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Room-temperature phosphorescence of defect-engineered silica nanoparticles for high-contrast afterglow bioimaging

Authors
Chang, HeeminPark, YoonsangKim, KyunghwanHan, ChaewonYoon, YeongjunYoo, WoojungYoo, JounghyunLee, DajinHan, HyunhoKim, KyeounghakJoo, JinmyoungKwon, Woosung
Issue Date
Aug-2024
Publisher
Elsevier B.V.
Keywords
Defect engineering; Room-temperature phosphorescence; Silica nanoparticle; Time-gated imaging; Tumor-targeting nanomedicine
Citation
Chemical Engineering Journal, v.493
Journal Title
Chemical Engineering Journal
Volume
493
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/160224
DOI
10.1016/j.cej.2024.152529
ISSN
1385-8947
1873-3212
Abstract
Room-temperature phosphorescence (RTP) has tremendous potential in optics and photonics. Unlike fluorescence, RTP has substantial afterglow signals even after the excitation light is removed, which allows for extended acquisition times and higher signal-to-noise ratio under time-gated bioimaging. However, conventional RTP materials, both metal-containing and metal-free organic compounds, typically have limited photostability and inherent toxicity, making them unsuitable for long-term biological applications. Here, we report metal- and organic fluorophore-free silica nanoparticles (SNPs) that facilitate long-lived phosphorescence and exhibit RTP for high-contrast bioimaging. Polycondensation of silicon precursors and silyl biphenyls forms biphenyl-doped SNPs (bSNPs), and thermal decomposition of biphenyl moieties generates optically active defects in the biphenyl-bonded silicate network. The calcined bSNPs (C-bSNPs) have RTP-related biphenyl defects composed of carbon impurities, corresponding to spectroscopic measurements and ab initio calculations. Facile surface functionalization of defect-engineered C-bSNPs with tumor-targeting peptides while maintaining long-lived RTP allows for tissue autofluorescence-free in vivo bioimaging for cancer diagnosis, surpassing the limitations of continuous-wave imaging. © 2024
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