Author:
Dong Yuxi C.,Hajfathalian Maryam,Maidment Portia S. N.,Hsu Jessica C.,Naha Pratap C.,Si-Mohamed Salim,Breuilly Marine,Kim Johoon,Chhour Peter,Douek Philippe,Litt Harold I.,Cormode David P.
Abstract
Abstract
Computed tomography (CT) is one of the most commonly used clinical imaging modalities. There have recently been many reports of novel contrast agents for CT imaging. In particular, the development of gold nanoparticles (AuNP) as CT contrast agents is a topic of intense interest. AuNP have favorable characteristics for this application such as high payloads of contrast generating material, strong X-ray attenuation, excellent biocompatibility, tailorable surface chemistry, and tunable sizes and shapes. However, there have been conflicting reports on the role of AuNP size on their contrast generation for CT. We therefore sought to extensively investigate the AuNP size-CT contrast relationship. In order to do this, we synthesized AuNP with sizes ranging from 4 to 152 nm and capped them with 5 kDa m-PEG. The contrast generation of AuNP of different sizes was investigated with three clinical CT, a spectral photon counting CT (SPCCT) and two micro CT systems. X-ray attenuation was quantified as attenuation rate in Hounsfield units per unit concentration (HU/mM). No statistically significant difference in CT contrast generation was found among different AuNP sizes via phantom imaging with any of the systems tested. Furthermore, in vivo imaging was performed in mice to provide insight into the effect of AuNP size on animal biodistribution at CT dose levels, which has not previously been explored. Both in vivo imaging and ex vivo analysis with inductively coupled plasma optical emission spectroscopy (ICP-OES) indicated that AuNP that are 15 nm or smaller have long blood circulation times, while larger AuNP accumulated in the liver and spleen more rapidly. Therefore, while we observed no AuNP size effect on CT contrast generation, there is a significant effect of size on AuNP diagnostic utility.
Funder
National Science Foundation
American Heart Association, United States
Horizon 2020
National Institutes of Health
Publisher
Springer Science and Business Media LLC
Reference71 articles.
1. Hisieh, J. Computed Tomography: Principles, Design, Artifacts, and Recent Advances. SPIE Press PM259, 666 (2015).
2. Chithrani, B. D., Ghazani, A. A. & Chan, W. C. W. Determining the size and shape dependence of gold nanoparticle uptake into mammalian cells. Nano Letters 6(4), 662–668 (2006).
3. Kircher, M. F. & Willmann, J. K. Molecular body imaging: MR imaging, CT, and US. part I. principles. Radiology 263(3), 633–43 (2012).
4. Pelc, N. J. Recent and future directions in CT imaging. Ann. Biomed. Eng. 42(2), 260–268 (2014).
5. Reuveni, T., Motiei, M., Romman, Z., Popovtzer, A. & Popovtzer, R. Targeted gold nanoparticles enable molecular CT imaging of cancer: an in vivo study. Int J Nanomedicine 6, 2859–2864 (2011).
Cited by
175 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献