Ouyang Zi, Liu Bo, Yasmin-Karim Sayeda, Sajo Erno, Ngwa Wilfred
Department of Radiation Oncology, Brigham and Women's Hospital, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA; Medical Physics Program, Department of Physics and Applied Physics, University of Massachusetts Lowell, Lowell, MA, USA.
Medical Physics Program, Department of Physics and Applied Physics, University of Massachusetts Lowell, Lowell, MA, USA.
Phys Med. 2016 Jul;32(7):944-7. doi: 10.1016/j.ejmp.2016.06.015. Epub 2016 Jul 5.
This study investigates the feasibility of exploiting the Čerenkov radiation (CR) present during external beam radiotherapy (EBRT) for significant therapeutic gain, using titanium dioxide (titania) nanoparticles (NPs) delivered via newly designed radiotherapy biomaterials. Using Monte Carlo radiation transport simulations, we calculated the total CR yield inside a tumor volume during EBRT compared to that of the radionuclides. We also considered a novel approach for intratumoral titania delivery using radiotherapy biomaterials (e.g. fiducials) loaded with NPs. The intratumoral distribution/diffusion of titania released from the fiducials was calculated. To confirm the CR induced enhancement in EBRT experimentally, we used 6MV radiation to irradiate human lung cancer cells with or without titania NPs and performed clonogenic assays. For a radiotherapy biomaterial loaded with 20μg/g of 2-nm titania NPs, at least 1μg/g could be delivered throughout a tumor sub-volume of 2-cm diameter after 14days. This concentration level could inflict substantial damage to cancer cells during EBRT. The Monte Carlo results showed the CR yield by 6MV radiation was higher than by the radionuclides of interest and hence greater damage might be obtained during EBRT. In vitro study showed significant enhancement with 6MV radiation and titania NPs. These preliminary findings demonstrate a potential new approach that can be used to take advantage of the CR present during megavoltage EBRT to boost damage to cancer cells. The results provide significant impetus for further experimental studies towards the development of nanoparticle-aided EBRT powered by the Čerenkov effect.
本研究探讨了利用外照射放射治疗(EBRT)过程中产生的切伦科夫辐射(CR)实现显著治疗增益的可行性,方法是通过新设计的放射治疗生物材料递送二氧化钛(二氧化钛)纳米颗粒(NPs)。利用蒙特卡罗辐射传输模拟,我们计算了EBRT期间肿瘤体积内的总CR产量,并与放射性核素的产量进行了比较。我们还考虑了一种使用负载NPs的放射治疗生物材料(如基准标记物)进行瘤内二氧化钛递送的新方法。计算了从基准标记物释放的二氧化钛在瘤内的分布/扩散情况。为了通过实验证实EBRT中CR诱导的增强作用,我们使用6MV辐射照射有或没有二氧化钛NPs的人肺癌细胞,并进行了克隆形成试验。对于负载20μg/g 2纳米二氧化钛NPs的放射治疗生物材料,14天后至少1μg/g可以递送至直径为2厘米的肿瘤子体积内。该浓度水平在EBRT期间可能对癌细胞造成实质性损伤。蒙特卡罗结果表明,6MV辐射产生的CR产量高于相关放射性核素,因此在EBRT期间可能会造成更大的损伤。体外研究表明,6MV辐射和二氧化钛NPs具有显著的增强作用。这些初步发现证明了一种潜在的新方法,可用于利用兆伏EBRT期间存在的CR来增强对癌细胞的损伤。这些结果为进一步开展基于切伦科夫效应的纳米颗粒辅助EBRT开发的实验研究提供了重要动力。