| Literature DB >> 27704754 |
Hua He1, Zhencai Wang1, Tiantian Cheng1, Xu Liu1, Xiaojuan Wang1, Junying Wang2, Hao Ren1, Yawei Sun1, Yanzhuo Song1, Jiang Yang3, Yongqing Xia1, Shengjie Wang1, Xiaodong Zhang2, Fang Huang1.
Abstract
Fluorescence imaging requires bioselective, sensitive, nontoxic molecular probes to detect the precise location of lesions for fundamental research and clinical applications. Typical inorganic semiconductor nanomaterials with large sizes (>10 nm) can offer high-quality fluorescence imaging due to their fascinating optical properties but are limited to low selectivity as well as slow clearance pathway. We here report an N- and O-rich carbogenic small molecular complex (SMC, MW < 1000 Da) that exhibits high quantum yield (up to 80%), nucleic acid-binding enhanced excitation-dependent fluorescence (EDF), and a near-infrared (NIR) emission peaked at 850 nm with an ultralarge Stokes shift (∼500 nm). SMCs show strong rRNA affinity, and the resulting EDF enhancement allows multicolor visualization of nucleoli in cells for clear statistics. Furthermore, SMCs can be efficiently accumulated in tumor in vivo after injection into tumor-bearing mice. The NIR emission affords high signal/noise ratio imaging for delineating the true extent of tumor. Importantly, about 80% of injected SMCs can be rapidly excreted from the body in 24 h. No appreciable toxicological responses were observed up to 30 days by hematological, biochemical, and pathological examinations. SMCs have great potential as a promising nucleolus- and tumor-specific agent for medical diagnoses and biomedical research.Entities:
Keywords: RNA selectivity; excitation-dependent fluorescence; small molecule; target-specific imaging; ultralarge Stokes shift
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Year: 2016 PMID: 27704754 DOI: 10.1021/acsami.6b10737
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229