Facile synthetic nano-curcumin encapsulated Bio-fabricated nanoparticles induces ROS-mediated apoptosis and migration blocking of human lung cancer cells

被引:20
|
作者
Dong, Yuehua [1 ]
Yang, Yanjun [1 ]
Wei, Yulei [1 ]
Gao, Yongshan [1 ]
Jiang, Weihua [1 ]
Wang, Guigang [1 ]
Wang, Dawei [1 ]
机构
[1] Hebei North Univ, Dept Cardiothorac Surg, Affiliated Hosp 1, Zhangjiakou, Peoples R China
关键词
Zinc; Curcumin; Lung cancers; Apoptosis; ROS; Hemolysis; MESOPOROUS SILICA NANOPARTICLES; DRUG-RELEASE; DELIVERY; BREAST; THERAPY; NANOCARRIERS; NANOPLATFORM; COMPLEXES; CISPLATIN; AUTOPHAGY;
D O I
10.1016/j.procbio.2020.05.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lung cancer is one of the major life-threatening cancers, with a higher mortality rate and morbidity. Curcumin acts as a potential anticancer agent but it shows less aqueous solubility so its clinical application is limited. In this present study, we developed curcumin-surface decorated Zinc Oxide nanoparticles ZnO@Cur to enhance its aqueous formulation and improve the anti-cancer activity of curcumin. The synthesized ZnO@Cur confirmed by various spectroscopies (UV-vis and fluorescence) and electroscopic techniques (Powder XRD, SEM, TEM, and DLS). ZnO@Cur dramatically suppressed the proliferation of A549 and HEL-299 cells and showed low toxicity in MTT assays. Compared with free ZnO and curcumin, ZnO@Cur significantly inhibited the migration ability of A549 cells. Moreover, the induction of apoptosis in A549 cells by ZnO@Cur was resulted by AO-EB staining. ZnO@Cur activated to promote intracellular ROS overproduction and induced apoptosis. ZnO@Cur shows excellent biocompatibility compared to free ZnO and Curcumin, the present study explained that ZnO@Cur as a safe and hopeful strategy for chemotherapeutics of lung cancer therapy and deserve for further clinical evaluations.
引用
收藏
页码:91 / 98
页数:8
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