Subcellular toxicity
  • Toxicity identification and evaluation
  • Zinc oxide

RGC Funding Information

  • RGC-funded

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