TY - JOUR
T1 - Cytotoxicity and targeted drug delivery of green synthesized metallic nanoparticles against oral Cancer
T2 - A review
AU - M, Maghimaa
AU - Sagadevan, Suresh
AU - Suryadevara, Punna Rao
AU - Sudhan, Hari Hara
AU - Rao Burle, Gowri Sankara
AU - Ruokolainen, Janne
AU - Nelson, Vinod Kumar
AU - Kesari, Kavindra Kumar
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2025/3
Y1 - 2025/3
N2 - Recent advancements in nanotechnology have significantly contributed to developing innovative approaches in cancer therapy, particularly for oral cancer. This review focuses on the promising strategy of using green-synthesized metallic nanoparticles, which possess unique physicochemical properties suitable for targeted drug delivery and enhanced cytotoxicity against cancer cells. These Nanoparticles (NPs) are synthesized through environmentally friendly methods that utilize natural extracts or biomolecules as reducing and stabilizing agents. Their biocompatibility and capacity to penetrate biological barriers make them excellent for delivering therapeutic drugs directly to oral cancer cells, reducing systemic toxicity and increasing the efficacy of therapy. Numerous research on the cytotoxic effects of plant-synthesized Metallic Nanoparticles (MNPs) on oral cancer have demonstrated significant anticancer properties, attributable to their minute size and elevated surface-to-volume ratio. Functionalizing these nanoparticles with targeted ligands, such as peptides or antibodies allows for specific detection and binding to receptors that are overexpressed on cancer cell surfaces. This specific method improves cellular uptake of therapeutic medicines, resulting in enhanced apoptosis and suppression of tumor cell proliferation. Additionally, the tunability of the physicochemical properties of these nanoparticles allows for optimization of their therapeutic efficacy and pharmacokinetics. Overall, this review highlights that green-synthesized metallic nanoparticles can be used to develop targeted and successful diagnosis of the oral cancer treatment.
AB - Recent advancements in nanotechnology have significantly contributed to developing innovative approaches in cancer therapy, particularly for oral cancer. This review focuses on the promising strategy of using green-synthesized metallic nanoparticles, which possess unique physicochemical properties suitable for targeted drug delivery and enhanced cytotoxicity against cancer cells. These Nanoparticles (NPs) are synthesized through environmentally friendly methods that utilize natural extracts or biomolecules as reducing and stabilizing agents. Their biocompatibility and capacity to penetrate biological barriers make them excellent for delivering therapeutic drugs directly to oral cancer cells, reducing systemic toxicity and increasing the efficacy of therapy. Numerous research on the cytotoxic effects of plant-synthesized Metallic Nanoparticles (MNPs) on oral cancer have demonstrated significant anticancer properties, attributable to their minute size and elevated surface-to-volume ratio. Functionalizing these nanoparticles with targeted ligands, such as peptides or antibodies allows for specific detection and binding to receptors that are overexpressed on cancer cell surfaces. This specific method improves cellular uptake of therapeutic medicines, resulting in enhanced apoptosis and suppression of tumor cell proliferation. Additionally, the tunability of the physicochemical properties of these nanoparticles allows for optimization of their therapeutic efficacy and pharmacokinetics. Overall, this review highlights that green-synthesized metallic nanoparticles can be used to develop targeted and successful diagnosis of the oral cancer treatment.
KW - Bioactive compounds
KW - Drug delivery
KW - Metallic Nanoparticles
KW - Oral cancer
KW - Plant extract
UR - http://www.scopus.com/inward/record.url?scp=85214118186&partnerID=8YFLogxK
U2 - 10.1016/j.inoche.2024.113806
DO - 10.1016/j.inoche.2024.113806
M3 - Review Article
AN - SCOPUS:85214118186
SN - 1387-7003
VL - 173
JO - Inorganic Chemistry Communications
JF - Inorganic Chemistry Communications
M1 - 113806
ER -