Metallic nanoparticles as X-Ray computed tomography (CT) contrast agents: A review

2020 ◽  
Vol 1219 ◽  
pp. 128599 ◽  
Author(s):  
Naim Aslan ◽  
Burhan Ceylan ◽  
Mümin Mehmet Koç ◽  
Fehim Findik
2010 ◽  
Vol 21 (24) ◽  
pp. 245104 ◽  
Author(s):  
Chie Kojima ◽  
Yasuhito Umeda ◽  
Mikako Ogawa ◽  
Atsushi Harada ◽  
Yasuhiro Magata ◽  
...  

2007 ◽  
Vol 2 (6) ◽  
pp. 292-293
Author(s):  
S. Roux ◽  
C. Alric ◽  
J. Taleb ◽  
C. Mandon ◽  
C. Billotey ◽  
...  

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Jun Xie ◽  
Zonglang Zhou ◽  
Sihan Ma ◽  
Xian Luo ◽  
Jiajing Liu ◽  
...  

AbstractX-ray computed tomography (CT) has been widely used in clinical practice, and contrast agents such as Iohexol are often used to enhance the contrast of CT imaging between normal and diseased tissue. However, such contrast agents can have some toxicity. Thus, new CT contrast agents are urgently needed. Owing to the high atomic number (Z = 83), low cost, good biological safety, and great X-ray attenuation property (5.74 cm2 kg−1 at 100 keV), bismuth has gained great interest from researchers in the field of nano-sized CT contrast agents. Here, we synthesized BiF3: Ln@PVP nanoparticles (NPs) with an average particle size of about 380 nm. After coating them with polyvinylpyrrolidone (PVP), the BiF3: Ln@PVP NPs possessed good stability and great biocompatibility. Meanwhile, compared with the clinical contrast agent Iohexol, BiF3: Ln@PVP NPs showed superior in vitro CT imaging contrast. Subsequently, after in situ injection with BiF3: Ln@PVP NPs, the CT value of the tumor site after the injection was significantly higher than that before the injection (the CT value of the pre-injection and post-injection was 48.9 HU and 194.58 HU, respectively). The morphology of the gastrointestinal (GI) tract can be clearly observed over time after oral administration of BiF3: Ln@PVP NPs. Finally, the BiF3: Ln@PVP NPs were completely discharged from the GI tract of mice within 48 h of oral administration with no obvious damage to the GI tract. In summary, our easily synthesized BiF3: Ln@PVP NPs can be used as a potential clinical contrast agent and may have broad application prospects in CT imaging.


2014 ◽  
Vol 26 (1) ◽  
pp. 111-118 ◽  
Author(s):  
Detlev Sülzle ◽  
Marcus Bauser ◽  
Thomas Frenzel ◽  
Gregor Jost ◽  
Hubertus Pietsch ◽  
...  

2012 ◽  
Vol 1 (4) ◽  
pp. 413-431 ◽  
Author(s):  
Anshuman Jakhmola ◽  
Nicolas Anton ◽  
Thierry F. Vandamme

2010 ◽  
Vol 12 (5) ◽  
pp. 463-467 ◽  
Author(s):  
Bulent Aydogan ◽  
Ji Li ◽  
Tijana Rajh ◽  
Ahmed Chaudhary ◽  
Steven J. Chmura ◽  
...  

2017 ◽  
Vol 56 (10) ◽  
pp. 5757-5761 ◽  
Author(s):  
Markus Berger ◽  
Marcus Bauser ◽  
Thomas Frenzel ◽  
Christoph Stephan Hilger ◽  
Gregor Jost ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Yuxi C. Dong ◽  
Maryam Hajfathalian ◽  
Portia S. N. Maidment ◽  
Jessica C. Hsu ◽  
Pratap C. Naha ◽  
...  

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.


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