TY - JOUR
T1 - Self-evolved hydrogen peroxide boosts photothermal-promoted tumor-specific nanocatalytic therapy
AU - Gao, Shanshan
AU - Lu, Xiangyu
AU - Zhu, Piao
AU - Lin, Han
AU - Yu, Luodan
AU - Yao, Heliang
AU - Wei, Chenyang
AU - Chen, Yu
AU - Shi, Jianlin
N1 - Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - The emerging nanocatalytic tumor therapy such as chemodynamic therapy (CDT) converts less harmful hydrogen peroxide (H2O2) into highly toxic hydroxyl radicals (OH) via metal ion-mediated catalytic Fenton chemistry, which has motivated extensive research interest due to the high specificity of the nanocatalytic reactions to the tumor microenvironment (TME) and minimized side effects. However, traditional CDT substantially suffers from the insufficiency of intratumoral H2O2 for inducing a satisfactory therapeutic efficacy. In this work, we report on a photothermally-promoted Fenton reaction triggered by self-supplied H2O2, based on the constructed two-dimensional (2D) multifunctional therapeutic Nb2C-IO-CaO2 nanoreactors with enhanced therapeutic efficacy and therapeutic biosafety. These Nb2C-IO-CaO2 nanoreactors employ calcium peroxide (CaO2) as a potent H2O2 supplier to sustain the iron oxide (IO) nanoparticle-mediated catalytic Fenton reaction, and to liberate highly toxic OH for inducing tumor-cell apoptosis. Meanwhile, the intratumoral OH production was further promoted by the photothermal effect of the Nb2C-IO-CaO2 nanoreactors under near infrared irradiation at the second biowindow. Extensive in vitro and in vivo evaluations have demonstrated significantly enhanced reactive oxygen species (ROS) production and an outstanding photothermal effect based on these Nb2C-IO-CaO2 nanoreactors, which synergistically lead to elevated therapeutic efficacy. Therefore, this work not only exhibits a promising prospect for reforming the TME to achieve enhanced Fenton reactivity for CDT by elaborately designed nanomaterials with multifunctionality, but also provides novel efficient cancer-therapeutic modalities with simultaneous high therapeutic efficacy and low side effects.
AB - The emerging nanocatalytic tumor therapy such as chemodynamic therapy (CDT) converts less harmful hydrogen peroxide (H2O2) into highly toxic hydroxyl radicals (OH) via metal ion-mediated catalytic Fenton chemistry, which has motivated extensive research interest due to the high specificity of the nanocatalytic reactions to the tumor microenvironment (TME) and minimized side effects. However, traditional CDT substantially suffers from the insufficiency of intratumoral H2O2 for inducing a satisfactory therapeutic efficacy. In this work, we report on a photothermally-promoted Fenton reaction triggered by self-supplied H2O2, based on the constructed two-dimensional (2D) multifunctional therapeutic Nb2C-IO-CaO2 nanoreactors with enhanced therapeutic efficacy and therapeutic biosafety. These Nb2C-IO-CaO2 nanoreactors employ calcium peroxide (CaO2) as a potent H2O2 supplier to sustain the iron oxide (IO) nanoparticle-mediated catalytic Fenton reaction, and to liberate highly toxic OH for inducing tumor-cell apoptosis. Meanwhile, the intratumoral OH production was further promoted by the photothermal effect of the Nb2C-IO-CaO2 nanoreactors under near infrared irradiation at the second biowindow. Extensive in vitro and in vivo evaluations have demonstrated significantly enhanced reactive oxygen species (ROS) production and an outstanding photothermal effect based on these Nb2C-IO-CaO2 nanoreactors, which synergistically lead to elevated therapeutic efficacy. Therefore, this work not only exhibits a promising prospect for reforming the TME to achieve enhanced Fenton reactivity for CDT by elaborately designed nanomaterials with multifunctionality, but also provides novel efficient cancer-therapeutic modalities with simultaneous high therapeutic efficacy and low side effects.
UR - https://www.scopus.com/pages/publications/85066855356
U2 - 10.1039/c9tb00525k
DO - 10.1039/c9tb00525k
M3 - 文章
AN - SCOPUS:85066855356
SN - 2050-750X
VL - 7
SP - 3599
EP - 3609
JO - Journal of Materials Chemistry B
JF - Journal of Materials Chemistry B
IS - 22
ER -