Yang Guangpu, Li Yixuan, Tian Jingwen, Ding Wenxiu, Li Xiuxiu, Ma Xuanxuan, Wei Tao, Xu Jing
Shandong Provincial Key Laboratory of Natural Molecule Discovery and Delivery, School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250353, P. R. China.
Macromol Biosci. 2026 Jan;26(1):e00485. doi: 10.1002/mabi.202500485.
Transdermal peptides, Engineered from bioactive peptides through rational sequence modification and structural optimization, transdermal peptides have emerged as a transformative strategy for enhancing the transdermal delivery of macromolecular drugs, proteins, and nucleic acids. This review outlines the structural classifications of bioactive peptides, including short, linear, cyclic, cationic, anionic, and neutral peptides, as well as their diverse biological sources. It focuses on the design principles and penetration mechanisms of transdermal peptides. These peptides interact dynamically with skin constituents, such as lipids and keratins, by fine-tuning the hydrophilic-hydrophobic balance, molecular weight, and conformational stability. This transiently disrupts the stratum corneum barrier and facilitates drug permeation via endocytosis and receptor-mediated pathways. They find applications in various pharmaceutical domains, including localized anticancer and antimicrobial therapies, as well as in cosmetics for whitening, anti-aging, and moisturizing. They are also being explored in innovative areas such as hair regeneration and wound healing. When combined with advanced delivery platforms, such as nanocarriers, microneedles, and microfluidic systems, transdermal peptides can significantly improve targeting efficacy and enable controlled release. Despite challenges related to peptide immunogenicity and scalable synthesis, the future integration of smart, stimuli-responsive technologies and artificial intelligence promises to Bioactive peptides, Skin permeation mechanisms, Skin transmission, Transdermal peptidesadvance personalized transdermal therapeutics.
透皮肽是通过合理的序列修饰和结构优化从生物活性肽工程化而来的,已成为增强大分子药物、蛋白质和核酸透皮递送的变革性策略。本综述概述了生物活性肽的结构分类,包括短肽、线性肽、环肽、阳离子肽、阴离子肽和中性肽,以及它们多样的生物来源。它重点关注透皮肽的设计原理和渗透机制。这些肽通过微调亲水-疏水平衡、分子量和构象稳定性,与皮肤成分如脂质和角蛋白动态相互作用。这会暂时破坏角质层屏障,并通过内吞作用和受体介导的途径促进药物渗透。它们在各种制药领域有应用,包括局部抗癌和抗菌治疗,以及在美白、抗衰老和保湿的化妆品中。它们也在毛发再生和伤口愈合等创新领域进行探索。当与纳米载体、微针和微流控系统等先进递送平台结合时,透皮肽可以显著提高靶向效果并实现控释。尽管存在与肽免疫原性和可扩展合成相关的挑战,但智能、刺激响应技术和人工智能的未来整合有望推动个性化透皮治疗。生物活性肽、皮肤渗透机制、皮肤传递、透皮肽