Chitosan loaded copper and selenium nanoparticles synergistically inhibit HepG2-hepatic cancer cells viability and angiogenesis.

Key Points

• This research examines the effects of chitosan loaded copper and selenium nanoparticles on hepatic cancer cells.
• Evaluated the impact of nanoparticles on HepG2 cell viability
• Assessed anti-angiogenic effects in vitro
• Measured changes in cell viability and angiogenesis
• Demonstrated significant reduction in HepG2 cell viability
• Showed decreased angiogenesis linked to nanoparticles
• Highlighted the dual functionality as cytotoxic and anti-angiogenic agents

Abstract