This research aims to develop a novel nanoparticle platform to enhance photodynamic therapy for cervical cancer by addressing tumor hypoxia.
Development of NIR-activated IFHFC nanoparticles
Utilization of dual-mode oxygenation techniques including CAT-catalyzed oxygen generation and PFH oxygen release
Implementation of NIR-I/NIR-II imaging for monitoring efficacy
Enhanced oxygen delivery to tumor sites alleviates hypoxia
Increased production of reactive oxygen species (ROS) promotes more effective photodynamic therapy
Improved imaging capabilities aid in assessing treatment response
Resumen
NIR-activated IFHFC nanoparticles enable NIR-I/NIR-II imaging and dual oxygenation (CAT-catalyzed O 2 generation and PFH O 2 release), relieving hypoxia and boosting ROS for enhanced PDT.