Back to Journals » Clinical, Cosmetic and Investigational Dermatology » Volume 11

In vivo validation of the multicomponent powder (Vitachelox®) against the deposition of polluting ions

Authors Giacomelli L, Togni S, Meneghin M, Eggenhöffner R , Maramaldi G

Received 7 November 2017

Accepted for publication 17 January 2018

Published 8 March 2018 Volume 2018:11 Pages 109—113

DOI https://doi.org/10.2147/CCID.S156324

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Jeffrey Weinberg



Luca Giacomelli,1 Stefano Togni,2 Martino Meneghin,2 Roberto Eggenhöffner,1 Giada Maramaldi2

1Department of Surgical Science and Integrated Diagnostics, University of Genoa, Genoa, Italy; 2Indena S.p.A, Milan, Italy


Purpose: The purpose of this in vivo study is to evaluate the acute clinical application of a multicomponent powder (Vitachelox®), including three naturally occurring standardized extracts rich in polyphenols (grape seed extract, green tea extract, oak wood/bark extract), on healthy volunteers by measuring prevention of any metal deposition within the stratum corneum (SC) following a 6-h exposure period in a polluted environment.
Patients and methods: In this in vivo study, we evaluated the skin protective activity of the multicomponent powder formulated in a base emulsion compared to a relevant placebo cream. Using the tape stripping method, SC samples of face skin obtained from 30 healthy volunteers were compared following a 6-h exposure in a polluted area.
Results: No statistically significant variations on the amount of heavy metals were found in the samples of SC cells obtained from the hemi-faces treated with the multicomponent powder, with respect to baseline. On the contrary, a significantly higher concentration of heavy metals was found in the cells samples obtained from the hemi-faces treated with the placebo cream. In particular, an increased concentration of heavy metals superior to 100% were found for iron and zinc (+130.2% and +142.6%, respectively; p<0.001).
Conclusion: This in vivo study validates and extends previous in vitro findings, indicating that the multicomponent powder allows the prevention of any metal deposition within the SC following exposure in a polluted environment. Our results suggest that the test product could play an effective role in counteracting skin damages induced by air pollution.

Keywords: air pollution, heavy metals, oxidative stress, polyphenols, green tea extract, oak wood extract, grape seed extract, antipollution, stratum corneum

Introduction

Exposure to indoor and outdoor air pollution represents a major public health concern.13 Most studies focusing on air pollution effects on the lung and the cardiovascular system have shown that air pollutants are linked to heart diseases, respiratory infections, and lung cancer.4 More recently, epidemiological and mechanistic studies suggest that air pollution is also affecting skin integrity.5 The human skin, and mainly the upper layer of the epidermis, plays the role of a barrier, but is also one of the first and major targets of air pollutants. Continuous environmental exposure affects skin health, leading to aging, damages, and even skin diseases (such as erythema, edema, hyperplasia, contact dermatitis, atopic dermatitis, psoriasis, and carcinogenesis) if the environmental stressors exceed the defensive capacity of the skin.6 Major air pollutants with effects on the skin include the solar ultraviolet radiation, polycyclic aromatic hydrocarbons, volatile organic compounds, nitrogen oxides, particulate matter (PM), and cigarette smoke.7 PM is a complex mixture of liquid and/or solid inhalable particles suspended in gas derived from dust, soil, and traffic and industry emissions.3 Recent in vitro and epidemiological studies suggest that PM negatively affects human skin and influences the development and the exacerbation of preexistent skin diseases.8,9 Remarkable evidence shows that oxidative stress – namely increased reactive oxygen species (ROS) production – may be a common pathway in cellular responses of human skin to concentrated ambient particles exposure.8 In an in vitro study, Magnani et al8 showed that among the variety of compounds in air pollution, particularly transition metals participated in Fenton-like reaction and stimulated the cells to generate ROS.8 Besides the generation of free radicals (ROS and reactive nitrogen species), other mechanisms by which ambient air pollutants cause adverse effects on skin health include induction of inflammatory cascade and subsequent impairment of skin barrier, activation of the aryl hydrocarbon receptor, and alterations of skin microflora.10

In this light, external application of natural antioxidants may offer protection against the impacts of air pollution, favoring protective mechanisms of healthy skin that counteract oxidative stress. Among natural exogenous antioxidants, polyphenols are plant-based molecules that have antioxidant properties. It is also well known that polyphenols are effective metal chelators11; the polyphenol–metal interactions (particularly with iron) could represent an antioxidant-causing mechanism.12

Besides their antioxidant properties, polyphenols also exert antiinflammatory and antimicrobial activities, which altogether make them promising tools in alleviating skin damages and preventing the development of various skin disorders.13

In a previous in vitro study,14 we evaluated the capability of three naturally occurring standardized extracts rich in polyphenols (Vitis vinifera [grape] seed extract, Camellia sinensis leaf [green tea] extract, Quercus robur [oak] wood/bark extract), both as single agents and as a multicomponent powder (Vitachelox®), to protect skin fibroblast culture against the toxic effect of polluting agents. Even when belonging to the same chemical class of polyphenols, the naturally occurring standardized extracts are characterized by different polyphenols, typically gallates in the green tea extract, leucocyanidins in the grape seed extract, and tannins in the oak wood extract.

Noteworthy, the multicomponent powder showed a synergistic effect, increasing cell viability over 77% (in comparison with the positive control) in fibroblast cell cultures where environmental damage was experimentally induced. In addition, the multicomponent powder protected fibroblasts against the heavy metal-induced oxidative stress, by restoring the total amount of proteins and preserving the cellular components (lipids, proteins, and DNA).

In this in vivo study, the acute clinical application of the test product on healthy volunteers was evaluated by measuring prevention of any metal deposition within the stratum corneum (SC) following a 6-h exposure period in a polluted environment.

Patients and methods

Thirty healthy volunteers (mean age, 42±2 years; all women) living in the Milan greater area (the leading industrial and commercial city in Northern Italy, and one of the largest in Europe; n=15) or in the Beijing area (the capital of China; n=15) were recruited by a board of certified dermatologists enrolled by a third-party institution involved in the collection of data (Complife Group, Garbagnate Milanese, Milan, Italy). No differences between the two groups were disclosed in terms of baseline characteristics or concentration of metal ions (Table S1).

Written informed consent was obtained before baseline assessment, and the Ethical Committee of Complife group approved the study protocol.

According to the study protocol, only pH-7 detergents were used by volunteers to wash face skin during the 2 days prior to the study initiation. In a random manner, 2 mg/cm2 of the multicomponent powder and of the placebo cream were applied on the hemi-faces of the enrolled participants, respectively. Then, participants were asked to spend six consecutive hours in a polluted area, according to their daily routine. SC samples of both hemi-faces were obtained before and after the exposure, using the tape stripping method (D-Squame®, Cu Derm, Dallas, TX, USA).

The tape skin stripping method is a standardized procedure aimed at obtaining SC samples. In general, this method involves discarding the first strip and bringing the subsequent strips to −80°C prior to transferring five strips in a 50 mL test tube with 20 mL of HCl3N. Then, the test tube is incubated slowly rotating or shaking at 37°C for 12–16 h. Following the incubation period, SC cells are separated by strips, and the solution is analyzed for the detection of heavy metals through atomic absorption spectroscopy.

Data were analyzed by descriptive statistics. The Student t-test was used for intragroup comparisons, with a p value <0.05 considered statistically significant.

Results

No statistically significant variations on the amount of heavy metals were found in the samples of SC cells obtained from the hemi-faces treated with the test product (Table 1). On the contrary, a significantly higher concentration of heavy metals was found in the SC cells samples of the hemi-faces treated with the placebo cream (Table 1). In detail, as illustrated in Figure 1, the following increases in heavy metals concentrations were detected: 95.5% increase in the concentration of chrome (Cr; p<0.001), 130.2% increase in the concentration of iron (Fe; p<0.001), 83.9% increase in the concentration of nickel (Ni; p<0.001), and 142.6% increase in the concentration of zinc (Zn; p<0.001). No differences between Milan and Beijing subgroups were reported (data not shown).

Table 1 Amount of heavy metals found in SC cells samples with the multicomponent powder or placebo

Note: Data are provided as mean (SE).

Abbreviations: Cr, chrome; Fe, iron; Ni, nickel; SC, stratum corneum; Zn, zinc.

Figure 1 Variation (%) in the concentration of heavy metals in SC cells samples. *p<0.001.

Abbreviations: Cr, chrome; Fe, iron; Ni, nickel; SC, stratum corneum; Zn, zinc.

Discussion

The skin is the single largest organ of the human body that provides protection from mechanical impacts and pressure, variations in temperature, microorganisms, radiation, and chemicals. However, the protective ability of the skin is not unlimited, and problems arise when an abnormal exposure to environmental stressors exceeds the skin’s normal defensive potential.14,15 Among all endogenous and exogenous factors that can affect skin health, particularly PM promotes skin tissue damages and plays a role in the pathogenesis of skin diseases.7

In this study, the clinical application of a polyphenol- rich multicomponent powder resulted in a significantly lower metal deposition within the SC of the face skin of 30 healthy volunteers from two polluted areas (Milan and Beijing). Although with some limitations (e.g., low number of participants and lack of some other testing procedures such as patch test), the results from this in vivo study validate and extend to in vitro findings in humans indicating that the polyphenol-rich multicomponent powder protects fibroblast cell cultures against the toxic effect of heavy metals, preserving cell viability, protein synthesis, and the structure of cellular components such as lipids, proteins, and DNA.

The effectiveness of the multicomponent powder in protecting skin cells against air pollution relies on a broad spectrum of well-recognized, pharmacological and therapeutic properties possessed by each single active ingredient, namely grape seed extract, green tea extract, and oak wood extract. In particular, grape seed extract contains several active compounds including flavonoids, polyphenols, anthocyanins, proanthocyanidins, procyanidines, and the stilbene derivative resveratrol that exert antioxidative, antiinflammatory, and antimicrobial activities, thus protecting from the oxidant action of metals.16 Moreover, in experimental studies green tea extracts prevented iron accumulation.17 In addition, grape seed proanthocyanidins significantly inhibited UV-induced skin tumor development as well as suppression of immune system in in vitro and in vivo studies.18 Regarding the antioxidant properties of the green tea extract, these are mainly due to the catechin epigallocatechin-3-gallate – a biologically active polyphenolic compound of green tea that has both direct and indirect antioxidant properties at the cellular level, including scavenging of free radicals, inhibition of ROS-generating enzymes, and reduction of inflammatory cytokines, and above all, chelation of metal ions.19,20 Lastly, results from a recently published in vitro study21 showed that the methanol extracts of Q. robur (oak) bark extract have high radical scavenging capacity, elastase, collagenase, tyrosinase inhibitory activities, and antibacterial activity against Staphylococcus aureus.

Conclusion

The findings of our study indicate that the multicomponent powder allows the prevention of any metal deposition within the SC following exposure in a polluted environment, suggesting that it could play an effective role in counteracting skin damages induced by air pollution.

Disclosure

ST, MM, and GM are employees of Indena S.p.A. LG is a consultant of Indena S.p.A. The authors report no other conflicts of interest in this work.

References

1.

World Health Organisation (WHO). Global Health Risks: Mortality and Burden of Diseases Attributable to Selected Major Risks. Geneva: WHO; 2009. Available from: http://www.who.int/healthinfo/global_burden_disease/GlobalHealthRisks_report_full.pdf. Accessed February 4, 2018.

2.

World Health Organisation (WHO). Air Quality and Health. Geneva: WHO (WHO Fact Sheet No. 313); 2008. Available from: http://www.who.int/mediacentre/factsheets/fs313/en/index.html. Accessed February 4, 2018.

3.

World Health Organisation (WHO). Quantifying Environmental Health Impacts. Geneva: WHO; 2010. Available from: http://www.who.int/quantifying_ehimpacts/en/. Accessed February 4, 2018.

4.

World Health Organisation (WHO). Health Aspects of Air Pollution: Results from the WHO Project “Systematic Review of Health Aspects of Air Pollution in Europe”. Copenhagen: World Health Organization Regional Office for Europe; 2004. http://www.euro.who.int/document/E83080.pdf. Accessed February 4, 2018.

5.

Krutmann J, Liu W, Li L, et al. Pollution and skin: from epidemiological and mechanistic studies to clinical implications. J Dermatol Sci. 2014;76(3):163–168.

6.

Baroni A, Buommino E, De Gregorio V, Ruocco E, Ruocco V, Wolf R. Structure and function of the epidermis related to barrier properties. Clin Dermatol. 2012;30(3):257–262.

7.

Drakaki E, Dessiniotian C, Antoniou CV. Air pollution and the skin. Front Environ Sci. 2014;2(11):1–6.

8.

Magnani ND, Muresan XM, Belmonte G, et al. Skin damage mechanisms related to airborne particulate matter exposure. Toxicol Sci. 2016;149(1):227–236.

9.

Kim KE, Cho D, Park HJ. Air pollution and skin diseases: adverse effects of airborne particulate matter on various skin diseases. Life Sci. 2016;152:126–134.

10.

Mancebo SE, Wang SQ. Recognizing the impact of ambient air pollution on skin health. J Eur Acad Dermatol Venereol. 2015;29(12):2326–2332.

11.

Hider RC, Liu ZD, Khodr HH. Metal chelation of polyphenols. Methods Enzymol. 2001;335:190–203.

12.

Perron NR, Brumaghim JL. A review of the antioxidant mechanisms of polyphenol compounds related to iron binding. Cell Biochem Biophys. 2009;53(2):75–100.

13.

Działo M, Mierziak J, Korzun U, Preisner M, Szopa J, Kulma A. The potential of plant phenolics in prevention and therapy of skin disorders. Int J Mol Sci. 2016;17(2):160.

14.

Giacomelli L, Togni S, Meneghin M, et al. The multi-component powder (Vitachelox) rich in polyphenols protects skin cells against the toxic effects of polluting agents. Esp Dermatol. In press 2017.

15.

Valacchi G, Sticozzi C, Pecorelli A, Cervellati F, Cervellati C, Maioli E. Cutaneous responses to environmental stressors. Ann N Y Acad Sci. 2012;1271:75–81.

16.

Nassiri-Asl M, Hosseinzadeh H. Review of the pharmacological effects of Vitis vinifera (Grape) and its bioactive constituents: an update. Phytother Res. 2016;30(9):1392–1403.

17.

Saewong T, Ounjaijean S, Mundee Y, et al. Effects of green tea on iron accumulation and oxidative stress in livers of iron-challenged thalassemic mice. Med Chem. 2010;6(2):57–64.

18.

Katiyar SK. Proanthocyanidins from grape seeds inhibit UV-radiation-induced immune suppression in mice: detection and analysis of molecular and cellular targets. Photochem Photobiol. 2015;91(1):156–162.

19.

Lorenz M. Cellular targets for the beneficial actions of tea polyphenols. Am J Clin Nutr. 2013;98(6 Suppl):1642S–1650S.

20.

Zink A, Traidl-Hoffmann C. Green tea in dermatology-myths and facts. J Dtsch Dermatol Ges. 2015;13(8):768–775.

21.

Hubert J, Angelis A, Aligiannis N, et al. In vitro dermo-cosmetic evaluation of bark extracts from common temperate trees. Planta Med. 2016;82(15):1351–1358.

Supplementary material

Table S1 Baseline characteristics and concentration of metal ions in the Milan subgroup (n=15) and in the Beijing subgroup (n=15)

Notes: No differences were reported between the two subgroups in any parameter. Data are means (SE) or numbers (%).

Creative Commons License © 2018 The Author(s). This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License. By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.