Applications for Marine Resources in Cosmetics
Abstract
:1. Introduction
2. Active Ingredients for Moisturizing Care
3. Active Ingredients to Prevent Skin Aging
4. Active Ingredients for Topical Photoprotection
4.1. Mycosporine-Like Amino Acids
4.2. Scytonemin
5. Active Ingredients with Skin Whitening Properties
6. Marine Resources as a Source of Excipients and Additives for Cosmetics
6.1. Preservatives
6.2. Essential Oil
6.3. Antioxidant
6.4. Dyes
7. Conclusions
Conflicts of Interest
References
- Couteau, C.; Coiffard, L. La Formulation Cosmétique à L’usage des Professionnels et des Amateurs; Le Moniteur: Paris, France, 2014. [Google Scholar]
- Couteau, C.; Coiffard, L. Seaweed Application in Cosmetics. In Seaweed in Health and Disease Prevention; Academic Press: Cambridge, MA, USA, 2016. [Google Scholar]
- Mora, C.; Tittensor, D.P.; Adl, S.; Simpson, A.G.; Worm, B. How many species are there on Earth and in the ocean? PLoS Biol. 2011, 9, e1001127. [Google Scholar] [CrossRef] [PubMed]
- Corinaldesi, C.; Barone, G.; Marcellini, F.; Dell’Anno, A.; Danovaro, R. Marine Microbial-Derived Molecules and Their Potential Use in Cosmeceutical and Cosmetic Products. Mar. Drugs 2017, 15. [Google Scholar] [CrossRef] [PubMed]
- Danovaro, R.; Snelgrove, P.V.; Tyler, P. Challenging the paradigms of deep-sea ecology. Trends Ecol. Evolut. 2014, 29, 465–475. [Google Scholar] [CrossRef] [PubMed]
- Panno, L.; Bruno, M.; Voyron, S.; Anastasi, A.; Gnavi, G.; Miserere, L.; Varese, G.C. Diversity, ecological role and potential biotechnological applications of marine fungi associated to the seagrass Posidonia oceanica. New Biotechnol. 2013, 30, 685–694. [Google Scholar] [CrossRef] [PubMed]
- Blunt, J.W.; Copp, B.R.; Keyzers, R.A.; Munro, M.H.; Prinsep, M.R. Marine natural products. Nat. Prod. Rep. 2016, 33, 382–431. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Li, Y.; Horsman, M.; Wang, B.; Wu, N.; Lan, C.Q. Effects of nitrogen sources on cell growth and lipid accumulation of green alga Neochloris oleoabundans. Appl. Microbiol. Biotechnol. 2008, 81, 629–636. [Google Scholar] [CrossRef] [PubMed]
- Li, Y.; Horsman, M.; Wu, N.; Lan, C.Q.; Dubois-Calero, N. Biofuels from microalgae. Biotechnol. Prog. 2008, 24, 815–820. [Google Scholar] [CrossRef] [PubMed]
- Carballo-Cárdenas, E.C.; Tuan, P.M.; Janssen, M.; Wijffels, R.H. Vitamin E (alpha-tocopherol) production by the marine microalgae Dunaliella tertiolecta and Tetraselmis suecica in batch cultivation. Biomol. Eng. 2003, 20, 139–147. [Google Scholar] [CrossRef]
- Li, H.-B.; Chen, F. Preparative isolation and purification of astaxanthin from the microalga Chlorococcum sp. by high-speed counter-current chromatography. J. Chromatogr. A 2001, 925, 133–137. [Google Scholar] [CrossRef]
- Lorenz, R.T.; Cysewski, G.R. Commercial potential for Haematococcus microalgae as a natural source of astaxanthin. Trends Biotechnol. 2000, 18, 160–167. [Google Scholar] [CrossRef]
- Cuellar-Bermudez, S.P.; Aguilar-Hernandez, I.; Cardenas-Chavez, D.L.; Ornelas-Soto, N.; Romero-Ogawa, M.A.; Parra-Saldivar, R. Extraction and purification of high-value metabolites from microalgae: Essential lipids, astaxanthin and phycobiliproteins. Microb. Biotechnol. 2015, 8, 190–209. [Google Scholar] [CrossRef] [PubMed]
- Imhoff, J.F.; Labes, A.; Wiese, J. Bio-mining the microbial treasures of the ocean: New natural products. Biotechnol. Adv. 2011, 29, 468–482. [Google Scholar] [CrossRef] [PubMed]
- Jin, L.; Quan, C.; Hou, X.; Fan, S. Potential Pharmacological Resources: Natural Bioactive Compounds from Marine-Derived Fungi. Mar. Drugs 2016, 14. [Google Scholar] [CrossRef] [PubMed]
- Ziboh, V.A.; Chapkin, R.S. Biologic significance of polyunsaturated fatty acids in the skin. Arch. Dermatol. 1987, 123, 1686–1690. [Google Scholar] [CrossRef]
- Press, M.; Hartop, P.J.; Prottey, C. Correction of essential fatty-acid deficiency in man by the cutaneous application of sunflower-seed oil. Lancet 1974, 1, 597–598. [Google Scholar] [CrossRef]
- Bellou, S.; Aggelis, G. Biochemical activities in Chlorella sp. and Nannochloropsis salina during lipid and sugar synthesis in a lab-scale open pond simulating reactor. J. Biotechnol. 2012, 164, 318–329. [Google Scholar] [CrossRef] [PubMed]
- Cardozo, K.H.; Guaratini, T.; Barros, M.P.; Falcao, V.R.; Tonon, A.P.; Lopes, N.P.; Campos, S.; Torres, M.A.; Souza, A.O.; Colepicolo, P.; et al. Metabolites from algae with economical impact. Comp. Biochem. Physiol. Toxicol. Pharmacol. CBP 2007, 146, 60–78. [Google Scholar] [CrossRef] [PubMed]
- Xhauflaire-Uhoda, E.; Fontaine, K.; Pierard, G.E. Kinetics of moisturizing and firming effects of cosmetic formulations. Int. J. Cosmetic Sci. 2008, 30, 131–138. [Google Scholar] [CrossRef] [PubMed]
- Venkatesan, J.; Anil, S.; Kim, S.K.; Shim, M.S. Marine Fish Proteins and Peptides for Cosmeceuticals: A Review. Mar. Drugs 2017, 15. [Google Scholar] [CrossRef] [PubMed]
- Jimbo, N.; Kawada, C.; Nomura, Y. Optimization of dose of collagen hydrolysate to prevent UVB-irradiated skin damage. Biosci. Biotechnol. Biochem. 2016, 80, 356–359. [Google Scholar] [CrossRef] [PubMed]
- Bownik, A.; Stepniewska, Z. Ectoine as a promising protective agent in humans and animals. Arh. Hig. Rada Toksikol. 2016, 67, 260–265. [Google Scholar] [CrossRef] [PubMed]
- Galinski, E.A.; Pfeiffer, H.-P.; Truper, H.G. 1,4,5,6-Tetrahydro-2-methyl-4-pyrimidinecarboxylic acid. A novel cyclic amino acid from halophilic phototrophic bacteria of the genus Ectothiorhodospira. Eur. J. Biochem. 1985, 149, 135–139. [Google Scholar] [CrossRef] [PubMed]
- Smiatek, J.; Harishchandra, R.K.; Rubner, O.; Galla, H.J.; Heuer, A. Properties of compatible solutes in aqueous solution. Biophys. Chem. 2012, 160, 62–68. [Google Scholar] [CrossRef] [PubMed]
- Heinrich, U.; Garbe, B.; Tronnier, H. In vivo assessment of Ectoin: A randomized, vehicle-controlled clinical trial. Skin Pharmacol. Physiol. 2007, 20, 211–218. [Google Scholar] [CrossRef] [PubMed]
- Zaccai, G.; Bagyan, I.; Combet, J.; Cuello, G.J.; Deme, B.; Fichou, Y.; Gallat, F.X.; Galvan Josa, V.M.; von Gronau, S.; Haertlein, M.; et al. Neutrons describe ectoine effects on water H-bonding and hydration around a soluble protein and a cell membrane. Sci. Rep. 2016, 6, 31434. [Google Scholar] [CrossRef] [PubMed]
- Marini, A.; Reinelt, K.; Krutmann, J.; Bilstein, A. Ectoine-containing cream in the treatment of mild to moderate atopic dermatitis: A randomised, comparator-controlled, intra-individual double-blind, multi-center trial. Skin Pharmacol. Physiol. 2014, 27, 57–65. [Google Scholar] [CrossRef] [PubMed]
- Graf, R.; Anzali, S.; Buenger, J.; Pfluecker, F.; Driller, H. The multifunctional role of ectoine as a natural cell protectant. Clin. Dermatol. 2008, 26, 326–333. [Google Scholar] [CrossRef] [PubMed]
- Alvarez-Rivera, G.; Llompart, M.; Garcia-Jares, C.; Lores, M. Identification of unwanted photoproducts of cosmetic preservatives in personal care products under ultraviolet-light using solid-phase microextraction and micro-matrix solid-phase dispersion. J. Chromatogr. A 2015, 1390, 1–12. [Google Scholar] [CrossRef] [PubMed]
- De Jesus Raposo, M.F.; de Morais, R.M.; de Morais, A.M. Health applications of bioactive compounds from marine microalgae. Life Sci. 2013, 93, 479–486. [Google Scholar] [CrossRef] [PubMed]
- Higuera-Ciapara, I.; Felix-Valenzuela, L.; Goycoolea, F.M. Astaxanthin: A review of its chemistry and applications. Crit. Rev. Food Sci. Nutr. 2006, 46, 185–196. [Google Scholar] [CrossRef] [PubMed]
- Gammone, M.A.; Riccioni, G.; D’Orazio, N. Marine Carotenoids against Oxidative Stress: Effects on Human Health. Mar. Drugs 2015, 13, 6226–6246. [Google Scholar] [CrossRef] [PubMed]
- Terao, J. Antioxidant activity of b-carotene-related carotenoids in solution. Lipids 1989, 24, 659–661. [Google Scholar] [CrossRef] [PubMed]
- Tripathi, U.; Sarada, R.; Rao, S.R.; Ravishankar, G.A. Production of astaxanthin in Haematococcus pluvialis cultured in various media. Bioresour. Technol. 1999, 68, 197–199. [Google Scholar] [CrossRef]
- Olaizola, M.; Huntley, M.E. Recent advances in commercial production of astaxanthin from microalgae. In Recent Advances in Marine Biotechnology; Fingerman, M., Nagabhushaman, R., Eds.; Science Publishers: Enfield, NH, USA, 2003; Volume 9, pp. 143–164. [Google Scholar]
- Wan, M.; Hou, D.; Li, Y.; Fan, J.; Huang, J.; Liang, S.; Wang, W.; Pan, R.; Wang, J.; Li, S. The effective photoinduction of Haematococcus pluvialis for accumulating astaxanthin with attached cultivation. Bioresour. Technol. 2014, 163, 26–32. [Google Scholar] [CrossRef] [PubMed]
- Shindo, K.; Kikuta, K.; Suzuki, A.; Katsuta, A.; Kasai, H.; Yasumoto-Hirose, M.; Matsuo, Y.; Misawa, N.; Takaichi, S. Rare carotenoids, (3R)-saproxanthin and (3R,2′S)-myxol, isolated from novel marine bacteria (Flavobacteriaceae) and their antioxidative activities. Appl. Microbiol. Biotechnol. 2007, 74, 1350–1357. [Google Scholar] [CrossRef] [PubMed]
- Poli, A.; Anzelmo, G.; Nicolaus, B. Bacterial exopolysaccharides from extreme marine habitats: Production, characterization and biological activities. Mar. Drugs 2010, 8, 1779–1802. [Google Scholar] [CrossRef] [PubMed]
- Le Costaouec, T.; Cerantola, S.; Ropartz, D.; Ratiskol, J.; Sinquin, C.; Colliec-Jouault, S.; Boisset, C. Structural data on a bacterial exopolysaccharide produced by a deep-sea Alteromonas macleodii strain. Carbohydr. Polym. 2012, 90, 49–59. [Google Scholar] [CrossRef] [PubMed]
- Courtois, A.; Berthou, C.; Guezennec, J.; Boisset, C.; Bordron, A. Exopolysaccharides isolated from hydrothermal vent bacteria can modulate the complement system. PLoS ONE 2014, 9, e94965. [Google Scholar] [CrossRef] [PubMed]
- Martins, A.; Vieira, H.; Gaspar, H.; Santos, S. Marketed marine natural products in the pharmaceutical and cosmeceutical industries: Tips for success. Mar. Drugs 2014, 12, 1066–1101. [Google Scholar] [CrossRef] [PubMed]
- Bloch, J.F.; Tardieu-Guigues, E. Marine biotechnologies and synthetic biology, new issues for a fair and equitable profit-sharing commercial use. Mar. Genom. 2014, 17, 79–83. [Google Scholar] [CrossRef] [PubMed]
- Wang, H.M.; Chen, C.C.; Huynh, P.; Chang, J.S. Exploring the potential of using algae in cosmetics. Bioresour. Technol. 2015, 184, 355–362. [Google Scholar] [CrossRef] [PubMed]
- Price, R.D.; Berry, M.G.; Navsaria, H.A. Hyaluronic acid: The scientific and clinical evidence. J. Plast. Reconstr. Aesthet. Surg. 2007, 60, 1110–1119. [Google Scholar] [CrossRef] [PubMed]
- McCullough, J.L.; Kelly, K.M. Prevention and treatment of skin aging. Ann. N. Y. Acad. Sci. 2006, 1067, 323–331. [Google Scholar] [CrossRef] [PubMed]
- Kim, M.M.; Ta, Q.V.; Mendis, E.; Rajapakse, N.; Jung, W.K.; Byun, H.G.; Jeon, Y.J.; Kim, S.K. Phlorotannins in Ecklonia cava extract inhibit matrix metalloproteinase activity. Life Sci. 2006, 79, 1436–1443. [Google Scholar] [CrossRef] [PubMed]
- Sanjeewa, K.K.; Kim, E.A.; Son, K.T.; Jeon, Y.J. Bioactive properties and potentials cosmeceutical applications of phlorotannins isolated from brown seaweeds: A review. J. Photochem. Photobiol. B Biol. 2016, 162, 100–105. [Google Scholar] [CrossRef] [PubMed]
- Varani, J.; Warner, R.L.; Gharaee-Kermani, M.; Phan, S.H.; Kang, S.; Chung, J.H.; Wang, Z.Q.; Datta, S.C.; Fisher, G.J.; Voorhees, J.J. Vitamin A antagonizes decreased cell growth and elevated collagen-degrading matrix metalloproteinases and stimulates collagen accumulation in naturally aged human skin. J. Investig. Dermatol. 2000, 114, 480–486. [Google Scholar] [CrossRef] [PubMed]
- Sim, G.-S.; Lee, B.-C.; Cho, H.S.; Lee, J.W.; Kim, J.-H.; Lee, D.-H.; Kim, J.-H.; Pyo, H.-B.; Moon, D.C.; Oh, K.-W.; et al. Structure activity relationship of antioxidative property of flavonoids and inhibitory effect on matrix metalloproteinase activity in UVA-irradiated human dermal fibroblast. Arch. Pharmacal Res. 2007, 30, 290–298. [Google Scholar] [CrossRef]
- Ryu, B.; Qian, Z.J.; Kim, S.K. Purification of a peptide from seahorse, that inhibits TPA-induced MMP, iNOS and COX-2 expression through MAPK and NF-kappaB activation, and induces human osteoblastic and chondrocytic differentiation. Chem. Biol. Interact. 2010, 184, 413–422. [Google Scholar] [CrossRef] [PubMed]
- Ryu, B.; Qian, Z.J.; Kim, S.K. SHP-1, a novel peptide isolated from seahorse inhibits collagen release through the suppression of collagenases 1 and 3, nitric oxide products regulated by NF-kappaB/p38 kinase. Peptides 2010, 31, 79–87. [Google Scholar] [CrossRef] [PubMed]
- Lodemel, J.B.; Egge-Jacobsen, W.; Olsen, R.L. Detection of TIMP-2-like protein in Atlantic cod (Gadus morhua) muscle using two-dimensional real-time reverse zymography. Comp. Biochem. Physiol. Part B Biochem. Mol. Biol. 2004, 139, 253–259. [Google Scholar] [CrossRef] [PubMed]
- Zhang, C.; Kim, S.K. Matrix metalloproteinase inhibitors (MMPIs) from marine natural products: The current situation and future prospects. Mar. Drugs 2009, 7, 71–84. [Google Scholar] [CrossRef] [PubMed]
- Joe, M.-J.; Kim, S.-N.; Choi, H.-Y.; Shin, W.-S.; Park, G.-M.; Kang, D.-W.; Kim, Y.K. The Inhibitory Effects of Eckol and Dieckol from Ecklonia stolonifera on the Expression of Matrix Metalloproteinase-1 in Human Dermal Fibroblasts. Biol. Pharm. Bull. 2006, 29, 1735–1739. [Google Scholar] [CrossRef] [PubMed]
- Zhang, C.; Li, Y.; Shi, X.; Kim, S.-K. Inhibition of the expression on MMP-2, 9 and morphological changes via human fibrosarcoma cell line by 6,6′-bieckol from marine alga Ecklonia cava. BMB Rep. 2010, 43, 62–68. [Google Scholar] [CrossRef] [PubMed]
- Ma’Or, Z.; Yehuda, S.; Voss, W. Skin smoothing effects of Dead Sea minerals: Comparative profilometric evaluation of skin surface. Int. J. Cosmet. Sci. 1997, 19, 105–110. [Google Scholar] [CrossRef] [PubMed]
- Blanco-Davila, F. Beauty and the Body: The Origins of Cosmetics. Plast. Reconstr. Surg. 2000, 105, 1196–1204. [Google Scholar] [CrossRef] [PubMed]
- Kim, S.K. Marine cosmeceuticals. J. Cosmet. Dermatol. 2014, 13, 56–67. [Google Scholar] [CrossRef] [PubMed]
- Momani, K.; El-Hasan, T.; Auaydeh, S.; Al-Nawayseh, K. Heavy Metals Distribution in the Dead Sea Black Mud Jordan. J. Earth Environ. Sci. 2009, 2, 50–59. [Google Scholar]
- Lin, S. Heavy metal removal from water by sorption using surfactant-modified montmorillonite. J. Hazard. Mater. 2002, 92, 315–326. [Google Scholar] [CrossRef]
- Ma’or, Z.; Halicz, L.; Portugal-Cohen, M.; Russo, M.Z.; Robino, F.; Vanhaecke, T.; Rogiers, V. Safety evaluation of traces of nickel and chrome in cosmetics: The case of Dead Sea mud. Regul. Toxicol. Pharmacol. RTP 2015, 73, 797–801. [Google Scholar] [CrossRef] [PubMed]
- Diffey, B.L. Solar UV effect on biological systems. Phys. Med. Biol. 1991, 36, 299–328. [Google Scholar] [CrossRef] [PubMed]
- Rittie, L.; Fisher, G.J. UV-light-induced signal cascades and skin aging. Ageing Res. Rev. 2002, 1, 705–720. [Google Scholar] [CrossRef]
- Young, A.R.; Claveau, J.; Rossi, A.B. Ultraviolet radiation and the skin: Photobiology and sunscreen photoprotection. J. Am. Acad. Dermatol. 2017, 76, S100–S109. [Google Scholar] [CrossRef] [PubMed]
- Carreto, J.I.; Carignan, M.O. Mycosporine-like amino acids: Relevant secondary metabolites. Chemical and ecological aspects. Mar. Drugs 2011, 9, 387–446. [Google Scholar] [CrossRef] [PubMed]
- Gao, Q.; Garcia-Pichel, F. Microbial ultraviolet sunscreens. Nat. Rev. Microbiol. 2011, 9, 791–802. [Google Scholar] [CrossRef] [PubMed]
- Pallela, R.; Na-Young, Y.; Kim, S.K. Anti-photoaging and photoprotective compounds derived from marine organisms. Mar. Drugs 2010, 8, 1189–1202. [Google Scholar] [CrossRef] [PubMed]
- Rastogi, R.P.; Richa; Sinha, R.P.; Singh, S.P.; Hader, D.P. Photoprotective compounds from marine organisms. J. Ind. Microbiol. Biotechnol. 2010, 37, 537–558. [Google Scholar] [CrossRef] [PubMed]
- Sinha, R.P.; Singh, S.P.; Hader, D.P. Database on mycosporines and mycosporine-like amino acids (MAAs) in fungi, cyanobacteria, macroalgae, phytoplankton and animals. J. Photochem. Photobiol. B 2007, 89, 29–35. [Google Scholar] [CrossRef] [PubMed]
- Singh, S.P.; Kumari, S.; Rastogi, R.P.; Singh, K.L.; Sinha, R.P. Mycosporine-like amino acids (MAAs): Chemical structure, biosynthesis and significance as UV-absorbing/screening compounds. Indian J. Exp. Biol. 2008, 46, 7–17. [Google Scholar] [PubMed]
- Siezen, R.J. Microbial sunscreens. Microb. Biotechnol. 2011, 4, 1–7. [Google Scholar] [CrossRef] [PubMed]
- Sinha, R.a.R.P. UV-mediated stress ans its mitigation in Cyanobacteria. Int. J. Plant Anim. Environ. Sci. 2011, 1, 155–166. [Google Scholar]
- Groniger, A.; Sinha, R.P.; Klisch, M.; Hader, D.P. Photoprotective compounds in cyanobacteria, phytoplankton and macroalgae—A database. J. Photochem. Photobiol. B 2000, 58, 115–122. [Google Scholar] [CrossRef]
- Ehling-Schulz, M.; Bilger, W.; Scherer, S. UV-B-induced synthesis of photoprotective pigments and extracellular polysaccharides in the terrestrial cyanobacterium Nostoc commune. J. Bacteriol. 1997, 179, 1940–1945. [Google Scholar] [CrossRef] [PubMed]
- Garcia-Pichel, F.; Castenholz, R.W. Characterization and biological implications of scytonemin, a cyanobacterial sheath pigment. J. Phycol. 1991, 395–409. [Google Scholar] [CrossRef]
- Sorrels, C.M.; Proteau, P.J.; Gerwick, W.H. Organization, evolution, and expression analysis of the biosynthetic gene cluster for scytonemin, a cyanobacterial UV-absorbing pigment. Appl. Environ. Microbiol. 2009, 75, 4861–4869. [Google Scholar] [CrossRef] [PubMed]
- Rastogi, R.P.; Sonani, R.R.; Madamwar, D. Cyanobacterial Sunscreen Scytonemin: Role in Photoprotection and Biomedical Research. Appl. Biochem. Biotechnol. 2015, 176, 1551–1563. [Google Scholar] [CrossRef] [PubMed]
- Dillon, J.G.; Tatsumi, C.M.; Tandingan, P.G.; Castenholz, R.W. Effect of environmental factors on the synthesis of scytonemin, a UV-screening pigment, in a cyanobacterium (Chroococcidiopsis sp.). Arch. Microbiol. 2002, 177, 322–331. [Google Scholar] [CrossRef] [PubMed]
- Proteau, P.J.; Gerwick, W.H.; Garcia-Pichel, F.; Castenholz, R. The structure of scytonemin, an ultraviolet sunscreen pigment from the sheats of cyanobacteria. Experientia 1993, 49, 825–829. [Google Scholar] [CrossRef] [PubMed]
- Rastogi, R.P.; Incharoensakdi, A. Characterization of UV-screening compounds, mycosporine-like amino acids, and scytonemin in the cyanobacterium Lyngbya sp. CU2555. FEMS Microbiol. Ecol. 2014, 87, 244–256. [Google Scholar] [CrossRef] [PubMed]
- Rastogi, R.P.; Sinha, R.P.; Incharoensakdi, A. Partial characterization, UV-induction and photoprotective function of sunscreen pigment, scytonemin from Rivularia sp. HKAR-4. Chemosphere 2013, 93, 1874–1878. [Google Scholar] [CrossRef] [PubMed]
- Pillaiyar, T.; Manickam, M.; Namasivayam, V. Skin whitening agents: Medicinal chemistry perspective of tyrosinase inhibitors. J. Enzyme Inhib. Med. Chem. 2017, 32, 403–425. [Google Scholar] [CrossRef] [PubMed]
- Burger, P.; Landreau, A.; Azoulay, S.; Michel, T.; Fernandez, X. Skin Whitening Cosmetics: Feedback and Challenges in the Development of Natural Skin Lighteners. Cosmetics 2016, 3, 36. [Google Scholar] [CrossRef]
- Shen, C.-T.; Chen, P.-Y.; Wu, J.-J.; Lee, T.-M.; Hsu, S.-L.; Chang, C.-M.J.; Young, C.-C.; Shieh, C.-J. Purification of algal anti-tyrosinase zeaxanthin from Nannochloropsis oculata using supercritical anti-solvent precipitation. J. Supercrit. Fluids 2011, 55, 955–962. [Google Scholar] [CrossRef]
- Yoon, N.Y.; Eom, T.K.; Kim, M.M.; Kim, S.K. Inhibitory effect of phlorotannins isolated from Ecklonia cava on mushroom tyrosinase activity and melanin formation in mouse B16F10 melanoma cells. J. Agric. Food Chem. 2009, 57, 4124–4129. [Google Scholar] [CrossRef] [PubMed]
- Kang, H.Y.; Yoon, T.J.; Lee, G.J. Whitening effects of marine pseudomonas extract. Ann. Dermatol. 2011, 23, 144–149. [Google Scholar] [CrossRef] [PubMed]
- Deering, R.W.; Chen, J.; Sun, J.; Ma, H.; Dubert, J.; Barja, J.L.; Seeram, N.P.; Wang, H.; Rowley, D.C. N-Acyl Dehydrotyrosines, Tyrosinase Inhibitors from the Marine Bacterium Thalassotalea sp. PP2–459. J. Nat. Prod. 2016, 79, 447–450. [Google Scholar] [CrossRef] [PubMed]
- Ambati, R.R.; Phang, S.M.; Ravi, S.; Aswathanarayana, R.G. Astaxanthin: Sources, extraction, stability, biological activities and its commercial applications—A review. Mar. Drugs 2014, 12, 128–152. [Google Scholar] [CrossRef] [PubMed]
- Dzialo, 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, 160. [Google Scholar] [CrossRef] [PubMed]
- Lopes, A.; Rodrigues, M.J.; Pereira, C.; Oliveira, M.; Barreira, L.; Varela, J.; Trampetti, F.; Custódio, L. Natural products from extreme marine environments: Searching for potential industrial uses within extremophile plants. Ind. Crops Prod. 2016, 94, 299–307. [Google Scholar] [CrossRef]
- Rodriguez-Perez, C.; Quirantes-Pine, R.; Amessis-Ouchemoukh, N.; Madani, K.; Segura-Carretero, A.; Fernandez-Gutierrez, A. A metabolite-profiling approach allows the identification of new compounds from Pistacia lentiscus leaves. J. Pharm. Biomed. Anal. 2013, 77, 167–174. [Google Scholar] [CrossRef] [PubMed]
- Sato, K.; Toriyama, M. Depigmenting effect of catechins. Molecules 2009, 14, 4425–4432. [Google Scholar] [CrossRef] [PubMed]
- Kubo, I.; Chen, Q.-X.; Nihei, K.-I. Molecular design of antibrowning agents: Antioxidative tyrosinase inhibitors. Food Chem. 2003, 81, 241–247. [Google Scholar] [CrossRef]
- Momtaz, S.; Mapunya, B.M.; Houghton, P.J.; Edgerly, C.; Hussein, A.; Naidoo, S.; Lall, N. Tyrosinase inhibition by extracts and constituents of Sideroxylon inerme L. stem bark, used in South Africa for skin lightening. J. Ethnopharmacol. 2008, 119, 507–512. [Google Scholar] [CrossRef] [PubMed]
- Routledge, E.J.; Parker, J.; Odum, J.; Ashby, J.; Sumpter, J.P. Some alkyl hydroxy benzoate preservatives (parabens) are estrogenic. Toxicol. Appl. Pharmacol. 1998, 153, 12–19. [Google Scholar] [CrossRef] [PubMed]
- Darbre, P.D.; Aljarrah, A.; Miller, W.R.; Coldham, N.G.; Sauer, M.J.; Pope, G.S. Concentrations of parabens in human breast tumours. J. Appl. Toxicol. JAT 2004, 24, 5–13. [Google Scholar] [CrossRef] [PubMed]
- Plaza, M.; Santoyo, S.; Jaime, L.; Garcia-Blairsy Reina, G.; Herrero, M.; Senorans, F.J.; Ibanez, E. Screening for bioactive compounds from algae. J. Pharm. Biomed. Anal. 2010, 51, 450–455. [Google Scholar] [CrossRef] [PubMed]
- Srinivasakumar, K.P.; Rajashekhar, M. In vitro Studies on Bactericidal Activity and Sensitivity Pattern of Isolated Marine Microalgae against Selective Human Bacterial Pathogens. Indian J. Sci. Technol. 2009, 2, 16–23. [Google Scholar]
- Friedman, M.; Junja, V.K. Review of Antimicrobial and Antioxidative Activities of Chitosans in Food. J. Food Prot. 2010, 73, 1737–1761. [Google Scholar] [CrossRef] [PubMed]
- Younes, I.; Rinaudo, M. Chitin and chitosan preparation from marine sources. Structure, properties and applications. Mar. Drugs 2015, 13, 1133–1174. [Google Scholar] [CrossRef] [PubMed]
- Tharanathan, R.N.; Kittur, F.S. Chitin--the undisputed biomolecule of great potential. Crit. Rev. Food Sci. Nutr. 2003, 43, 61–87. [Google Scholar] [CrossRef] [PubMed]
- Meot-Duros, L.; Cerantola, S.; Talarmin, H.; Le Meur, C.; Le Floch, G.; Magne, C. New antibacterial and cytotoxic activities of falcarindiol isolated in Crithmum maritimum L. leaf extract. Food Chem. Toxicol. Int. J. Publ. Br. Ind. Biol. Res. Assoc. 2010, 48, 553–557. [Google Scholar] [CrossRef] [PubMed]
- Chi, C.F.; Cao, Z.H.; Wang, B.; Hu, F.Y.; Li, Z.R.; Zhang, B. Antioxidant and functional properties of collagen hydrolysates from Spanish mackerel skin as influenced by average molecular weight. Molecules 2014, 19, 11211–11230. [Google Scholar] [CrossRef] [PubMed]
- Bardan, A.; Nizet, V.; Gallo, R.L. Antimicrobial peptides and the skin. Expert Opin. Biol. Ther. 2004, 4, 543–549. [Google Scholar] [CrossRef] [PubMed]
- Song, R.; Wei, R.B.; Luo, H.Y.; Wang, D.F. Isolation and characterization of an antibacterial peptide fraction from the pepsin hydrolysate of half-fin anchovy (Setipinna taty). Molecules 2012, 17, 2980–2991. [Google Scholar] [CrossRef] [PubMed]
- Ennaas, N.; Hammami, R.; Beaulieu, L.; Fliss, I. Purification and characterization of four antibacterial peptides from protamex hydrolysate of Atlantic mackerel (Scomber scombrus) by-products. Biochem. Biophys. Res. Commun. 2015, 462, 195–200. [Google Scholar] [CrossRef] [PubMed]
- Coiffard, L.; Alliot, A.; Piron-Frenet, M. Seasonal and geographical adaptation of Crithmum maritimum L.: Variations in inorganic content. Ecol. Food Nut. 1992, 28, 261–269. [Google Scholar] [CrossRef]
- Coiffard, L.; Piron-Frenet, M.; Amicel, L. Geographical variations of the constituents of the essential oil of Crithmum maritimum L., Apiaceae. Int. J. Cosmetic Sci. 1993, 15, 15–21. [Google Scholar] [CrossRef]
- Park, P.-J.; Jung, W.-K.; Nam, K.-S.; Shahidi, F.; Kim, S.-K. Purification and characterization of antioxidative peptides from protein hydrolysate of lecithin-free egg yolk. J. Am. Oil Chem. Soc. 2001, 78, 651–656. [Google Scholar] [CrossRef]
- Hettiarachchy, N.S.; Glenn, K.C.; Gnanasambandam, R.; Johnson, M.G. Natural Antioxidant Extract from Fenugreek (Trigonella foenumgraecum) for Ground Beef Patties. J. Food Sci. 1996, 61, 516–519. [Google Scholar] [CrossRef]
- Al-Amoudi, O.A.; Mutawie, H.H.; Patel, A.V.; Blunden, G. Chemical composition and antioxidant activities of Jeddah corniche algae, Saudi Arabia. Saudi J. Biol. Sci. 2009, 16, 23–29. [Google Scholar] [CrossRef] [PubMed]
- Bataille, M. Comment les Organismes Vivants se Protègent-ils du Soleil; Université de Nantes: Nantes, France, 2016. [Google Scholar]
- Kirti, K.; Amita, S.; Priti, S.; Mukesh Kumar, A.; Jyoti, S. Colorful World of Microbes: Carotenoids and Their Applications. Adv. Biol. 2014, 2014, 1–13. [Google Scholar] [CrossRef]
- Morabito, K.; Shapley, N.C.; Steeley, K.G.; Tripathi, A. Review of sunscreen and the emergence of non-conventional absorbers and their applications in ultraviolet protection. Int. J. Cosmetic Sci. 2011, 33, 385–390. [Google Scholar] [CrossRef] [PubMed]
- Vilchez, C.; Forjan, E.; Cuaresma, M.; Bedmar, F.; Garbayo, I.; Vega, J.M. Marine carotenoids: Biological functions and commercial applications. Mar. Drugs 2011, 9, 319–333. [Google Scholar] [CrossRef] [PubMed]
- Mata-Gómez, L.C.; Montañez, J.C.; Méndez-Zavala, A.; Aguilar, C.N. Biotechnological production of carotenoids by yeasts: An overview. Microb. Cell Fact. 2014, 13, 12. [Google Scholar] [CrossRef] [PubMed]
- Suen, Y.L.; Tang, H.; Huang, J.; Chen, F. Enhanced production of fatty acids and astaxanthin in Aurantiochytrium sp. by the expression of Vitreoscilla hemoglobin. J. Agric. Food Chem. 2014, 62, 12392–12398. [Google Scholar] [CrossRef] [PubMed]
- Takaichi, S. Carotenoids in algae: Distributions, biosyntheses and functions. Mar. Drugs 2011, 9, 1101–1118. [Google Scholar] [CrossRef] [PubMed]
- Borowitzka, L.J. β-carotene (provitamin A) production with algae. In Biotechnology of Vitamins, Pigments and Growth Factors; Vandamme, E.J., Ed.; Applied Biotechnology Series; Springer Science & Business Media: Berlin, Germany, 1989; Chapter 2. [Google Scholar]
- Quilodrán, B.; Hinzpeter, I.; Hormazabal, E.; Quiroz, A.; Shene, C. Docosahexaenoic acid (C22:6n−3, DHA) and astaxanthin production by Thraustochytriidae sp. AS4-A1 a native strain with high similitude to Ulkenia sp.: Evaluation of liquid residues from food industry as nutrient sources. Enzyme Microb. Technol. 2010, 47, 24–30. [Google Scholar] [CrossRef]
- Amon, J.P.; French, K.H. Photoresponses of the marine protist Ulkenia sp. zoospores to ambient, artificial and bioluminescent light. Mycologia 2017, 96, 463–469. [Google Scholar] [CrossRef]
- Surget, G.; Stiger-Pouvreau, V.; Le Lann, K.; Kervarec, N.; Couteau, C.; Coiffard, L.J.; Gaillard, F.; Cahier, K.; Guerard, F.; Poupart, N. Structural elucidation, in vitro antioxidant and photoprotective capacities of a purified polyphenolic-enriched fraction from a saltmarsh plant. J. Photochem. Photobiol. B Biol. 2015, 143, 52–60. [Google Scholar] [CrossRef] [PubMed]
- Dai, J.; Mumper, R.J. Plant phenolics: Extraction, analysis and their antioxidant and anticancer properties. Molecules 2010, 15, 7313–7352. [Google Scholar] [CrossRef] [PubMed]
- Aniya, Y.; Miyagi, C.; Nakandakari, A.; Kamiya, S.; Imaizumi, N.; Ichiba, T. Free radical scavenging action of the medicinal herb Limonium wrightii from the Okinawa islands. Phytomed. Int. J. Phytother. Phytopharmacol. 2002, 9, 239–244. [Google Scholar] [CrossRef] [PubMed]
- Falleh, H.; Jalleli, I.; Ksouri, R.; Boulaaba, M.; Guyot, S.; Magne, C.; Abdelly, C. Effect of salt treatment on phenolic compounds and antioxidant activity of two Mesembryanthemum edule provenances. Plant Physiol. Biochem. PPB 2012, 52, 1–8. [Google Scholar] [CrossRef] [PubMed]
- Ksouri, R.; Falleh, H.; Megdiche, W.; Trabelsi, N.; Mhamdi, B.; Chaieb, K.; Bakrouf, A.; Magne, C.; Abdelly, C. Antioxidant and antimicrobial activities of the edible medicinal halophyte Tamarix gallica L. and related polyphenolic constituents. Food Chem. Toxicol. Int. J. Publ. Br. Ind. Biol. Res. Assoc. 2009, 47, 2083–2091. [Google Scholar] [CrossRef] [PubMed]
- Trabelsi, N.; Falleh, H.; Jallali, I.; Daly, A.B.; Hajlaoui, H.; Smaoui, A.; Abdelly, C.; Ksouri, R. Variation of phenolic composition and biological activities in Limoniastrum monopetalum L. organs. Acta Physiol. Plant. 2011, 34, 87–96. [Google Scholar] [CrossRef]
- Meot-Duros, L.; Magne, C. Antioxidant activity and phenol content of Crithmum maritimum L. leaves. Plant Physiol. Biochem. PPB 2009, 47, 37–41. [Google Scholar] [CrossRef] [PubMed]
- Han, Y.-T.; Han, Z.-W.; Yu, G.-Y.; Wang, Y.-J.; Cui, R.-Y.; Wang, C.-B. Inhibitory effect of polypeptide from Chlamys farreri on ultraviolet A-induced oxidative damage on human skin fibroblasts in vitro. Pharmacol. Res. 2004, 49, 265–274. [Google Scholar] [CrossRef] [PubMed]
- Wang, C.-B.; Ding, B.-X.; Guo, S.-B.; Wang, Y.-Z.; Han, Y.-T.; Wang, Y.-J. Protective Effect of Polypeptide From Chlamys Farreri on Mitochondria in Human Dermal Fibroblasts Irradiated by Ultraviolet B. Acta Pharmacol. Sin. 2003, 692–696. [Google Scholar]
- Zhuang, Y.; Hou, H.; Zhao, X.; Zhang, Z.; Li, B. Effects of collagen and collagen hydrolysate from jellyfish (Rhopilema esculentum) on mice skin photoaging induced by UV irradiation. J. Food Sci. 2009, 74, H183–H188. [Google Scholar] [CrossRef] [PubMed]
- Chen, T.; Hou, H. Protective effect of gelatin polypeptides from Pacific cod (Gadus macrocephalus) against UV irradiation-induced damages by inhibiting inflammation and improving transforming growth factor-beta/Smad signaling pathway. J. Photochem. Photobiol. B Biol. 2016, 162, 633–640. [Google Scholar] [CrossRef] [PubMed]
- Shibuya, S.; Ozawa, Y.; Toda, T.; Watanabe, K.; Tometsuka, C.; Ogura, T.; Koyama, Y.; Shimizu, T. Collagen peptide and vitamin C additively attenuate age-related skin atrophy in Sod1-deficient mice. Biosci. Biotechnol. Biochem. 2014, 78, 1212–1220. [Google Scholar] [CrossRef] [PubMed]
- Chen, H.-W.; Yang, T.-S.; Chen, M.-J.; Chang, Y.-C.; Wang, E.I.C.; Ho, C.-L.; Lai, Y.-J.; Yu, C.-C.; Chou, J.-C.; Chao, L.K.-P.; et al. Purification and immunomodulating activity of C-phycocyanin from Spirulina platensis cultured using power plant flue gas. Proc. Biochem. 2014, 49, 1337–1344. [Google Scholar] [CrossRef]
- Pangestuti, R.; Kim, S.-K. Biological activities and health benefit effects of natural pigments derived from marine algae. J. Funct. Foods 2011, 3, 255–266. [Google Scholar] [CrossRef]
- Pandey, G.; Fatma, T.; Cowsik, S.M.; Komath, S.S. Specific interaction of jacalin with phycocyanin, a fluorescent phycobiliprotein. J. Photochem. Photobiol. B Biol. 2009, 97, 87–93. [Google Scholar] [CrossRef] [PubMed]
- Gastineau, R.; Turcotte, F.; Pouvreau, J.B.; Morancais, M.; Fleurence, J.; Windarto, E.; Prasetiya, F.S.; Arsad, S.; Jaouen, P.; Babin, M.; et al. Marennine, promising blue pigments from a widespread Haslea diatom species complex. Mar. Drugs 2014, 12, 3161–3189. [Google Scholar] [CrossRef] [PubMed]
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Guillerme, J.-B.; Couteau, C.; Coiffard, L. Applications for Marine Resources in Cosmetics. Cosmetics 2017, 4, 35. https://doi.org/10.3390/cosmetics4030035
Guillerme J-B, Couteau C, Coiffard L. Applications for Marine Resources in Cosmetics. Cosmetics. 2017; 4(3):35. https://doi.org/10.3390/cosmetics4030035
Chicago/Turabian StyleGuillerme, Jean-Baptiste, Céline Couteau, and Laurence Coiffard. 2017. "Applications for Marine Resources in Cosmetics" Cosmetics 4, no. 3: 35. https://doi.org/10.3390/cosmetics4030035
APA StyleGuillerme, J. -B., Couteau, C., & Coiffard, L. (2017). Applications for Marine Resources in Cosmetics. Cosmetics, 4(3), 35. https://doi.org/10.3390/cosmetics4030035