Characterization and Investigation of the Toxicity, Genotoxicity, Antioxidant, and Radical Scavenging Activity of Highly Fluorescent Nitrogen-Doped Graphene Quantum Dots (NGQDs)

سال انتشار: 1404
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 223

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شناسه ملی سند علمی:

JR_IJCCE-44-4_002

تاریخ نمایه سازی: 16 خرداد 1404

چکیده مقاله:

Nitrogen-Doped Graphene Quantum Dots (NGQDs) have recently been used effectively in drug delivery. Our study aimed to characterize NGQDs and investigate their toxicity and genotoxicity using the Brine Shrimp lethality test (BSLT), Allium cepa L assay, and MTT assay on U۲۵۱ GBM cells. NGQDs were synthesized using citric acid and Tris(hydroxymethyl) aminomethane through the pyrolysis method. Antioxidant and scavenging activities of NGQDs were also measured. LC۵۰, EC۵۰, and IC۵۰ of NGQDs were determined; the Allium cepa L assay was also used to explore the potential mutagenic and carcinogenic effects of NGQDs. NGQDs had an average size of ۸.۱±۱ nm with a zeta(ζ)-potential of −۲۴.۴ mV. ATR FT-IR findings demonstrate that NGQDs have functional groups, and TEM analysis revealed heterogeneous morphologies. AFM measurements indicate that the size of the distribution of NGQDs is relatively uniform except for some agglomeration of NGQDs. UV-vis and FL spectra were ۳۳۵ and ۴۱۰ nm, respectively. ABTS+ and DPPH radical scavenging activities were ۴.۱۳±۰.۴ and ۶۱.۳۲±۰.۲۲%, respectively. Total phenol content and antioxidant power were ۲۳±۱.۱۵ µg GAE/g and ۵۷۷.۹۸±۰.۲۸ µmol Fe۲+/g, respectively. LC۵۰, EC۵۰, and IC۵۰ values were ۳۳۸۸.۴±۲۲۴.۳, ۵۸۲۵.۴±۷۰۳.۳, and ۳۰۵۷±۱۵۶.۹ µg/mL, respectively. In conclusion, NGQDs exhibited high photoluminescence and biocompatibility with no significant cytotoxic or genotoxic effects, making them highly safe for drug delivery. Moreover, it was concluded that the BSLT and Allium cepa L assay could be good alternatives to the MTT assay though further research is needed to confirm this.

کلیدواژه ها:

Nitrogen-doped Graphene Quantum Dots (N-GQD) ، Lethal Concentration ۵۰(LC۵۰) ، Half maximal effective concentration (EC۵۰) ، Half-maximal inhibitory concentration (IC۵۰)

نویسندگان

Mehdi Ghavamizadeh

Cellular and Molecular Research Center, Gerash University of Medical Sciences, Gerash, I.R. IRAN

Azam Habibi

Department of Biochemistry, School of Medicine, Autophagy Research Center, Shiraz University of Medical Sciences, Shiraz, I.R. IRAN

Sanaz Dastghaib

Endocrinology and Metabolism Research Center, Shiraz University of Medical Sciences, P.O. Box ۷۱۳۴۵-۱۷۴۴, Shiraz, I.R. IRAN

Mazaher Ahmadi

Faculty of Chemistry and Petroleum Sciences, Bu-Ali Sina University, Hamedan, I.R. IRAN

Pooneh Mokarram

Department of Biochemistry, School of Medicine, Autophagy Research Center, Shiraz University of Medical Sciences, Shiraz, I.R. IRAN

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