Magnesium Oxide Nanoparticles Loaded with 6-Gingerol: A Bioinspired Approach to Anticancer, Anti-Inflammatory, and Antioxidant Therapy.
[PURPOSE] The aim of this work is to synthesize magnesium oxide nanoparticles (Gi-MgO NPs) by extracting 6-gingerol (Gi) from rhizomes.
APA
Kamaraj C, Yanto DHY, et al. (2026). Magnesium Oxide Nanoparticles Loaded with 6-Gingerol: A Bioinspired Approach to Anticancer, Anti-Inflammatory, and Antioxidant Therapy.. International journal of nanomedicine, 21, 531933. https://doi.org/10.2147/IJN.S531933
MLA
Kamaraj C, et al.. "Magnesium Oxide Nanoparticles Loaded with 6-Gingerol: A Bioinspired Approach to Anticancer, Anti-Inflammatory, and Antioxidant Therapy.." International journal of nanomedicine, vol. 21, 2026, pp. 531933.
PMID
41836722
Abstract
[PURPOSE] The aim of this work is to synthesize magnesium oxide nanoparticles (Gi-MgO NPs) by extracting 6-gingerol (Gi) from 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 (H) and carbon (C) 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 (IC 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 (H) and carbon (C) 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 (IC 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.
MeSH Terms
Catechols; Fatty Alcohols; Humans; Antioxidants; Anti-Inflammatory Agents; Zingiber officinale; Antineoplastic Agents; Magnesium Oxide; Nanoparticles; THP-1 Cells; Particle Size; Cell Survival; Cell Line, Tumor; Rhizome