2016
DOI: 10.4172/2161-0495.1000315
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Toxicity and Genotoxicity of Beauty Products on Human Skin Cells In Vitro

Abstract: Background:We use beauty products in high quantities every day and in the process, we are exposed to a wide variety of chemicals used in these products. These chemicals are a particularly insidious form of body pollution because they enter the human body through multiple routes. The problem with commercial products and particularly beauty products is that millions of people apply beauty products to their skin daily for long time.Objective: To determine the toxicity and genotoxicity effects of four facial beaut… Show more

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Cited by 10 publications
(5 citation statements)
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References 32 publications
(40 reference statements)
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“…Fluorescent SWNTs have recently been employed to build sensor arrays capable of detecting protein efflux from microorganisms and synthetic scaffolds for biosensing devices . Therefore, in order to study the functionality, biocompatibility, and cell toxicity of our hybrid material 3 , standard cell proliferation assays such as MTT and crystal violet assays were carried out by using human prostate cancer (PC‐3) and healthy human dermal fibroblasts (FEK4) cell lines. PC‐3 and FEK4 cells were incubated with the hybrid material 3 (glucan@CdSe[CdSe@SWNTs]), CdSe[CdSe@SWNTs] composites, and β‐ d ‐glucan for 48 h at 37 °C under normoxia (21 % O 2 and 5 % CO 2 , Figure ) and induced acute hypoxia conditions using standard CoCl 2 .6 H 2 O based assays (Figure ).…”
Section: Resultsmentioning
confidence: 99%
“…Fluorescent SWNTs have recently been employed to build sensor arrays capable of detecting protein efflux from microorganisms and synthetic scaffolds for biosensing devices . Therefore, in order to study the functionality, biocompatibility, and cell toxicity of our hybrid material 3 , standard cell proliferation assays such as MTT and crystal violet assays were carried out by using human prostate cancer (PC‐3) and healthy human dermal fibroblasts (FEK4) cell lines. PC‐3 and FEK4 cells were incubated with the hybrid material 3 (glucan@CdSe[CdSe@SWNTs]), CdSe[CdSe@SWNTs] composites, and β‐ d ‐glucan for 48 h at 37 °C under normoxia (21 % O 2 and 5 % CO 2 , Figure ) and induced acute hypoxia conditions using standard CoCl 2 .6 H 2 O based assays (Figure ).…”
Section: Resultsmentioning
confidence: 99%
“…Next the MTT solution was mixed and incubated up to 4 h, then DMSO was added and gently shaken for 5–15 min. Absorbance was noted at 570 nm and cell viability was determined via Equation (4) [ 37 ]. …”
Section: Methodsmentioning
confidence: 99%
“…In the case of cosmetic products, considering the specific route of topical application, the in vitro cytotoxicity testing on skin cell lines (in particular keratinocytes and fibroblasts) can be used for primary toxicological evaluation of new ingredients such as surfactants, colorants, preservatives, and additives. 2,[23][24][25] In this study, the human keratinocyte (HaCaT cell line) was used for evaluation of the Monascus pigments skin toxicity by using in vitro MTT assay. The results of the cytotoxicity of Monascus pigments against normal human keratinocytes were shown in Table 2 which indicated that Monascus pigments are nontoxic toward the normal skin cell in the in vitro study.…”
Section: Human Erythrocytes Cytotoxicity Assaymentioning
confidence: 99%
“…However, increasing side effects of some sunscreen components has made it indispensable to search for natural photoprotectants. 2 The most commonly utilizing sunscreen ingredients such as oxybenzone linked to sun exposure triggered allergic reactions, generating free radicals, which may be associated with cell damages. 3,4 While the nanoscale TiO 2 and ZnO are responsible for the generation of a substantial amount of reactive oxygen species, which upon UV illumination causes modifications in nucleic acid bases and eventually cell death.…”
mentioning
confidence: 99%