Ultrafast fluorescence imaging in vivo with conjugated polymer fluorophores in the second near-infrared window

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作者
Guosong Hong
Yingping Zou
Alexander L. Antaris
Shuo Diao
Di Wu
Kai Cheng
Xiaodong Zhang
Changxin Chen
Bo Liu
Yuehui He
Justin Z. Wu
Jun Yuan
Bo Zhang
Zhimin Tao
Chihiro Fukunaga
Hongjie Dai
机构
[1] Stanford University,Department of Chemistry
[2] College of Chemistry and Chemical Engineering,Department of Radiology and Bio
[3] Central South University,X Program
[4] State Key Laboratory for Powder Metallurgy,undefined
[5] Central South University,undefined
[6] Institute of Super-microstructure and Ultrafast Process in Advanced Materials,undefined
[7] School of Physics and Electronics,undefined
[8] Central South University,undefined
[9] School of Medicine,undefined
[10] Stanford University,undefined
来源
Nature Communications | / 5卷
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摘要
In vivo fluorescence imaging in the second near-infrared window (1.0–1.7 μm) can afford deep tissue penetration and high spatial resolution, owing to the reduced scattering of long-wavelength photons. Here we synthesize a series of low-bandgap donor/acceptor copolymers with tunable emission wavelengths of 1,050–1,350 nm in this window. Non-covalent functionalization with phospholipid–polyethylene glycol results in water-soluble and biocompatible polymeric nanoparticles, allowing for live cell molecular imaging at >1,000 nm with polymer fluorophores for the first time. Importantly, the high quantum yield of the polymer allows for in vivo, deep-tissue and ultrafast imaging of mouse arterial blood flow with an unprecedented frame rate of >25 frames per second. The high time-resolution results in spatially and time resolved imaging of the blood flow pattern in cardiogram waveform over a single cardiac cycle (~200 ms) of a mouse, which has not been observed with fluorescence imaging in this window before.
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