纳米载体
卵清蛋白
化学
体内
溃疡性结肠炎
生物利用度
生物相容性
纳米颗粒
水溶液
没食子酸表没食子酸酯
肿瘤坏死因子α
药理学
药物输送
生物物理学
纳米技术
多酚
材料科学
生物化学
免疫系统
免疫学
有机化学
医学
抗氧化剂
生物技术
病理
生物
疾病
作者
Shuangquan Gou,Qiubing Chen,Yan Liu,Liang Zeng,Heliang Song,Zhigang Xu,Yuejun Kang,Chang Ming Li,Bo Xiao
标识
DOI:10.1021/acssuschemeng.8b01613
摘要
Nanoparticles (NPs) have the capacity to improve the bioactivity and bioavailability of anti-inflammatory drugs. Here, a green drug nanocarrier based on ovalbumin (OVA) was facilely produced via a self-assembling process by adding epigallo-catechin 3-gallate (EGCG) aqueous solution to OVA aqueous solution at 80 °C. The obtained EGCG-NPs had an average hydrodynamic diameter (around 202.9 nm), negative surface charge (approximately −13.2 mV), high EGCG encapsulation efficiency (98.1%), and reduction-responsive EGCG release capacity. Additionally, they possessed excellent biocompatibility and achieved a much higher cellular uptake rate of EGCG than pristine EGCG. Furthermore, EGCG-NPs had remarkably stronger capacity to suppress the secretion of pro-inflammatory mediators (e.g., tumor necrosis factor α, interleukin-6, interleukin-12) and promote the production of anti-inflammatory factor (interleukin-10), in comparison with pristine EGCG. Finally, in vivo experiments demonstrated the excellent therapeutic efficacy of EGCG-NPs in alleviating ulcerative colitis (UC). The present study collectively suggests that these facilely fabricated OVA-based NPs could be exploited as an efficient EGCG carrier for UC therapy.
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