Current chemodynamic therapy (CDT) primarily relies on the delivery of transition metal ions
with Fenton activity to trigger hydroxyl radical production from hydrogen peroxide. However …

Chemodynamic therapy (CDT) utilizes iron‐initiated Fenton chemistry to destroy tumor cells
by converting endogenous H2O2 into the highly toxic hydroxyl radical (. OH). There is a …

Amplifying intracellular oxidative stress effectively destroys cancer cells. In addition, iron-
mediated Fenton reaction converts endogenous H2O2 to produce hypertoxic hydroxyl …

Cancer cells, compared to normal cells, are under oxidative stress associated with an
elevated level of reactive oxygen species (ROS) and are more vulnerable to oxidative stress …

Recently, nanoparticle‐triggered in situ catalytic Fenton/Fenton‐like reaction is widely
explored for tumor‐specific chemodynamic therapy (CDT). However, despite the great …

Tailored to the specific tumour microenvironment, which involves acidity and the
overproduction of hydrogen peroxide, advanced nanotechnology has been introduced to …

In view of certain unique internalization features of the tumor microenvironment
(TME)(mainly including hypoxia, acidity and higher concentrations of H 2 O 2 and GSH) …

Amplification of intracellular oxidative stress has been found to be an effective strategy to
induce cancer cell death. To this end, we prepare a unique type of ultrasmall gallic acid …

Chemodynamic therapy (CDT), defined as an in situ oxidative stress response catalyzed by
the Fenton or Fenton-like reactions to generate cytotoxic hydroxyl radicals (• OH) at tumor …

Reactive oxygen species (ROS)‐induced apoptosis is a widely practiced strategy for cancer
therapy. Although photodynamic therapy (PDT) takes advantage of the spatial–temporal …