Investigation into the anticancer activity of biosynthesized zinc oxide nanoparticles incorporating ۶-gingerols

سال انتشار: 1404
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 148

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شناسه ملی سند علمی:

JR_CMBR-5-3_003

تاریخ نمایه سازی: 13 اردیبهشت 1404

چکیده مقاله:

Ginger is a popular spice, and ۶-gingerol (۶-Gin) is a bioactive phenolic compound. The compound ۶-Gin exhibits certain drawbacks, including poor solubility in water and sensitivity to temperature, pH, and oxygen. To overcome these challenges, a novel green method has been developed to produce zinc oxide nanoparticles (ZnO-NPs) modified with chitosan and folate, which can effectively deliver ۶-Gin (۶-Gin-CZF-NPs) and enhance its anticancer properties. The nanoparticles were initially synthesized and subsequently surface-modified. Their physicochemical properties were assessed using various methods. The size of the ۶-Gin-CZF-NPs was measured at ۱۱۰.۶۶ nm, exhibiting a smooth surface and a spherical shape. The surface potential of the nanoparticles was reported to be +۲۹ mV, and the drug encapsulation efficiency was ۸۶.۹%. The antioxidant properties and anticancer effects of the ۶-Gin-CZF-NPs were evaluated. The cytotoxic effects of the ۶-Gin-CZF-NPs on breast, stomach, and colon cancer cells were compared to those on HFF cells, yielding IC۵۰ values of ۹۴.۴, ۱۸۰.۵, and ۳۶۹.۲ μg/mL, respectively. Results from DAPI staining and flow cytometry indicated that in the treated groups, apoptosis increased with higher concentrations, leading to an accumulation of treated cells in the SubG۱ phase. The increase in Caspase ۳, ۸, and ۹ further confirmed the pro-apoptotic activity of the ۶-Gin-CZF-NPs. This inhibition of cancer cells occurs through the induction of apoptosis via both intrinsic and extrinsic pathways. The IC۵۰ values for ABTS and DPPH assays were ۱۹۷.۷ and ۴۷۵.۳ µg/mL, respectively. The results regarding antioxidant activity, cytotoxicity, and apoptosis of these newly prepared nanoparticles confirm their anticancer efficacy, particularly against breast cancer cells.

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نویسندگان

Noor Hayder Mohammed Al-Hamadani

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran

Vahid Pouresmaeil

Department of Biochemistry, Faculty of Medicine, Mashhad Medical Sciences, Islamic Azad University, Mashhad, Iran

Mahshid Sharbatiyan

Department of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran

Masoud Homayouni Tabrizi

Department of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran

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