Kim Kyu-Lim, Jeon Ju-Hee, Kim Yeonjoon, Lim Kyung-Min
College of Pharmacy, Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Republic of Korea.
Graduate Program in Innovative Biomaterials Convergence, Ewha Womans University, Seoul 03760, Republic of Korea.
Antioxidants (Basel). 2025 Jun 29;14(7):806. doi: 10.3390/antiox14070806.
Caffeic acid (CA) is a naturally occurring polyphenol antioxidant found in coffee, tea, fruits, and vegetables, known for its strong antioxidant, anti-inflammatory, and anti-aging properties. However, its cosmetic application is limited because of poor dermal absorption due to its high polarity. This study aimed to evaluate the antioxidant and skin-brightening effects of a novel lipophilic CA derivative, CAD (caffeic acid-3,4-dihydroxyphenylpropanolester). CAD was synthesized by conjugating CA with 3,4-DHPEA, a lipophilic antioxidant derived from olive oil. In both DPPH and ABTS assays, CAD exhibited more potent antioxidant activity than CA. In B16F10 melanoma cells, CAD significantly inhibited melanin production without cytotoxicity at concentrations lower than those required for CA. Cellular assays using DCF-DA staining demonstrated that CAD effectively reduced intracellular ROS levels. Mechanistic studies revealed that CAD inhibited tyrosinase activity and downregulated the expression of TYR, TRP-1, and TRP-2. Additionally, CAD suppressed MITF phosphorylation, along with reduced phosphorylation of ERK and JNK, elucidating its anti-melanogenic mechanism. Importantly, CAD showed dose-dependent skin-brightening effects in the 3D human skin model Melanoderm™, as evidenced by increased lightness and histological evaluation. In conclusion, CAD demonstrates strong potential as a safe and effective antioxidant and skin-brightening agent for cosmetic applications.
咖啡酸(CA)是一种天然存在的多酚抗氧化剂,存在于咖啡、茶、水果和蔬菜中,以其强大的抗氧化、抗炎和抗衰老特性而闻名。然而,由于其高极性导致皮肤吸收性差,其在化妆品中的应用受到限制。本研究旨在评估一种新型亲脂性咖啡酸衍生物CAD(咖啡酸-3,4-二羟基苯丙醇酯)的抗氧化和亮肤效果。CAD是通过将CA与3,4-DHPEA(一种源自橄榄油的亲脂性抗氧化剂)共轭合成的。在DPPH和ABTS测定中,CAD均表现出比CA更强的抗氧化活性。在B16F10黑色素瘤细胞中,CAD在低于CA所需浓度时能显著抑制黑色素生成且无细胞毒性。使用DCF-DA染色的细胞实验表明,CAD能有效降低细胞内ROS水平。机制研究表明,CAD抑制酪氨酸酶活性并下调TYR、TRP-1和TRP-2的表达。此外,CAD抑制MITF磷酸化,同时降低ERK和JNK的磷酸化,阐明了其抗黑色素生成机制。重要的是,在3D人体皮肤模型Melanoderm™中,CAD呈现出剂量依赖性的亮肤效果,这通过明度增加和组织学评估得到证实。总之,CAD作为一种安全有效的抗氧化剂和亮肤剂在化妆品应用中显示出强大的潜力。