JOURNAL OF COSMETIC SCIENCE 64 (26 ) Y. Satomi, Antitumor and cancer-preventative function of fucoxanthin: a marine carotenoid, Anticancer Res., 37, 1557–1562 (2017). (27 ) I. K. Mok, J. R. Yoon, C. H. Pan, and S. M. Kim, Development, quantifi cation, method validation, and stability study of a novel fucoxanthin-fortifi ed milk, J. Agric. Food Chem., 64, 6196–6202 (2016). (28 ) G. J. Fisher, S. C. Datta, H. S. Talwar, Z. Q. Wang, J. Varani, S. Kang, and J. J. Voorhees, Molecular basis of sun-induced premature skin ageing and retinoid antagonism, Nature, 379, 335–339 (1996). (29 ) R. Pallela, Y. Na-Young, and S. K. Kim, Anti-photoaging and photoprotective compounds derived from marine organisms, Mar. Drugs, 8, 1189–1202 (2010). (30 ) M. Manela-Azulay and E. Bagatin, Cosmeceuticals vitamins, Clin. Dermatol., 27, 469–474 (2009). (31 ) Y. Liu, J. Zheng, Y. Zhang, Z. Wang, Y. Yang, M. Bai, and Y. Dai, Fucoxanthin activates apoptosis via inhibition of PI3K/Akt/mTOR pathway and suppresses invasion and migration by restriction of p38- MMP-2/9 pathway in human glioblastoma cells, Neurochem. Res., 41, 2728–2751 (2016). (32 ) S. K. Wang, Y. Li, W. L. White, and J. Lu, Extracts from New Zealand Undaria pinnatifi da containing fucoxanthin as potential functional biomaterials against cancer in vitro, J. Funct. Biomater., 5, 29–42 (2014). (33 ) C. Ishikawa, S. Tafuku, T. Kadekaru, S. Sawada, M. Tomita, T. Okudaira, T. Nakazato, T. Toda, J. N. Uchihara, N. Taira, K. Ohshiro, T. Yasumoto, T. Ohta, and N. Mori, Anti-adult T-cell leukemia effects of brown algae fucoxanthin and its deacetylated product, fucoxanthinol, Int. J. Cancer, 123, 2702–2712 (2008). (34 ) K. Yamamoto, C. Ishikawa, H. Katano, T. Yasumoto, and N. Mori, Fucoxanthin and its deacetylated product, fucoxanthinol, induce apoptosis of primary effusion lymphomas, Cancer Lett., 300, 225–234 (2011). (35 ) F. Beppu, Y. Niwano, T. Tsukui, M. Hosokawa, and K. Miyashita, Single and repeated oral dose toxicity study of fucoxanthin (FX), a marine carotenoid, in mice, J. Toxicol. Sci. 34, 501–510 (2009). (36 ) K. Iio, Y. Okada, and M. Ishikura, [Bacterial reverse mutation test and micronucleus test of fucoxanthin oil from microalgae], Shokuhin Eiseigaku Zasshi, 52, 190–193 (2011). (37) B. A. Booth, K. L. Polak, and J. Uitto, Collagen biosynthesis by human skin fi broblasts. I. Optimiza- tion of the culture conditions for synthesis of type I and type III procollagens, Biochim. Biophys. Acta., 607, 145–160 (1980). (38 ) H. Nagase and J. F. Woessner, Jr., Matrix metalloproteinases, J. Biol. Chem., 274, 21491–21494 (1999). (39 ) K. Scharffetter-Kochanek, P. Brenneisen, J. Wenk, G. Herrmann, W. Ma, L. Kuhr, C. Meewes, and M. Wlaschek, Photoaging of the skin from phenotype to mechanisms, Exp. Gerontol., 35, 307–316 (2000). (40 ) E. I. Deryugina and J. P. Quigley, Matrix metalloproteinases and tumor metastasis, Cancer Metastasis Rev., 25, 9–34 (2006). (41 ) S. R. Kumar, M. Hosokawa, and K. Miyashita, Fucoxanthin: a marine carotenoid exerting anti-cancer effects by affecting multiple mechanisms, Mar. Drugs, 11, 5130–5147 (2013). (42 ) T. W. Chung, H. J. Choi, J. Y. Lee, H. S. Jeong, C. H. Kim, M. Joo, J. Y. Choi, C. W. Han, S. Y. Kim, J. S. Choi, and K. T. Ha, Marine algal fucoxanthin inhibits the metastatic potential of cancer cells, Biochem. Biophys. Res. Commun., 439, 580–585 (2013). (43 ) F. A. Simion, E. S. Abrutyn, and Z. D. Draelos, Ability of moisturizers to reduce dry skin and irritation and to prevent their return, J. Cosmet. Sci., 56, 427–444 (2005). (44 ) M. Guzmán-Alonso and T. M. Cortazár, Water content at different skin depths and the infl uence of moisturizing formulations, Househ. Pers. Care Today, 11, 35–40 (2016). (45) Z . X. Jiang and J. DeLaCruz, Appearance benefi ts of skin moisturization, Skin Res. Technol., 17, 51–55 (2011). (46) S . Verdier-Sévrain and F. Bonté, Skin hydration: a review on its molecular mechanisms, J. Cosmet. Der- matol., 6, 75–82 (2007). (47) C. R. Harding and I. R. Scott, Histidine-rich proteins (fi laggrins): structural and functional heterogene- ity during epidermal differentiation, J. Mol. Biol., 170, 651–673 (1983). (48) A. Sandilands, C. Sutherland, A. D. Irvine, and W. H. McLean, Filaggrin in the frontline: role in skin barrier function and disease, J. Cell. Sci., 122, 1285–1294 (2009). (49) M. Matsui, K. Tanaka, N. Higashiguchi, H. Okawa, Y. Yamada, K. Tanaka, S. Taira, T. Aoyama, M. Takanishi, C. Natsume, Y. Takakura, N. Fujita, T. Hashimoto, and T. Fujita, Protective and therapeutic effects of fucoxanthin against sunburn caused by UV irradiation, J. Pharmacol. Sci., 132, 55–64 (2016).
J. Cosmet. Sci., 71, 65–75 (March/April 2020) 65 Synthesis of 5-Aminolevulinic Acid–Based ALACELL Possessing Inhibitory Effect against Cutibacterium acnes: Whitening Effect and Protective Effect of UVB-Irradiated Damage Cells HYUN-YOUNG KIM, SU-JUNG KIM, HWA-JUNG CHOI, and SOON-HO YIM , Department of Pharmaceutical Engineering, Dongshin University, Jeonnam, 58245 South Korea (H.-Y.K., S.-H.Y.), School of Biological Sciences and Biotechnology Graduate School, Chonnam National University , Gwangju, 61186 South Korea (S.-J.K.), Department of Beauty Science, Kwangju Women’s University, Gwangju 62396, South Korea (H.-J.C.) Accepted for publication January 23, 2020 . Synopsis Five-aminolevulinic acid (5-ALA)-photodynamic therapy combined with infrared radiation is an effective and safe therapy for facial acne. Although there are various available agents for treating acne, therapies for resistant or severe strains have been limited. The aim of this study was to investigate the inhibitory effi cacy of ALACELL synthesized by combining 5-ALA with Y-G-G-F-L peptide against Staphylococcus aureus, Bacillus cereus, Escherichia coli, and Yersinia enterocolitica, as well as Cutibacterium acnes. Furthermore, other effects of ALACELL on human skin cells, melanin formation, intracellular tyrosinase activity, and Ultra Violet B (UVB)- irradiated cell death were measured by treatment of ALACELL in vitro. ALACELL particularly showed a growth inhibitory effect on C. acnes and no inhibitory effect on the four bacteria strains. ALACELL reduced melanin formation and intracellular tyrosinase activity by α-melanin cell–stimulating hormone (α-MSH) in B16F10 cells, with no cytotoxicity. ALACELL also improved cell viability in UVB-irradiated HaCaT cells. The results of the experiment show that ALACELL exhibits more effi cacy than 5-ALA against antimicrobial activity, melanin formation, intracellular tyrosinase activity, and UVB-irradiated cell death. Therefore, ALACELL is recommended as a candidate for clinical application in the treatment of acne and skin aging and will be further investigated to study the mode of action and in actual situations. IN T RODUCTION Al l humans have a variety of micro-organisms on the skin that constitute the skin micro- biome and that might play a role in skin immunity and skin barrier (1). Systemic imbalances in this skin have been related to dermatologic disease problems, such as acne and atopic dermatitis (2). Address all correspondence to Soon-Ho Yim at virshyim@gmail.com . Hyun-Young Kim and Su-Jung Kim contributed equally to this work.
Purchased for the exclusive use of nofirst nolast (unknown) From: SCC Media Library & Resource Center (library.scconline.org)




































































