In vitro cytotoxicity and phototoxicity study of cosmetics colorants
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
21570462
DOI
10.1016/j.tiv.2011.04.026
PII: S0887-2333(11)00122-6
Knihovny.cz E-resources
- MeSH
- Coloring Agents toxicity MeSH
- Cell Death drug effects MeSH
- BALB 3T3 Cells MeSH
- NIH 3T3 Cells MeSH
- Fluorescence MeSH
- Fluorometry methods MeSH
- Dermatitis, Phototoxic etiology MeSH
- Cosmetics chemistry toxicity MeSH
- Humans MeSH
- Mitochondrial Membranes drug effects metabolism MeSH
- Mice MeSH
- Hydrogen Peroxide metabolism MeSH
- Reactive Oxygen Species metabolism MeSH
- Toxicity Tests methods MeSH
- Ultraviolet Rays MeSH
- Cell Survival MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Coloring Agents MeSH
- Cosmetics MeSH
- Hydrogen Peroxide MeSH
- Reactive Oxygen Species MeSH
The aim of the work was early identification of preventable risk factors connected with the consumers usage of products of everyday use, such as cosmetics, toys and children products, and other materials intended for contact with human skin. The risk factor is represented by substances with irritation potential and subsequent possible sensitisation, resulting in negative impact on human physical and psychical health with social and societal consequences. The legislation for cosmetics, chemical substances and other products requires for hazard identification the application of alternative toxicological methods in vitro without the use of animals. For this reason we used a battery of alternative assays in vitro, based on cell cultures. Progressive methods of molecular biology, based on fluorimetry and fluorescence, were employed for identification of early morphological and functional changes on cellular level. Four colorants frequently used in cosmetics (P-WS Caramel, Chlorophyllin, Unicert Red K 7054-J and Unicert Red K 7008-J) were tested on cell line NIH3T3 (mouse fibroblast cell) and 3T3 Balb/c with/without UV irradiation (dose 5 J cm(-2)). Fluorescence methods for the study of cell damage using fluorescence probes offer results for the evaluation of cytotoxicity and cell viability of adherent cells. We detected intracellular production of ROS investigated by molecular probe CM-H(2)DCFDA, which is primarily sensitive to the increased production of hydrogen peroxide or its downstream products. Toxic effects on the cellular level were identified by viability tests using Neutral Red uptake and MTT assay, where the live cells reduce yellow soluble 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) to insoluble formazan crystals. The reaction was investigated on mitochondrial membrane of living cells and the type of cell death was determined using Apoptosis detection kit. Cytotoxicity tests revealed health risks of using Chlorophyllin and Unicert Red K 7054-J.
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