Inflammatory skin diseases represent a significant health concern, affecting approximately 20–25% of the global population. These conditions not only reduce an individual's quality of life but also impose a huge burden on both humanity and society. However, addressing these challenges is hindered by their chronic nature, insufficient therapeutic effectiveness, and the propensity for recurrence and adverse side effects. Hyaluronic acid (HA) has emerged as a potential solution to these barriers, owing to its excellent attributes such as biocompatibility, non-toxicity, and targeted drug delivery. However, its practical application has been limited because endogenous hyaluronidase (HYAL) rapidly degrades HA in inflamed skin thus reducing its ability to penetrate deep into the skin. Interestingly, recent research has expanded the role of self-assembled HA-nanoparticles (HA-NPs) beyond drug carriers; they are resistant to HYAL, thereby enabling deep skin penetration, and possess inherent anti-inflammatory properties. Moreover, these abilities can be fine-tuned depending on the conditions during particle synthesis. Additionally, their role as a drug delivery system holds potential for use as a multi-target drug or hybrid drug. In conclusion, this review aims to specifically introduce and highlight the emerging potential of HA-NPs as a topical treatment for inflammatory skin conditions.
This study was supported by the Basic Science Research Program (NRF- 2023R1A2C2006174 and RS-2023-00248399 ) and Korea Initiative for fostering University of Research and Innovation Program ( NRF-2021M3H1A104892211 ) through the National Research Foundation of Korea (NRF), funded by the Ministry of Science and ICT and the Ministry of Education . This work was also supported by the Korea Drug Development Fund funded by Ministry of Science and ICT , Ministry of Trade, Industry and Energy , and Ministry of Health and Welfare ( RS-2021-DD120838 ), and was supported by the GRRC program of Gyeonggi province ( GRRCAjou2023-B01 ). The authors thank Dr. E. K. Lee (The Catholic University of Korea) and S. Han (The Catholic University of Korea) for their assistance with RNA-Seq analysis.This study was supported by the Basic Science Research Program (NRF-2023R1A2C2006174 and RS-2023-00248399) and Korea Initiative for fostering University of Research and Innovation Program (NRF-2021M3H1A104892211) through the National Research Foundation of Korea (NRF), funded by the Ministry of Science and ICT and the Ministry of Education. This work was also supported by the Korea Drug Development Fund funded by Ministry of Science and ICT, Ministry of Trade, Industry and Energy, and Ministry of Health and Welfare (RS-2021-DD120838), and was supported by the GRRC program of Gyeonggi province (GRRCAjou2023-B01). The authors thank Dr. E. K. Lee (The Catholic University of Korea) and S. Han (The Catholic University of Korea) for their assistance with RNA-Seq analysis.