Highly efficient delivery of nanoagents to the
tumor region remains the primary challenge for
cancer nanomedicine. Herein, we propose a NO-mediated tumor microenvironment (TME) remodeling strategy for the high-efficient delivery of nanoagents into
tumor.
Quantum dots (QDs) with bright fluorescence in the near-infrared IIb (NIR-IIb, 1500-1700 nm) window and high photothermal conversion efficiency were encapsulated into
liposomes for the imaging-guided
photothermal therapy (PTT) of
tumor. The fabrication of PEG and
arginine-
glycine-
aspartate (
RGD) peptide on
liposomes ensured the prolonged circulation in vivo and active targeting to
tumor. Moreover, the loading of a natural NO generator
L-arginine in
liposomes realized the continuous generation of NO in the acidic TME. By co-localization fluorescence imaging and western blot of
tumor tissue, we confirmed that the release of NO activated the expression of
metalloproteinases in TME and further degraded
Collagen I in the peripheral region of the
tumor, thus removing the barrier for the permeation of
liposomes. Attributed to the enhanced accumulation of
liposomes inside the
tumor, NIR IIb imaging-guided PTT was achieved with remarkable therapeutic efficacy.