International journal of nanomedicine · 2026
Magnesium Oxide Nanoparticles Loaded with 6-Gingerol: A Bioinspired Approach to Anticancer, Anti-Inflammatory, and Antioxidant Therapy.
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Kamaraj Chinnaperumal, Yanto Dede Heri Yuli, Kumarasamy Vinoth, Al-Ghanim Khalid A, Subramaniyan Vetriselvan, Wong Ling Shing, Vetrivel Cittrarsu
Аннотация
PURPOSE: The aim of this work is to synthesize magnesium oxide nanoparticles (Gi-MgO NPs) by extracting 6-gingerol (Gi) from Zingiber officinale rhizomes. The Gi-MgO NPs were further investigated for anticancer, anti-inflammatory, and antioxidant activities.
METHODS: The physical and chemical characteristics were examined by FT-IR, HPTLC, XRD, XPS, HR-SEM, HR-TEM, EDX, and zeta potential. Proton (1H) and carbon (13C) NMR spectroscopy were used to further understand the 6-gingerol compound. Gi-MgO NPs had well-dispersed spherical shapes with an average diameter of 26.18 ± 5.3 nm, a zeta potential of -16.82 ± 7.47 mV, and a polydispersity index (PDI) of 0.305, respectively. Following that, the human acute monocytic leukemia cell line (THP-1), anti-inflammatory action, and anti-oxidant properties were used to test the Gi-MgO NPs effects.
RESULTS: The Gi-loaded nanoparticles were shown to be more effective than 6-gingerol, as evidenced by their increased toxicity against the THP-1 cell line (IC50 of 16.48 μg/mL) relative to control cells. Additionally, NPs demonstrated notable anti-inflammatory action with a membrane stabilization method value of 76.41% at 100 μg/mL. Subsequently, the DPPH and ABTS antioxidant properties of NPs showed significant inhibition rates of 69.82% and 78.16%, respectively.
CONCLUSION: The present investigation revealed Gi-MgO NPs significant anticancer effect and ability to cause apoptosis in malignant cells by modifying the expression of apoptosis-related genes; however, additional ex vivo and molecular mechanism studies are required.
METHODS: The physical and chemical characteristics were examined by FT-IR, HPTLC, XRD, XPS, HR-SEM, HR-TEM, EDX, and zeta potential. Proton (1H) and carbon (13C) NMR spectroscopy were used to further understand the 6-gingerol compound. Gi-MgO NPs had well-dispersed spherical shapes with an average diameter of 26.18 ± 5.3 nm, a zeta potential of -16.82 ± 7.47 mV, and a polydispersity index (PDI) of 0.305, respectively. Following that, the human acute monocytic leukemia cell line (THP-1), anti-inflammatory action, and anti-oxidant properties were used to test the Gi-MgO NPs effects.
RESULTS: The Gi-loaded nanoparticles were shown to be more effective than 6-gingerol, as evidenced by their increased toxicity against the THP-1 cell line (IC50 of 16.48 μg/mL) relative to control cells. Additionally, NPs demonstrated notable anti-inflammatory action with a membrane stabilization method value of 76.41% at 100 μg/mL. Subsequently, the DPPH and ABTS antioxidant properties of NPs showed significant inhibition rates of 69.82% and 78.16%, respectively.
CONCLUSION: The present investigation revealed Gi-MgO NPs significant anticancer effect and ability to cause apoptosis in malignant cells by modifying the expression of apoptosis-related genes; however, additional ex vivo and molecular mechanism studies are required.