4.8 Article

Highly Fluorescent Ribonuclease-A-Encapsulated Lead Sulfide Quantum Dots for Ultrasensitive Fluorescence in Vivo Imaging in the Second Near-Infrared Window

期刊

CHEMISTRY OF MATERIALS
卷 28, 期 9, 页码 3041-3050

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.6b00208

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资金

  1. University of Leeds
  2. Wellcome Trust (UK) [097354/Z/11/Z]
  3. University of Leeds (UK)
  4. Huashan Hospital (China)
  5. Royal Society-International Exchange Scheme (China NSFC cost-share)
  6. National 863 Hi-Tech Project [2015AA033703]
  7. National Natural Science Foundation of China [81271958, 81301672, 81401771, 81201773, 21171117]
  8. Natural Science Foundation of Shanghai Project [12ZR1415800, 15ZR1405000]
  9. Specialized Research Fund for the Doctoral Program of Higher Education [20120071110067]
  10. China Postdoctoral Science Foundation [2014M560296]
  11. Shanghai Municipal Education Commission [15ZZ006]
  12. Wellcome Trust [097354/Z/11/Z] Funding Source: Wellcome Trust
  13. EPSRC [EP/E015530/1, EP/K023845/1, EP/I000623/1] Funding Source: UKRI

向作者/读者索取更多资源

Ribonuclease-A (RNase-A) encapsulated PbS quantum dots (RNase-A@PbS Qdots) which emit in the second near-infrared biological window (NIR-II, ca. 1000-1400 nm) are rapidly synthesized under microwave heating. Photoluminescence (PL) spectra of the Qdots can be tuned across the entire NIR-II range by simply controlling synthesis temperature. The size and morphology of the Qdots are examined by transmission electron microscopy (TEM), atomic force microscopy (AFM), and dynamic light scattering (DLS). Quantum yield (Phi(f)) measurement confirms that the prepared Qdots are one of the brightest water-soluble NIR-II emitters for in vivo imaging. Their high Phi(f) (similar to 17.3%) and peak emission at 4300 nm ensure deep optical penetration to muscle tissues (up to 1.5 cm) and excellent imaging contrast at an extremely low threshold dose of similar to 5.2 pmol (similar to 1 mu g) per mouse. Importantly, this protein coated Qdot displays no signs of toxicity toward model neuron, normal, and cancer cells in vitro. In addition, the animal's metabolism results in thorough elimination of intravenously injected Qdots from the body within several days via the reticuloendothelial system (RES), which minimizes potential long-term toxicity in vivo from possible release of lead content. With a combination of attractive properties of high brightness, robust photostability, and excellent biocompatibility, this new NIR-II emitting Qdot is highly promising in accurate disease screening and diagnostic applications.

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