Albumin-based nanosystem for dual-modality imaging-guided chem-phototherapy against immune-cold triple-negative breast cancer.
Chen PengXiaodie ZengJiali CaiHanyu HuangFan YangShaowen JinXiuhong GuanZhi-Yong WangPublished in: Regenerative biomaterials (2023)
Triple-negative breast cancer is a highly aggressive and metastatic tumor; diagnosing it in the early stages is still difficult, and the prognosis for conventional radio-chemotherapy and immunotreatment is not promising due to cancer's immunosuppressive microenvironment. The utilization of protein-based nanosystem has proven to be effective in delivering agents with limited adverse effects, yet the combination of diagnosis and treatment remains a difficult challenge. This research took advantage of natural albumin and organic molecules to construct a self-assemble core-shell nanostructure combining with superparamagnetic iron oxide nanocrystals and heptamethine cyanine dye IR780 through non-covalent interactions. This nanocomposite successfully decreased the transverse relaxation time of the magnetic resonance hydrogen nucleus, resulting in outstanding T 2 imaging, as well as emitting near-infrared II fluorescence, thereby the resulting dual-modality imaging tool was applied to improve diagnostic competency. It is noteworthy that the nanocomposites exhibited impressive enzyme-like catalytic and photothermal capabilities, resulting in a successful activation of the immune system to efficiently suppress distant metastatic lesions in vivo . Consequently, this nano-drug-based therapy could be an advantageous asset in reinforcing the immune system and hindering the growth and reappearance of the immune-cold breast cancer.
Keyphrases
- high resolution
- magnetic resonance
- iron oxide
- squamous cell carcinoma
- small cell lung cancer
- stem cells
- reduced graphene oxide
- energy transfer
- lymph node
- photodynamic therapy
- emergency department
- mesenchymal stem cells
- bone marrow
- highly efficient
- mass spectrometry
- young adults
- ionic liquid
- gold nanoparticles
- solid phase extraction
- liquid chromatography
- protein protein