| Literature DB >> 30548916 |
Heqi Gao1, Pingping Bao2, Shuxin Dai1, Ruihua Liu1, Shenglu Ji1, Sheng Zeng3, Jing Shen2, Qian Liu3, Dan Ding1,4.
Abstract
Despite of the enthusiastic research in aggregation-induced emission luminogens (AIEgens) in recent years, the ones that can be smoothly used for sophisticated biomedical applications such as in vivo bioimaging of pulmonary metastatic tumors during surgery are still limited. Herein, we report the design and synthesis of a new series of far-red/near-infrared (FR/NIR) fluorescent AIEgens that consist of methoxy-substituted tetraphenylethene (TPE) as the electron-donating moiety, (1,3-dimethyl)barbituric acid as the electron-withdrawing moiety, and different π-bridge units. As compared to benzene or 3,4-ethylenedioxythiophene, using thiophene as the π-conjugation unit between the donor and acceptor results in a relatively higher absolute fluorescence quantum yield (14.5 %) in water when formulating the corresponding AIEgens into nanoparticles (AIE dots) with an amphiphilic co-polymer as the doping matrix. The highly FR/NIR-emissive thiophene-based AIE dots are demonstrated to be potent for intraoperative detection of pulmonary metastatic tumors, particularly the micro-sized ones, with excellent signal-to-background ratio.Entities:
Keywords: aggregation-induced emission; barbituric acid; fluorescence imaging; image-guided cancer surgery; luminogens
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Year: 2018 PMID: 30548916 DOI: 10.1002/asia.201801660
Source DB: PubMed Journal: Chem Asian J ISSN: 1861-471X