Lighting up Self-Quenching Nanoaggregates with Protein Corona for Simultaneous Intraoperative Imaging and Photothermal Theranostics of Metastatic Cancer.
Xueluer MuWenbi FengChunfeng LiKaixuan LiYajie LiXue JingYingxi LuXianfeng ZhouZhibo LiPublished in: Analytical chemistry (2022)
Near-infrared (NIR) photothermal transduction agents (PTAs) with large rigid π-extended and planar structures are prone to aggregate in a physiological environment where their emission is often quenched due to the strong intermolecular dipole-dipole or π-π interactions. This aggregation-caused quenching effect greatly impedes their applications in image-guided photothermal theranostics. Herein, we made an interesting finding that engineering a bioinspired protein corona (PC), once thermodynamically stabilized in preferred orientations on PTA nanoaggregates, can produce brilliant NIR fluorescence with a high quantum yield (∼6.2%) without compromising their photothermal properties. Both experimental data and computational modeling suggest that the mechanism of fluorescence enhancement is due to the high-affinity binding of nano-sized PTA to albumin, which regulates the molecular conformation and aggregation state of PTA. High spatial and temporal resolution imaging of albumin PC-coated PTA aggregates enables image-guided photothermal therapy for cancer cells in sentinel lymph nodes to remarkably inhibit pulmonary metastasis. Such a treatment combined with the surgical removal of the primary tumor can prolong animal survival, which is a promising candidate for clinical applications in the treatment of advanced metastatic cancers.
Keyphrases
- photodynamic therapy
- drug release
- cancer therapy
- energy transfer
- drug delivery
- fluorescence imaging
- high resolution
- lymph node
- single molecule
- squamous cell carcinoma
- small cell lung cancer
- binding protein
- pulmonary hypertension
- molecular dynamics
- papillary thyroid
- protein protein
- squamous cell
- young adults
- dna binding
- data analysis