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Ge explore ct120

Manufactured by GE Healthcare
Sourced in Canada, United Kingdom

The GE eXplore CT120 is a compact and high-performance computed tomography (CT) scanner designed for preclinical research. It offers state-of-the-art imaging capabilities for the study of small animal models.

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4 protocols using ge explore ct120

1

Radiotherapy Delivery System with Iris Collimation

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The GE eXplore CT120 (GE Healthcare, London, Ontario, Canada) was adapted to radiotherapy delivery by adding a two-stage iris collimation system (Rodriguez et al 2009 (link)). This system utilizes a pulsed x-ray beam running a ~10% duty cycle with a 0.3 mm focal spot for imaging, in contrast to using a continuous imaging beam on the PXi and Xstrahl units (Zhou et al 2010 (link)). The amorphous silicon flat panel detector has a pixel size of 49 μm and the SID and SSD are 35.4 cm and a 45 cm, respectively. MicroCT imaging on the GE eXplore CT120 scanner is performed with tube voltages between 70 and 120 kVp and radiotherapy with the maximum tube voltage of 120 kVp and tube current of 60 mA, using 1–10 cm diameter circular collimation with ~2 Gy min−1 maximum output. The GE eXplore CT/RT140 microCT imaging is performed in similar fashion to the imager of the GE eXplore CT120 scanner (Jensen et al 2013 (link)). Radiotherapy is performed at 140 kVp with a 1.0 mm focal spot with a set of computerized independent jaws and the same SID as the eXplore CT120.
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2

Micro-CT Guided Small-Animal Radiotherapy

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We previously developed an integrated micro-computed tomography (CT)/RT system capable of sophisticated image-guided conformal small-animal radiotherapy [22] (link). The microirradiation technology is based on a modified preclinical micro-CT system (GE eXplore CT 120, GE Healthcare, Milwaukee, WI) with an upgraded x-ray generator (140 kVp, 50 kW), custom irradiation control software (Parallax-Innovations, London, ON, Canada), and a custom-built computer-controlled collimator. Thus far, it had been used for respiratory-gated rat lung irradiation and was commissioned for mouse WBRT in this work [22] (link), [23] (link). Mice were anesthetized (1.5% isoflurane in oxygen), placed feet first prone on the rodent couch, and aligned using setup lasers and CT imaging. On-board fluoroscopy was used to identify the skull and position computerized collimators such that the whole brain was targeted for irradiation and the remainder of the head and body was shielded. Animal temperature was maintained using a heating pad, and breathing rate was monitored during treatment.
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3

Temporal Bone Defect Evaluation

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The animals were anesthetized and placed in ventral recumbancy on the GE LightSpeed 16 Slice CT scanner (GE Medical Systems). The scans (0.625 mm resolution, 120 kV) were conducted on all animals at 2 months pre-surgery, immediately, and at 6 weeks, 3 months, and 6 months following surgery. μCT imaging (50 μm resolution, 100 kV) of harvested RCUs was done using the GE Explore CT-120 (GE Medical Systems) at an external facility (Cornell University Imaging Facility), in a blinded fashion. Condyle height and bone volume were measured using the Mimics software (Materialise). Quantitation of bone volume and bone volume fraction was conducted by determining the amount of bone in the defect area based on the difference between the CT of pre- and post- surgery and the amount of bone removed.
μCT was performed by using a modified protocol (47 (link)), and the samples were scanned at 21-μm isotropic resolution. The bone volume was obtained from the application of a global thresholding technique so that only the mineralized tissue was detected. There was no difficulty in distinguishing the grafted material from the miniplates and screws used for fixation, which appeared in μCT as compact and geometrically defined structures. Spatial resolution of the full-voxel model was sufficient for evaluating the microarchitecture of the bone tissue.
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4

Assessment of Stent Morphology and Fracture

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Two approximately perpendicular radiographs were taken to document stent location and morphology in situ. Following necropsy, additional radiographs were obtained to assist in assessment of expanded stent morphology, damage and/or strut fracture sites. Post-embedding of the stented arteries in resin, microCT was performed on each sample (GE eXplore CT 120, 50 micron resolution; Little Chalfont, UK). The microCT scans, in DICOM format, were viewed and segmented for isolation of each stent specimen and then converted to a sold representation (SCANIP v7; Simpleware, UK). Following 3D reconstruction, each specimen was inspected for fracture or discontinuities (Figure 3). Particular attention was paid to the pre-fracture site locations in order to verify successful micro-cutting of the stent struts.
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