炎症体
药品
脂质体
乙二醇
生物利用度
药理学
材料科学
受体
化学
医学
生物化学
纳米技术
有机化学
作者
Roberto Negro,Rita Mastrogiacomo,Livianna Carrieri,Federica Rizzi,Valentina Arrè,Gianluca Minervini,Elisabetta Fanizza,Giusy Bianco,Annamaria Panniello,Marinella Striccoli,Roberto Comparelli,Ricardo L. Armentano,Maria Lucia Curri,Gianluigi Giannelli,Nicoletta Depalo,Maria Principia Scavo
标识
DOI:10.1021/acsami.3c04206
摘要
Inflammasome activation plays a crucial role in the progression to more severe stages of non-alcoholic fatty liver disease (NAFLD), representing a promising therapeutic target. MCC950 is a small molecule acting as a potent and specific inhibitor of the canonical and non-canonical activation of the NLRP3 inflammasome, but its short plasmatic half-life limits its use. Herein, we report, for the first time, the encapsulation of MCC950 in poly(ethylene glycol) (PEG) liposomes (LPs) that are specifically functionalized with an antibody against Frizzled 1 (FZD1), a g-coupled protein involved in the WNT pathway and overexpressed on inflammasome-activated macrophages. MCC950, encapsulated into PEG-LP formulations conjugated with an anti-FZD1 antibody, inhibits the NLRP3 inflammasome activation at concentrations 10 times lower than that of the free drug in THP-1 cells. Luminescent carbon dots (CDs) were also co-encapsulated with MCC950 in LPs to obtain optically traceable nanoformulations that have proved the enhanced ability of the targeted LPs to be internalized into THP-1 cells with respect to their nontargeted counterparts. Our results suggest that MCC950 encapsulation into targeted LPs represents a valuable strategy to achieve reformulation of the NLRP3 inhibitor, able to significantly curtail the threshold of MCC950 doses for inhibiting inflammasome activation, thus offering a new therapeutic approach.
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