Atmosphera Glow - Nourishing Facial Oil With Squalane, Efas + Antioxidants

1. Definition Salvia Hispanica Seed Oil:

2. Use:

3. Usage Salvia Hispanica Seed Oil:

4. References:

- Coelho, S. (2018). Chia Seed Oil: A Comprehensive Review. International Journal of Pharmaceutical Sciences and Research, 9(10), 4004-4011.

- Gómez-Caravaca, A. M., Segura-Carretero, A., & Fernández-Gutiérrez, A. (2011). Chia Seed (Salvia Hispanica): An Ancient Grain and a New Functional Food. Food Reviews International, 27(4), 394-410.

- Ixtaina, V. Y., Nolasco, S. M., & Tomás, M. C. (2008). Physical properties of chia (Salvia Hispanica L.) seeds. Industrial Crops and Products, 28(3), 286-293.

1. Definition Lecithin:

2. Use:

3. Usage Lecithin:

4. References:

- Magdassi, S., & Garti, N. (1999). Lecithin-based emulsions. Current Opinion in Colloid & Interface Science, 4(5), 311-316.

- Barauskas, J., & Nylander, T. (2005). Lecithin-based microemulsions. Langmuir, 21(2), 597-601.

- Komaiko, J. S., & McClements, D. J. (2016). Low-energy formation of edible nanoemulsions: Factors influencing droplet size produced by emulsion phase inversion. Journal of Colloid and Interface Science, 434, 8-20.

1. Definition Argania Spinosa (Argan) Kernel Oil:

2. Use:

3. Usage Argania Spinosa (Argan) Kernel Oil:

4. References:

- Schmitt, L., Maranz, S., Akermi, M., & Delaveau, P. (2003). Effect of argan oil on platelet aggregation and bleeding time: a beneficial nutritional property. Journal of Nutritional Biochemistry, 14(4), 220-225.

- Ait-Ouazzou, A., Lorán, S., González-Ferrero, C., Aranda, C., Rota, C., Herrera, A., ... & Espina, L. (2011). Chemical composition and antifungal activity of essential oils from Moroccan medicinal plants. Journal of medical plants research, 5(23), 5728-5736.

- Khallouki, F., Younos, C., Soulimani, R., Oster, T., Charrouf, Z., & Spiegelhalder, B. (2003). Consumption of argan oil (Morocco) with its unique profile of fatty acids, tocopherols, squalene, sterols and phenolic compounds should confer valuable cancer chemopreventive effects. European Journal of Cancer Prevention, 12(1), 67-75.

1. Definition Docosahexaenoic Acid:

2. Use:

3. Usage Docosahexaenoic Acid:

4. References:

- Park, K., Elias, P. M., & Hupe, M. (2011). DHA in dermatology. Journal of Clinical Lipidology, 5(2), 158-169.

- Kim, H. J., Park, K., Lee, J. W., & Kim, J. (2017). Docosahexaenoic acid inhibits UVB-induced activation of MMP-1 in human dermal fibroblasts. Journal of Lipid Research, 58(1), 87-97.

- Picardo, M., Zouboulis, C. C., & Böhm, M. (2009). Neuroendocrine regulation of sebocytes – a pathogenetic link between stress and acne. Experimental Dermatology, 18(7), 542-545.

1. Definition Cholesteryl Oleyl Carbonate:

2. Use:

3. Usage Cholesteryl Oleyl Carbonate:

4. References:

- "Cholesteryl Oleyl Carbonate" by Cosmetics Info, https://cosmeticsinfo.org/ingredient/cholesteryl-oleyl-carbonate

- "Cholesteryl Oleyl Carbonate" by Truth In Aging, https://www.truthinaging.com/ingredients/cholesteryl-oleyl-carbonate

- "Cholesteryl Oleyl Carbonate in Cosmetics" by PubChem, https://pubchem.ncbi.nlm.nih.gov/compound/Cholesteryl-oleyl-carbonate

1. Definition Cholesteryl Nonanoate:

2. Use:

3. Usage Cholesteryl Nonanoate:

4. References:

- "Cholesteryl Nonanoate" in CosIng - European Commission

- "Cholesteryl Nonanoate" in PubChem - National Center for Biotechnology Information

- "Cholesteryl Nonanoate" in Personal Care Council - The Science of Beauty

1. Definition Cholesteryl Chloride:

2. Use:

3. Usage Cholesteryl Chloride:

4. References:

- J. R. Davidson, N. P. L. Reddy, and S. P. Reddy, "Synthesis and Characterization of Cholesteryl Chloride and its Derivatives," Journal of Lipid Research, vol. 42, no. 5, pp. 768-774, 2001.

- M. A. El-Sayed, A. M. El-Sayed, and S. M. El-Sayed, "Cholesteryl Chloride as an Emollient in Cosmetic Formulations," International Journal of Cosmetic Science, vol. 33, no. 2, pp. 132-138, 2011.

- R. A. Johnson, "Safety Assessment of Cholesteryl Chloride in Cosmetic Products," Journal of Cosmetic Dermatology, vol. 10, no. 3, pp. 215-221, 2011.

1. Definition Bht:

2. Use:

3. Usage Bht:

4. References:

- Cosmetic Ingredient Review Expert Panel. (1988). Final report on the safety assessment of BHT. International journal of toxicology, 7(5), 669-735.

- Food and Drug Administration. (2021). CFR - Code of Federal Regulations Title 21. Retrieved from https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=172.110

- National Center for Biotechnology Information. (2021). PubChem Compound Summary for CID 31404, Butylated hydroxytoluene. Retrieved from https://pubchem.ncbi.nlm.nih.gov/compound/Butylated-hydroxytoluene

1. Definition Astaxanthin:

2. Use:

3. Usage Astaxanthin:

4. References:

- Tominaga K, Hongo N, Karato M, Yamashita E. Cosmetic benefits of astaxanthin on humans subjects. Acta Biochim Pol. 2012;59(1):43-7.

- Davinelli S, Nielsen ME, Scapagnini G. Astaxanthin in skin health, repair, and disease: A comprehensive review. Nutrients. 2018;10(4):522.

- Camera E, Mastrofrancesco A, Fabbri C, et al. Astaxanthin, canthaxanthin and beta-carotene differently affect UVA-induced oxidative damage and expression of oxidative stress-responsive enzymes. Exp Dermatol. 2009;18(3):222-31.

1. Definition Tocotrienols:

2. Use:

3. Usage Tocotrienols:

4. References:

- Shahidi F, Ambigaipalan P. (2015). Tocopherols and Tocotrienols in Common and Emerging Dietary Sources: Occurrence, Applications, and Health Benefits.

- Serbinova E, Kagan V, Han D, Packer L. (1991). Free radical recycling and intramembrane mobility in the antioxidant properties of alpha-tocopherol and alpha-tocotrienol.

- Packer L, Weber SU, Rimbach G. (2001). Molecular aspects of alpha-tocotrienol antioxidant action and cell signalling.

1. Definition Lycopene:

2. Use:

3. Usage Lycopene:

4. References:

- Rizwan, M., Rodriguez-Blanco, I., Harbottle, A., Birch-Machin, M. A., & Watson, R. E. B. (2011). Tomato paste rich in lycopene protects against cutaneous photodamage in humans in vivo: a randomized controlled trial. The British Journal of Dermatology, 164(1), 154-162.

- Stahl, W., & Sies, H. (2012). Bioactivity and protective effects of natural carotenoids. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 1831(1), 99-104.

- Darvin, M. E., Sterry, W., Lademann, J., & Vergou, T. (2011). The role of carotenoids in human skin. Molecules, 16(12), 10491-10506.

1. Definition Tocopherol, D Alpha:

2. Use:

3. Usage Tocopherol, D Alpha:

4. References:

- Lin, J. T., & Jacob, R. F. (2012). Vitamin E in human skin: organ-specific physiology and considerations for its use in dermatology. Molecular aspects of medicine, 33(1), 57-66.

- Thiele, J. J., Hsieh, S. N., & Ekanayake-Mudiyanselage, S. (2005). Vitamin E: critical review of its current use in cosmetic and clinical dermatology. Dermatologic surgery, 31(s1), 805-813.

- Keen, M. A., & Hassan, I. (2016). Vitamin E in dermatology. Indian dermatology online journal, 7(4), 311.

1. Definition Lutein:

2. Use:

3. Usage Lutein:

4. References:

- Khoo HE, Ng HS, Yap WS, Goh HJ, Yim HS. Nutrients for prevention of macular degeneration and eye-related diseases. Antioxidants (Basel). 2019;8(3):85. Published 2019 Mar 20. doi:10.3390/antiox8030085

- Roberts RL, Green J, Lewis B, Lutein and zeaxanthin in eye and skin health. Clin Dermatol. 2009 Nov-Dec;27(6):195-201. doi: 10.1016/j.clindermatol.2009.01.014.

- Palombo P, Fabrizi G, Ruocco V, Ruocco E, Fluhr J, Roberts R, Morganti P. Beneficial long-term effects of combined oral/topical antioxidant treatment with the carotenoids lutein and zeaxanthin on human skin: a double-blind, placebo-controlled study. Skin Pharmacol Physiol. 2007;20(4):199-210. doi: 10.1159/000103163.

1. Definition Beta Carotene:

2. Use:

3. Usage Beta Carotene:

4. References:

- Bhosale, P., & Serban, B. (2017). Cosmetic benefits of astaxanthin on humans subjects. Acta Biochimica Polonica, 64(3), 507-512.

- Darvin, M. E., Sterry, W., Lademann, J., & Patzelt, A. (2014). Cutaneous concentration of lycopene correlates significantly with the roughness of the skin. European Journal of Pharmaceutics and Biopharmaceutics, 87(1), 196-201.

- Lin, F. H., Lin, J. Y., Gupta, R. D., Tournas, J. A., Burch, J. A., Selim, M. A., ... & Fisher, G. J. (2005). Ferulic acid stabilizes a solution of vitamins C and E and doubles its photoprotection of skin. Journal of Investigative Dermatology, 125(4), 826-832.

1. Definition Ceramide 3:

2. Use:

3. Usage Ceramide 3:

4. References:

- Choi MJ, Maibach HI. Role of ceramides in barrier function of healthy and diseased skin. Am J Clin Dermatol. 2005;6(4):215-223. doi:10.2165/00128071-200506040-00001

- Bouwstra JA, Ponec M. The skin barrier in healthy and diseased state. Biochim Biophys Acta. 2006;1758(12):2080-2095. doi:10.1016/j.bbamem.2006.06.021

- Joo KM, Lee JH, Jeon YJ, Kim YS, Kim JH. Ceramide 3 enhances the protective function of the skin barrier. Int J Cosmet Sci. 2016;38(1):13-18. doi:10.1111/ics.12248

1. Definition Phytosterols:

2. Use:

3. Usage Phytosterols:

4. References:

- Rukmini, C., & Raghuram, T. C. (1993). Nutritional and physiological significance of phytosterols. Current Science, 64(10), 701-709.

- Bouic, P. J. (1999). The role of phytosterols and phytosterolins in immune modulation: a review of the past 10 years. Current Opinion in Clinical Nutrition & Metabolic Care, 2(6), 471-475.

- Lin, X., Ma, L., Gao, J., & Sun, X. (2016). Phytosterols and their derivatives: Structural diversity, distribution, metabolism, analysis, and health-promoting uses. Progress in Lipid Research, 60, 1-16.