姜黄素
体内
药理学
生物利用度
药品
痛风
化学
关节炎
炎症
促炎细胞因子
秋水仙碱
医学
内科学
生物化学
生物技术
生物
作者
Mei Zhang,Xiaolin Zhang,Taoran Tian,Qi Zhang,Yuting Wen,Junyao Zhu,Dexuan Xiao,Weitong Cui,Yunfeng Lin
标识
DOI:10.1016/j.bioactmat.2021.06.003
摘要
Gouty arthritis is a very familiar inflammatory arthritis. Controlling inflammation is the key to preventing gouty arthritis. However, colchicine, the most highly represented drug used in clinical practice, has strict contraindications owing to some severe side effects. Curcumin (Cur), a natural anti-inflammatory drug, has demonstrated good safety and efficacy. However, the rapid degradation, poor aqueous solubility, and low bioavailability of Cur limit its therapeutic effect. To strengthen the effectiveness and bioavailability of Cur. Cur loaded tetrahedral framework nucleic acids (Cur-TFNAs) were synthesized to deliver Cur. Compared with free Cur, Cur-TFNAs exhibit a preferable drug stability, good biocompatibility (CCK-8 assay), ease of uptake (immunofluorescence), and higher tissue utilization (in vivo biodistribution). Most importantly, Cur-TFNAs present better anti-inflammatory effect than free Cur both in vivo and in vitro experiments through the determination of inflammation-related cytokines expression. Therefore, we believe that Cur-TFNAs have great prospects for the prevention of gout and similar inflammatory diseases.
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