The pH-controlled release properties of chitosan-gold nanoparticles encapsulated nobiletin to induce apoptosis through PI3K/AKT/mTOR signalling pathway on gastric cancer cell lines.
[CONTEXT] Gastric cancer (GC) remains a major health concern with limited effective therapies.
APA
Qing H, Xie P, et al. (2025). The pH-controlled release properties of chitosan-gold nanoparticles encapsulated nobiletin to induce apoptosis through PI3K/AKT/mTOR signalling pathway on gastric cancer cell lines.. Journal of microencapsulation, 42(6), 565-579. https://doi.org/10.1080/02652048.2025.2507638
MLA
Qing H, et al.. "The pH-controlled release properties of chitosan-gold nanoparticles encapsulated nobiletin to induce apoptosis through PI3K/AKT/mTOR signalling pathway on gastric cancer cell lines.." Journal of microencapsulation, vol. 42, no. 6, 2025, pp. 565-579.
PMID
40450390
Abstract
[CONTEXT] Gastric cancer (GC) remains a major health concern with limited effective therapies. Nanotechnology-based drug delivery systems offer targeted and efficient treatment strategies.
[OBJECTIVE] This study aimed to develop chitosan-coated gold nanoparticles loaded with Nobiletin (Ch-AuNPs-NB) and evaluate their anticancer potential by targeting the PI3K/AKT/mTOR signaling pathway in GC.Ch-AuNPs were synthesized by NaBH reduction and loaded with Nobiletin using nanoprecipitation. Characterization was done using UV-Vis, FTIR, XRD, DLS, and TEM. Drug loading, encapsulation efficiency, and pH-responsive release were assessed.
[RESULTS] Ch-AuNPs-NB (∼120 nm, PDI 0.247, +51 mV) showed enhanced drug loading (15%) and encapsulation efficiency (90.4%) at higher NB concentrations. The formulation demonstrated pH-responsive release over 72 hours and stability for 60 days.
[DISCUSSION AND CONCLUSION] Ch-AuNPs-NB inhibited the PI3K/AKT/mTOR pathway, induced apoptosis, and arrested the cell cycle in AGS cells, highlighting its potential as a targeted GC therapy.
[OBJECTIVE] This study aimed to develop chitosan-coated gold nanoparticles loaded with Nobiletin (Ch-AuNPs-NB) and evaluate their anticancer potential by targeting the PI3K/AKT/mTOR signaling pathway in GC.Ch-AuNPs were synthesized by NaBH reduction and loaded with Nobiletin using nanoprecipitation. Characterization was done using UV-Vis, FTIR, XRD, DLS, and TEM. Drug loading, encapsulation efficiency, and pH-responsive release were assessed.
[RESULTS] Ch-AuNPs-NB (∼120 nm, PDI 0.247, +51 mV) showed enhanced drug loading (15%) and encapsulation efficiency (90.4%) at higher NB concentrations. The formulation demonstrated pH-responsive release over 72 hours and stability for 60 days.
[DISCUSSION AND CONCLUSION] Ch-AuNPs-NB inhibited the PI3K/AKT/mTOR pathway, induced apoptosis, and arrested the cell cycle in AGS cells, highlighting its potential as a targeted GC therapy.
MeSH Terms
Humans; Chitosan; Gold; TOR Serine-Threonine Kinases; Apoptosis; Proto-Oncogene Proteins c-akt; Metal Nanoparticles; Flavones; Stomach Neoplasms; Hydrogen-Ion Concentration; Phosphatidylinositol 3-Kinases; Signal Transduction; Cell Line, Tumor; Delayed-Action Preparations; Drug Liberation; Antineoplastic Agents