A black phosphorus/manganese dioxide nanoplatform: Oxygen self-supply monitoring, photodynamic therapy enhancement and feedback.
basic_science · Level V
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- Record sourced from PubMed, PMID 30453214.
- Also identified by DOI 10.1016/j.biomaterials.2018.10.018.
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Abstract
Selecting the timing of laser treatment is an important task for improving O<sub>2</sub>-dependent photodynamic therapy (PDT) efficiency. Here, a black phosphorus-based strategy was developed for dual-mode monitoring oxygen self-supply, enhancing photodynamic therapy, and feeding back therapeutic effect. The hybridized nanoplatform (R-MnO<sub>2</sub>-FBP) was prepared by assembly of Rhodamine B (RhB)-encapsulated manganese dioxide (R-MnO<sub>2</sub>) as O<sub>2</sub> supplier and indicator, and fluorescein isothiocyanate (FITC)-labelled peptide-functionalized black phosphorus as the theranostic agent. The time-dependent assays suggested that the O<sub>2</sub> release was proportional to the liberation of Mn<sup>2+</sup> and RhB in the R-MnO<sub>2</sub>-FBP system. After specific delivery into cancer cells, R-MnO<sub>2</sub>-FBP was dissociated in the acidic and H<sub>2</sub>O<sub>2</sub>-rich environment and generated oxygen to overcome hypoxia-associated PDT resistance. In the meantime, it released both Mn<sup>2+</sup>and RhB dye, leading to dual-mode (magnetic resonance imaging/fluorescence imaging) monitoring of the oxygen self-supply process. More significantly, the imaging-guided PDT in hypoxic cells displayed 51.6% of cell apoptosis at optimizing timing of laser application, which could also be confirmed by the FITC fluorescence recovery induced by the activated caspase-3 in apoptotic cells. In vivo photonic therapy by R-MnO<sub>2</sub>-FBP further demonstrated the ability of R-MnO<sub>2</sub>-FBP to choose the timing of laser application, providing an efficient approach for the enhancement of PDT process.
Medical subject headings
- Manganese Compounds
- Neoplasms
- Oxides
- Oxygen
- Phosphorus
- Photosensitizing Agents