A methodological approach for quantifying aerial formaldehyde released by some hair treatments-modeling a hair-salon environment.

Formaldehyde is a well-known toxic agent, therefore having a highly regulated status. Despite, some cosmetic firms recently introduced high and illegal concentrations of formaldehyde in hair treatments for increasing straightening and long-lasting performances. The objective of this study was to assess how and to which extent, these products may disperse formaldehyde in the environment of a hair salon, possibly exposing the consumer and the hair professional technician to hazardous airborne amounts of formaldehyde. A laboratory room was equipped with three air pumps located at three locations: close to the heads of a mannequin, nearby the hair technician and the whole volume of the room. Pumps were connected to cartridges apt at trapping airborne formaldehyde. The latter was further quantified through an HPLC procedure.As compared to hair treatments free from formaldehyde that do not modify the airborne formaldehyde levels, products with a high concentration of formaldehyde (1.7% and 9.3%) disperse this compound in the environment to a high and hazardous concentration, detrimental to both consumer and hair professional. The brushing procedure on the hair led to a much higher dispersion of airborne formaldehyde than the hair straightening/ironing technique. To conclude, the use of hair treatments that contain high and illegal amounts of formaldehyde creates a hazardous environment to all people present within a hair salon.Implications: This methodology adopted here might be used to evaluate during conception phase the level of Formaldehyde release and be used as part of safety data for the registration. However, the present work also strongly promotes the adoption of electronic detectors (commercially available) that continuously record the aerial concentration of Formaldehyde, when dealing with hair styling products that contain legal or illegal (> 0.2%w/w) content of Formaldehyde These detectors not only cover an adequate and realistic range of aerial Formaldehyde but can be used and transported at different locations of a given space. Such a cautious measure comes from common sense as it relates to the health status of consumers and operators present in a hair salon environment.

Evaluation of the cytotoxicity effect of dimethyl sulfoxide (DMSO) on Caco2/TC7 colon tumor cell cultures.

Dimethyl sulfoxide (DMSO) is usually used to solubilize poorly soluble drugs in permeation assays such as that using Caco2 enterocyte-like cells. The objective of this study was to evaluate the toxicity of DMSO on Caco2/TC7 cells and determinate the maximal concentration usable in permeation experiments. Caco2/TC7 cells were cultured for 21 d on 96-well plates for evaluation of toxicity. The determination of lactate dehydrogenase (LDH) release in cell supernatant and the measurement of Neutral Red (NR) uptake are used for cytotoxicity assays. DMSO solutions (0-100%) in Hank's balanced salt solution containing HEPES (25 mM), pH 7.4, were incubated with Caco-2/TC7 cells on 96 well plates. Caco2/TC7 cells were cultured on Transwell-Clear inserts to evaluate the influence of DMSO on the apparent permeability of the paracellular marker mannitol. DMSO 10% did not induce any significant increase in LDH release whereas a significant increase in LDH activity (ANOVA, p<0.05) occurred at a DMSO concentration of 20 to 50%. NR incorporation in viable cells was statistically reduced by 27 to 36% at DMSO concentration of 20% up to 100% (ANOVA, p>0.05). No statistical difference (p<0.05) in apparent mannitol permeability was observed between the control and 10% DMSO groups. In conclusion, at concentrations of up to 10%, DMSO did not produce any significant alteration in apical membrane permeability or on cell-to-cell tight junctional complexes.

Short term Caco-2/TC7 cell culture: comparison between conventional 21-d and a commercially available 3-d system.

The Caco-2 cell model is a valuable tool for studying intestinal biotransformation of xenobiotics and to evaluate the potential of human intestinal absorption of new compounds. These properties were evaluated with Caco-2/TC7 cells in accelerated conditions to reduce maturation lag time from 21-d to 3-d in order to increase time and labor efficiency. Transmission electron and fluorescent microscopy were used for morphological characterization. Alkaline phosphatase and lactate dehydrogenase activities were assessed within time. Cytochrome P450 expression was studied by RT-PCR. Apparent permeabilities of a set of passively absorbed molecules across Caco-2/TC7 cell monolayers were determined to evaluate potential of both systems for prediction of human intestinal absorption. Microscopic images revealed that cells under both conditions differentiated as enterocyte-like cells but did so heterogeneously in the 3-d model. TEER values have shown that the 3-d model is a leakier cell system with higher mannitol Papp (cm/s). Biochemical characterization (hydrolase activities, CYP450 expression) suggested that the 3-d model was at a lower maturation level than the 21-d model. Carrier-mediated uptake of L-Phe was lower in the 3-d model suggesting that this model has limited application for mechanistic studies. Reasonable correlation was obtained between the two models (r2=0.88, p>0.01) for 11 passively absorbed compounds with high potential of rank ordering of compounds. Although results suggested that the 3-d cells are under-differentiated, they could be usable to estimate the oral absorption of passively absorbed compounds.