Highly Fluorescent Ribonuclease-A-Encapsulated Lead
Sulfide Quantum Dots for Ultrasensitive Fluorescence in Vivo Imaging in the Second Near-Infrared Window
posted on 2016-04-06, 00:00authored byYifei Kong, Jun Chen, Hongwei Fang, George Heath, Yan Wo, Weili Wang, Yunxia Li, Yuan Guo, Stephen
D. Evans, Shiyi Chen, Dejian Zhou
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 (Φf) measurement
confirms that the prepared Qdots are one of the brightest water-soluble
NIR-II emitters for in vivo imaging. Their high Φf (∼17.3%) and peak emission at ∼1300 nm ensure
deep optical penetration to muscle tissues (up to 1.5 cm) and excellent
imaging contrast at an extremely low threshold dose of ∼5.2
pmol (∼1 μg) 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.