Chitosan-capped silver nanoparticles with potent and selective intrinsic activity against the breast cancer cells

被引:16
|
作者
Abdellatif, Ahmed A. H. [1 ,2 ]
Abdelfattah, Ahmed [3 ]
Younis, Mahmoud A. [3 ]
Aldalaan, Saed M. [4 ]
Tawfeek, Hesham M. [3 ]
机构
[1] Qassim Univ, Coll Pharm, Dept Pharmaceut, Qasim 51452, Saudi Arabia
[2] Al Azhar Univ, Fac Pharm, Dept Pharmaceut & Pharmaceut Technol, Assiut 71524, Egypt
[3] Assiut Univ, Fac Pharm, Dept Ind Pharm, Assiut 71526, Egypt
[4] Mutah Univ, Fac Med, Dept Pharmacol, Al Karak 61070, Jordan
关键词
breast cancer; silver nanoparticles; chitosan; IL-6; TNF-alpha; INTERNATIONAL EXPERT CONSENSUS; PRIMARY THERAPY; IN-VITRO; AGGREGATION; GOLD; ANTIBACTERIAL; CYTOTOXICITY; CAPACITY; DELIVERY; ALPHA;
D O I
10.1515/ntrev-2022-0546
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report on the development of chitosan-capped silver nanoparticles (AgNPs-CHI) with an intrinsic activity against breast cancer cells. Following chemical synthesis via a simple, one-pot reaction, the chitosan coating of AgNPs was verified using Fourier-transform infrared and ultraviolet-visible spectroscopies. The physicochemical properties and morphology were characterized using dynamic light scattering, scanning electron microscopy, and transmission electron microscopy. The shelf stability of the optimized platform was tracked for 3 months upon storage at either room temperature or 4 degrees C. Then, the anticancer activities of AgNPs-CHI on human breast cancer cells, MCF-7, versus normal human cells, human skin fibroblasts (HSF), were evaluated via 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide cytotoxicity assay and tumor-associated biomarkers determination by enzyme-linked immunosorbent assay, in comparison with plain silver nitrate (AgNO3) solution. AgNPs were successfully coated with chitosan and demonstrated acceptable physicochemical properties, with a spherical morphology and high stability upon long-term storage. Although AgNPs-CHI and AgNO3 demonstrated comparable cytotoxicity to MCF-7 cells, AgNPs-CHI resulted in 10-fold lower toxicity to HSF cells, suggesting a higher selectivity. In addition, AgNPs-CHI lowered IL-6 and tumor necrosis factor-alpha levels in MCF-7 cells by 90 and 30%, respectively, compared to 60 and 10% in the case of plain AgNO3. The interesting therapeutic modality presented in this study is promising for potential clinical applications.
引用
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页数:12
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