4.8 Article

Hyaluronic Acid Nanoparticles as a Topical Agent for Treating Psoriasis

期刊

ACS NANO
卷 -, 期 -, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c07843

关键词

hyaluronic acid; self-assembled nanoparticle; skin barrier function; skin inflammation; topical therapeutics; psoriasis

资金

  1. Basic Science Research & Development Program
  2. Creative Materials Discovery Program through the National Research Foundation of Korea (NRF)
  3. Commercialization Promotion Agency for R&D Outcomes (COMPA) - Ministry of Education [2019R1A6A1A11051471, 2021M3H1A1048922, 2021M3A9G1015618]
  4. Ministry of Science and ICT [2021M3A9G1015618, 2016R1A5A1007318, 2019M3E5D5066526, 2019R1A2B-5B03100464, 2019M3D1A1078941, 2020R1C1C1010044]
  5. Korea Drug Development Fund - Ministry of Science and ICT
  6. Ministry of Trade, Industry, and Energy
  7. Ministry of Health and Welfare [HN21C0958]
  8. National Research Foundation of Korea [2019M3E5D5066526, 2020R1C1C1010044, 2021M3A9G1015618] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Hyaluronic acid nanoparticles (HA-NPs) have been identified as a potential topical nanomedicine for effectively and safely treating psoriasis by suppressing immune responses and restoring skin barrier function without causing overt toxicity.
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 longterm 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.

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