SKIN PROTECTION 123 Active with 1% IBR-UrBioTect Placebo 10.0 N.S 5.0 0.5 0.0 D14 -0.5 -.10.0 -8.8 * -0.3 D28 7.2
14.0 12.0 10.0 8.0 6.0 4.0 2.0 0.0
12.7 N.S Active with 1% IBR-UrBioTect Placebo 12.5 *
3.1 1.9
D14 Figure 2:Wrinkle count variation.
meaningful increase in ITA (up to 25% at D28), with statistical significance vs. study D0 and vs. the placebo. The effect is shown to progressively build up over the course of the study.
Helps repair wrinkles in a smoking environment Visia-CA image analysis data show that daily application of the active product results in a reduction in wrinkle counts after 28 days, statistically significant vs. D0 and vs. the placebo.
Improves skin elasticity in a smoking environment
Cutometer data shows that daily application of the active product results in a meaningful improvement in skin elasticity after 28 days, statistically significant vs. D0 and vs. the placebo. Here again, the effect is shown to build up over the course of the study (the improvement is already visible but has not yet acquired statistical significance, at D14).
0.0 -0.5 -0.10 -15.0 -20.0 -20.2 -25.0 -30.0 Figure 4: TEWL malar evolution. April 2018 Active with 1% IBR-UrBioTect Placebo -17.8 * * -7.8 -7.3 Figure 3: Elasticity (R2) variation periorbital.
Enhances skin barrier function in a smoking environment Trans Epidermal Water Loss (TEWL) data shows that daily application of the active product results in a rapid and meaningful improvement in skin barrier function, as expressed by a reduction in trans- epidermal water loss after 14 days, with statistical significance vs. D0 and vs. the placebo. The effect is maintained at D28.
Illustrative images
The illustrative photographs in Figure 5 demonstrate the reduction in the appearance of wrinkles and the improvement in skin tone resulting from daily application of the active product.
Protects from heavy metals: chelation (Rohman et al.2010) Following on the clinical results described above, and in order to begin providing mechanistic explanations for the effects observed, the chelating power of Inula
helenium extract, was evaluated according to the method described in Rohman et al. (2010). In this method, the ferrous ion is used as a model for heavy metals. The concentration of the ferrous iron-Ferrozine complex is measured by spectrophotometry (absorbance at 562 nm). Addition of a chelator, capturing iron away from said complex, results in a drop in the measured absorption. EDTA was used as positive control and comparison point. Chelating power is expressed as an IC50 value (mg/ml), being the concentration of tested product at which 50% of available iron was chelated. In this model, an Inula helenium extract was shown to have an IC50 of 0.54 mg/mL (expressed on a dry weight basis), indicating that the product possesses chelating power, ca. 1 order of magnitude below that of reference chelator EDTA on a dry weight basis, measured at 0.038 mg/mL.
Detoxifying and pre-biotic benefits Detoxifying and some pre-biotic benefits were shown with Dunaliella salina cell culture as a model for evaluating the anti- pollution effect. To further expand the scope of our investigations into the detoxifying potential of Inula helenium extract, we used the microalgae, Dunaliella salina as an animal- and human-free model to demonstrate the product’s efficacy. The unicellular alga Dunaliella salina was selected as a sensitive, reliable, and cost effective model system for evaluating the protective effects of an Inula helenium extract against exogenous toxins. Algae, and micro algae specifically, are commonly used as a sensitive model system to evaluate water quality. Dunaliella cultures were incubated with Inula helenium extract at concentrations of
PERSONAL CARE EUROPE
D28
% change (%) from D0
% change (%) from D0
% change (%) from D0
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