Tumor penetration of nanocarriers is still an unresolved challenge for effective drug delivery. Herein, we described a size-switchable nanoplatform in response to an external near-infrared (NIR) laser for transcellular drug delivery. The nanoplatform was constructed with a poly( N -isopropylacrylamide) (PNIPAM)-based nanogel encapsulating chitosan-coated single-walled carbon nanotubes, followed by loading a chemotherapeutic drug, doxorubicin (DOX). In mice bearing orthotopic breast tumors, the photothermal effect from single-walled carbon nanotubes upon NIR irradiation potently inhibited tumor growth. The antitumor effect of the nanomedicine with NIR irradiation might be attributed to its capability of transcellular transport and tumor penetration in mice. In addition, the nanomedicine with NIR irradiation could elicit an antitumor response by increasing cytotoxic T cells and decreasing myeloid-derived suppressor cells. These results validated the application of photo/thermo-responsive nanomedicine in the orthotopic model of breast cancer.
Keyphrases
- cancer therapy
- drug delivery
- drug release
- walled carbon nanotubes
- photodynamic therapy
- fluorescent probe
- high fat diet induced
- fluorescence imaging
- induced apoptosis
- radiation induced
- cell cycle arrest
- emergency department
- type diabetes
- cell death
- adipose tissue
- mass spectrometry
- wild type
- young adults
- electron transfer
- cell proliferation
- combination therapy
- wound healing
- childhood cancer