Fabrication and evaluation of anticancer potential of diosgenin incorporated chitosan-silver nanoparticles; in vitro, in silico and in vivo studies

体内 磺酰罗丹明B细胞培养试剂染料 薯蓣皂甙元 化学 Zeta电位 空泡化 肝癌 壳聚糖 体外 药理学 细胞毒性 癌症 纳米颗粒 生物 纳米技术 医学 病理 生物化学 材料科学 生物技术 内科学 有机化学
作者
Sumera Zaib,Hamid Saeed Shah,Imtiaz Khan,Zobia Jawad,Muhammad Sarfraz,Huma Riaz,Hafiz Muhammad Mazhar Asjad,Memoona Ishtiaq,Hanan A. Ogaly,Mohamed I. A. Othman,Dalia Abd El Moneim Ahmed
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:254: 127975-127975 被引量:1
标识
DOI:10.1016/j.ijbiomac.2023.127975
摘要

The discovery of effective therapeutic approaches with minimum side effects and their tendency to completely eradicate the disease is the main challenge in the history of cancer treatment. Fenugreek (FGK) seeds are a rich source of phytochemicals, especially Diosgenin (DGN), which shows outstanding anticancer activities. In the present study, chitosan-silver nanoparticles (ChAgNPs) containing Diosgenin (DGN-ChAgNPs) were synthesized and evaluated for their anticancer activity against breast cancer cell line (MCF-7). For the physical characterization, the hydrodynamic diameter and zeta potential of DGN-ChAgNPs were determined to be 160.4 ± 12 nm and +37.19 ± 5.02 mV, respectively. Transmission electron microscopy (TEM) showed that nanoparticles shape was mostly round with smooth edges. Moreover, DGN was efficiently entrapped in nanoformulation with good entrapment efficacy (EE) of ~88 ± 4 %. The in vitro anti-proliferative activity of DGN-ChAgNPs was performed by sulforhodamine B (SRB) assay with promising inhibitory concentration of 6.902 ± 2.79 μg/mL. DAPI staining, comet assay and flow cytometry were performed to validate the anticancer potential of DGN-ChAgNPs both qualitatively and quantitatively. The percentage of survival rate and tumor reduction weight was evaluated in vivo in different groups of mice. Cisplatin was used as a standard anticancer drug. The DGN-ChAgNPs (12.5 mg/kg) treated group revealed higher percentage of survival rate and tumor reduction weight as compared to pure DGN treated group. These findings suggest that DGN-ChAgNPs could be developed as potential treatment therapy for breast cancer.
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