SU-D-217A-01: A High-Resolution in Vivo Molecular Imaging Technique Based on X- Ray Fluorescence

2012 ◽  
Vol 39 (6Part3) ◽  
pp. 3620-3620
Author(s):  
P Chtcheprov ◽  
Y Lee ◽  
J Lu ◽  
O Zhou
2021 ◽  
Vol 23 (Supplement_6) ◽  
pp. vi230-vi230
Author(s):  
Sadaf Soloukey ◽  
Luuk Verhoef ◽  
Frits Mastik ◽  
Bastian Generowicz ◽  
Eelke Bos ◽  
...  

Abstract BACKGROUND Neurosurgical practice still relies heavily on pre-operatively acquired images to guide tumor resections, a practice which comes with inherent pitfalls such as registration inaccuracy due to brain shift, and lack of real-time functional or morphological feedback. Here we describe functional Ultrasound (fUS) as a new high-resolution, depth-resolved, MRI/CT-registered imaging technique able to detect functional regions and vascular morphology during awake and anesthesized tumor resections. MATERIALS AND METHODS fUS relies on high-frame-rate (HFR) ultrasound, making the technique sensitive to very small motions caused by vascular dynamics (µDoppler) and allowing measurements of changes in cerebral blood volume (CBV) with micrometer-millisecond precision. This opens up the possibility to 1) detect functional response, as CBV-changes reflect changes in metabolism of activated neurons through neurovascular coupling, and 2) visualize in-vivo vascular morphology of pathological and healthy tissue with high resolution at unprecedented depths. During a range of anesthetized and awake neurosurgical procedures we acquired vascular and functional images of brain and spinal cord using conventional ultrasound probes connected to a research acquisition system. Building on Brainlab’s Intra-Operative Navigation modules, we co-registered our intra-operative Power Doppler Images (PDIs) to patient-registered MRI/CT-data in real-time. RESULTS During meningioma and glioma resections, our co-registered PDIs revealed fUS’ ability to visualize the tumor’s feeding vessels and vascular borders in real-time, with a level of detail unprecedented by conventional MRI-sequences. During awake resections, fUS was able to detect distinct, ESM-confirmed functional areas as activated during conventional motor and language tasks. In all cases, images were acquired with micrometer-millisecond (300 µm, 1.5–2.0 ms) precision at imaging depths exceeding 5 cm. CONCLUSION fUS is a new real-time, high-resolution and depth-resolved imaging technique, combining favorable imaging specifications with characteristics such as mobility and ease of use which are uniquely beneficial for a potential image-guided neurosurgical tool.


Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Dong Oh Kang ◽  
Yong Geun Lim ◽  
Joon Woo Song ◽  
Ye Hee Park ◽  
Hyun Jung Kim ◽  
...  

Background/Objectives: Vascular spotty calcification is an actively regulated biological process resulting in plaque vulnerability. We investigated the feasibility of a novel alendronate-based near-infrared fluorescence (NIRF)-emitting probe to specifically target atherosclerotic calcification in a murine model in vivo using our customized high-resolution multichannel intravital molecular imaging system (IVFM). Methods/Results: We have fabricated a calcium-binding NIRF probe by chemically coupling alendronate, a specific targeting ligand, and NIRF-emitting Cy5.5 to the ends of azide-PEG-NHS ester (Al-Cy5.5). Prepared Al-Cy5.5 has high affinity for calcium phosphate-containing bone minerals. In vitro, Al-Cy5.5 specifically binds to RANKL-induced osteogenic-macrophages as compared to macrophages (p<0.01). On whole body fluorescence imaging to assess time-dependent excretion, NIRF signals remained visible up to 48 hrs. Then, in mice with calcified plaque induced by a combination diet of high-cholesterol and warfarin, Al-Cy5.5 (2.5 mg/kg) was intravenously injected. 48 hrs after administration, murine calcified atheroma was assessed using a customized high-resolution multichannel IVFM, which demonstrated highly enhanced NIRF signals in vivo in the calcified areas of murine carotid plaques (p<0.01, Figure). Ex vivo laser scanning fluorescence microscopic and immune-histological findings from the corresponding sister sections well corroborated the in vivo imaging results, which demonstrated the co-localization of NIRF signals with plaque calcifications (von-Kossa stain). Conclusions: Our novel calcification targeted probe, Al-Cy5.5, was able to selectively target atheroma calcification in vivo in a murine model as assessed by optical IVFM. This novel targetable strategy is expected to provide a promising theranostic basis for calcified high-risk plaques by integration with multimodal customized catheter imaging system.


2008 ◽  
Vol 33 (21) ◽  
pp. 2494 ◽  
Author(s):  
Qingkai Huo ◽  
Tetsuya Yuasa ◽  
Takao Akatsuka ◽  
Tohoru Takeda ◽  
Jin Wu ◽  
...  

2007 ◽  
Vol 17 (01n02) ◽  
pp. 41-46 ◽  
Author(s):  
Y. KAWAMURA ◽  
K. ISHII ◽  
H. YAMAZAKI ◽  
S. MATSUYAMA ◽  
Y. KIKUCHI ◽  
...  

We have developed “micron-CT”, using micro-PIXE for in-vivo imaging. This system comprises an X-ray CCD camera (Hamamatsu photonics C8800X9) with high resolution (pixel size: 8×8 μm 2, number of pixels: 1000×1000) and an X-ray-point-source with a spot size of 1.5×1.5 μm 2 which is generated by irradiation of a microbeam on a pure metal target. Thus we can acquire projection data with high resolution. The sample is placed in a small diameter tube and is rotated by a stepping motor. The 3D images were reconstructed from the obtained projection data by using cone-beam CT reconstruction algorithm. X-ray spectra produced by heavy charged particle bombardment, exhibit a much smaller continuous background compared to electron bombardment. Therefore, X-rays produced by ion beam can be used as a monochromatic and low energy X-ray source. The feature is very effective to investigate small insects. Moreover we can get elemental distribution image of object by choosing appropriate characteristic X-rays corresponding to the absorption edge. On the other hand, the conventional X-ray CT, in which continuous X-rays are used, provides images of the electron density in the object. Using this system, we were able to get 3D images of a living ant's head with 6 μm spatial resolution. By using Fe - K -X-rays (6.40 keV) and Co - K -X-rays (6.93 keV), we can investigate the 3D distribution of Mn ( K -absorption edge = 6.54 keV) in an ant's head.


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