Highly Twisted Conformation Thiopyrylium Photosensitizers for In Vivo Near Infrared-II Imaging and Rapid Inactivation of Coronavirus.
Yishen LiuMeijia GuQihang DingZhiyun ZhangWanxia GongYuncong YuanXiaofei MiaoHuili MaXuechuan HongWenbo HuYuling XiaoPublished in: Angewandte Chemie (International ed. in English) (2022)
Despite significant effort, a majority of heavy-atom-free photosensitizers have short excitation wavelengths, thereby hampering their biomedical applications. Here, we present a facile approach for developing efficient near-infrared (NIR) heavy-atom-free photosensitizers. Based on a series of thiopyrylium-based NIR-II (1000-1700 nm) dyads, we found that the star dyad HD with a sterically bulky and electron-rich moiety exhibited configuration torsion and significantly enhanced intersystem crossing (ISC) compared to the parent dyad. The electron excitation characteristics of HD changed from local excitation (LE) to charge transfer (CT)-domain, contributing to a ≈6-fold reduction in energy gap (ΔE ST ), a ≈10-fold accelerated ISC process, and a ≈31.49-fold elevated reactive oxygen species (ROS) quantum yield. The optimized SP@HD-PEG 2K lung-targeting dots enabled real-time NIR-II lung imaging, which precisely guided rapid pulmonary coronavirus inactivation.
Keyphrases
- photodynamic therapy
- fluorescence imaging
- reactive oxygen species
- energy transfer
- molecular dynamics
- sars cov
- high resolution
- fluorescent probe
- electron transfer
- computed tomography
- drug delivery
- cell death
- dna damage
- quantum dots
- pulmonary hypertension
- cancer therapy
- image quality
- magnetic resonance imaging
- drug release
- loop mediated isothermal amplification
- dual energy
- positron emission tomography
- highly efficient
- coronavirus disease
- reduced graphene oxide
- sensitive detection
- electron microscopy
- visible light