J Biomed Opt. 2012 Apr;17(4):040506. doi: 10.1117/1.JBO.17.4.040506.
In vivo Cerenkov luminescence imaging is a rapidly growing molecular imaging research field based on the detection of Cerenkov radiation induced by beta particles when traveling though biological tissues. We investigated theoretically the possibility of enhancing the number of the detected Cerenkov photons in the near infrared (NIR) region of the spectrum. The analysis is based on applying a photon propagation diffusion model to Cerenkov photons in the tissue. Results show that despite the smaller number of Cerenkov photons in the NIR region, the fraction exiting the tissues is greater than in the visible range, and thus, a charge-coupled device detector optimized for the NIR range will allow to obtain a higher signal. The comparison was performed considering Cerenkov point sources located at different depths inside the animal. We concluded that the improvement can be up to 35% and is more significant when the Cerenkov source to be imaged is located deeper inside the animal.
体内切伦科夫发光成像是一个快速发展的分子成像研究领域,基于检测β粒子在穿过生物组织时产生的切伦科夫辐射。我们从理论上研究了在光谱近红外(NIR)区域增强检测到的切伦科夫光子数量的可能性。该分析基于将光子传播扩散模型应用于组织中的切伦科夫光子。结果表明,尽管 NIR 区域的切伦科夫光子数量较少,但从组织中逸出的分数大于可见范围,因此,针对 NIR 范围优化的电荷耦合器件探测器将允许获得更高的信号。考虑到位于动物内部不同深度的切伦科夫点源进行了比较。我们得出的结论是,这种改进可以高达 35%,并且当要成像的切伦科夫源位于动物内部更深时,效果更为显著。