Related Experiment Video
Updated: Jan 8, 2026

An Integrated System to Remotely Trigger Intracellular Signal Transduction by Upconversion Nanoparticle-mediated Kinase Photoactivation
Published on: August 30, 2017
NIR-II Photocatalytic-Triggered Pyroptosis via Built-In Electric Field-Enhanced Reactive Oxygen Species Generation in
Changyu Cao1, Wenjia Xu2, Dapeng Chen1
1State Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), School of Flexible Electronics (Future Technologies), and School of Chemistry and Molecular Engineering, Nanjing Tech University (NanjingTech), Nanjing 211816, China.
Abstract:
Hypoxia-induced therapeutic resistance remains a major challenge for reactive oxygen species (ROS)-mediated pyroptotic cancer therapy. To overcome this limitation, we developed Au-Cu2O nanodumbbells (NDs) with photoresponsive built-in electric fields (BIEFs) via heterointerface engineering. This design enables oxygen-independent photocatalytic therapy under second near-infrared (NIR-II, 1064 nm) laser activation. The primary BIEF suppresses rapid recombination of photoexcited electron-hole (e--h+) pairs and promotes hot-electron transfer upon 1064 nm laser excitation. Meanwhile, a secondary photoinduced BIEF, arising from dynamic interfacial charge redistribution, further enhances directional charge separation and significantly improves catalytic activity. This dual modulation of electric fields enables sustained production of superoxide (·O2-) and hydroxyl radicals (·OH) via direct electron transfer and Cu+-mediated Fenton-like reactions, thereby maintaining ROS generation even under hypoxic conditions. The elevated ROS levels efficiently activate pyroptotic signaling pathways, leading to cell membrane rupture and pro-inflammatory immune responses in tumor cells. Combined with NIR-II photoacoustic (PA) imaging, this theranostic system enables spatiotemporally precise and hypoxia-tolerant cancer therapy with minimal off-target toxicity.

