作者
Wang Hee Lee,Jun Gi Rho,Yeyoung Yang,Seulbi Lee,Sohui Kweon,Hyung‐Mo Kim,Juhwan Yoon,Hongseo Choi,Eunyoung Lee,Su Ha Kim,Sohee You,Yu-Jin Song,Young Soo Oh,Il Hwan Kim,Hwa Seung Han,Ji Hye Han,Myeongwoo Jung,Young Hwan Park,Yang Seon Choi,Sukyoung Han,Jun-Ho Lee,Sangdun Choi,Jung-Woong Kim,Jae Hyung Park,Eun Kyung Lee,Woo Keun Song,Eunha Kim,Wook Kim
摘要
Although conventional topical approaches for treating psoriasis have been offered as an alternative, there are still unmet medical needs such as low skin-penetrating efficacy and off-target adverse effects. A hyaluronic acid nanoparticle (HA-NP) formed by self-assembly of HA-hydrophobic moiety conjugates has been broadly studied as a nanocarrier for long-term and target-specific delivery of drugs, owing to their excellent physicochemical and biological characteristics. Here, we identify HA-NPs as topical therapeutics for treating psoriasis using in vivo skin penetration studies and psoriasis animal models. Transcutaneously administered HA-NPs were found to be accumulated and associated with pro-inflammatory macrophages in the inflamed dermis of a psoriasis mouse model. Importantly, HA-NP exerted potent therapeutic efficacy against psoriasis-like skin dermatitis in a size-dependent manner by suppressing innate immune responses and restoring skin barrier function without overt toxicity signs. The therapeutic efficacy of HA-NPs on psoriasis-like skin dermatitis was due to the outermost hydrophilic HA shell layer of HA-NPs, independent of the molecular weight of HA and hydrophobic moiety, and comparable with that of other conventional psoriasis therapeutics widely used in the clinical settings. Overall, HA-NPs have the potential as a topical nanomedicine for treating psoriasis effectively and safely.