Activatable probes based on distance-dependent luminescence associated with Cerenkov radiation.
Activatable probes based on distance-dependent luminescence associated with Cerenkov radiation.
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DOI:
10.1002/anie.201302564
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发表时间:
2013-07-22
影响因子:
16.6
通讯作者:
Achilefu, Samuel
中科院分区:
文献类型:
--
作者:
Kotagiri, Nalinikanth;Niedzwiedzki, Dariusz M.;Ohara, Kohtaro;Achilefu, Samuel
Optical imaging techniques have evolved from basic preclinical to enabling clinical technology platform for the diagnosis and treatment of human diseases. A major bottleneck for the clinical translation of light based imaging and therapeutic techniques is the limited penetrability of light in deep tissue. This drawback has led to widespread attention and renewed interest in Cerenkov emission, especially in the area of molecular imaging, as a tissue depth-independent spontaneous light source.[1] Cerenkov radiation (CR) is a photophysical phenomenon where continuous wave (CW) light in the 250–600 nm range is emitted by charged particles such as positrons and electrons when travelling faster than light in a dielectric medium with refractive index> 1.[2] Generally, appreciable CR is produced as a ‘byproduct’of highly energetic radionuclide or external beam radiation that are used in various clinical interventions. However, due to significant tissue autofluorescence, absorption and scattering of UV and visible light, Cerenkov luminescence imaging (CLI) faces steep challenges such as rapid signal attenuation and low fluence rates. Thus, coupling CR with fluorophores that emit in the optical window at wavelengths between 650 nm and 950 nm will minimize tissue autofluorescence and enhance detection of light from deep tissue.
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