In vivo real-time and in situ sensing of nitric oxide in virus-infected mouse lungs using organic near-infrared-to-visible triplet–triplet annihilation upconversion nanoprobes
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引用次数: 0
Abstract
Nitric oxide (NO) is a crucial gaseous signaling molecule, and its local concentration fluctuations in vivo can reflect the onset and progression of various pulmonary diseases, such as idiopathic pulmonary fibrosis and viral lung infections. Previous studies have demonstrated a positive correlation between in vivo NO concentration and disease progression, highlighting the urgent need to develop a class of bioprobes capable of highly sensitive and specific real-time NO sensing within living organisms. Herein, we report a “turn-on” near-infrared fluorescence sensing nanoprobe for nitric oxide (NO), which integrates a near-infrared-to-visible triplet–triplet annihilation upconversion (TTA-UC) system with an NO-responsive Bodipy dye. By co-encapsulating both components into the amphiphilic polymer F127, we constructed TTA micelles with excellent photostability and biocompatibility. In vitro studies demonstrated that the TTA nanomicelles can sensitively and specifically respond to exogenous NO. In a pseudotyped mouse model of pulmonary viral infection induced by SARS-CoV-2 spike protein (SP), the upconversion fluorescence of the TTA nmicelles was gradually activated over time, indicating that the developed nanoprobe can dynamically reflect the real-time progression of lung infection in mice. Therefore, the TTA micelles can rapidly diagnose the onset of lung infection at early stages, thereby potentially improving the efficiency of subsequent treatments.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.