Abstract
Alzheimer’s disease (AD) is a progressive neurodegenerative disorder for which the amyloid-beta (Aβ) deposit is widely recognized as a defining hallmark. Therefore, the development of robust probes capable of monitoring the aberrant aggregation and fibrillization of central Aβ aggregates is of paramount importance. However, conventional fluorescence-based assays for Aβ aggregates imaging are hampered by background interference and low specificity. Herein, we report a facile approach for the construction of organic room-temperature phosphorescence (RTP) nanoparticles through a host–guest doping strategy. The rationally engineered nanoparticles exhibit near-infrared emission (650–800 nm) and a prolonged phosphorescence lifetime (109 μs) and demonstrate exceptional blood–brain barrier permeability coupled with precise targeting of Aβ aggregates. Their unique optical and biological properties enable highly sensitive and time-resolved imaging of Aβ deposits, effectively enhancing the signal-to-noise ratios. Furthermore, the nanoparticles inhibit Aβ fibrillization and mitigate associated neurotoxicity in vitro, underscoring their theranostic potential for AD.
| Original language | English |
|---|---|
| Pages (from-to) | 14594-14601 |
| Number of pages | 8 |
| Journal | Analytical Chemistry |
| Volume | 97 |
| Issue number | 27 |
| DOIs | |
| State | Published - 15 Jul 2025 |
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