Hyaluronic acid-based supramolecular medicine with polyamines sequestration capability for cooperative anti-psoriasis

被引:13
作者
Ding, Yuan-Fu [1 ,2 ]
Wei, Jianwen [1 ]
Quan, Xingping [1 ]
Gu, Wenting [1 ]
Xi, Long [1 ]
Zheng, Ying [1 ,3 ]
Zhao, Yonghua [1 ,3 ]
Luo, Jingwei [4 ]
Li, Shengke [1 ]
Mok, Greta S. P. [2 ]
Wang, Ruibing [1 ,3 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Taipa, Macao, Peoples R China
[2] Univ Macau, Dept Elect & Comp Engn, Biomed Imaging Lab BIG, Taipa, Macao, Peoples R China
[3] Univ Macau, Fac Hlth Sci, Dept Pharmaceut Sci, Taipa, Macao, Peoples R China
[4] UltraSpec Lab, Victoria, BC V8P 2N1, Canada
基金
中国国家自然科学基金;
关键词
CD-44; targeting; Host-guest interactions; Controlled release; Polyamine sequestration; Cooperative anti-psoriasis; CURCUMIN; CELLS; DRUG; OXALIPLATIN; MECHANISMS; RELEASE;
D O I
10.1016/j.carbpol.2022.119968
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Psoriasis seriously harms physical and mental health of patients. Hyaluronic acid (HA)-based topical formulation can increase drug concentration in psoriatic skin via CD44-assisted targeting. Herein, we developed a supra -molecular medicine composed of curcumin-loaded HA-cucurbit[7]uril (HA-CB[7]@Cur), which could efficiently sequester polyamines (PAs) via host-guest interactions of CB[7] and PAs to suppress RNA-PAs immunocomplex formation. Meanwhile, anti-psoriasis drug Cur could be released from HA-CB[7]@Cur by PAs. With phenotypical disease evaluation, psoriasis area measurements and severity index scoring, and histological characterizations, we demonstrate topical administration of Carbopol gel formulation of HA-CB[7]@Cur on psoriasis-like skin in mice exhibited an enhanced anti-psoriasis activity, in comparison with gel of free Cur or HA-CB[7]. Cytokine expression analysis in psoriatic skin also supported the observed therapeutic outcomes. We provide a novel and effective supramolecular strategy to realize cooperative anti-psoriasis via controlled release of curcumin and PAs sequestration, which can be potentially expanded to treat other PA-involved skin inflammatory diseases.
引用
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页数:9
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