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Inveon acquisition workplace iaw

Manufactured by Siemens
Sourced in Germany

The Inveon Acquisition Workplace (IAW) is a laboratory equipment product offered by Siemens. It is designed to serve as a workstation for data acquisition and analysis. The IAW provides an integrated platform for managing experimental data and performing necessary operations.

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5 protocols using inveon acquisition workplace iaw

1

Rabbit Micro-Angiography for Vascular Assessment

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Six rabbits underwent micro-angiography at 2 and 4 weeks after operation. Under general and deep anesthesia, the thoracic cavity was opened. The aorta was cannulated with an 18-gauge venula needle and flushed with heparinized saline, then, the vena cava was severed for an outlet. After limpidity of the fluid from vena cava, contrast agent (Microfil MV-122 [yellow]; Flow Tech, USA) was injected in the aorta according to the manufacturer’s protocol (Fig. 5B) [33 (link)]. The animals were then euthanasia and stored at 4°C overnight. In the second day, the implants were harvested, fixed with 4% paraformaldehyde solution for 3 days. Micro-CT scanner (μCT; Inveon, Siemens, Germany) was used for the assessment of blood vessels volume in specimens. The colorful images of the implants were reconstructed with standardized thresholds for further quantitative analysis of the blood vessel volume/total volume (BV/TV) ratio by Inveon Acquisition Workplace (IAW, Siemens, Germany).
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2

Quantifying Bone Ingrowth in Spinal Implants

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After X-ray examination, each specimen underwent micro-CT scanning using Siemens micro-CT system (Inveon CT scanner, Siemens, Germany) at 80 kV, 500 μA, and a spatial resolution of 30 μm. The acquired data (DICOM format) were exported and processed using Inveon Acquisition Workplace (IAW) (Siemens, Germany). A cylinder (diameter: 6.0 mm, length: 10 mm) with a hemispherical (diameter: 6.0 mm) tip was defined as the region of interest (ROI), covering the decompressive channel in the CD group or the porous titanium rod in the rod insertion group. New bone ingrowth in the ROI of each specimen was reconstructed with the threshold of 200-1400 for bone and 1400-4095 for implant, and the ratio of new bone volume to total volume (BV/TV) and the mean bone trabecular thickness in each ROI were calculated.
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3

Quantitative Microstructural Analysis of Bone Defects

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Quantitative analysis of the microstructure of animal samples was performed by microelectronic computed tomography (μCT; Inveon, Siemens, Germany). First, the specimens were scanned along the longitudinal axis with a slice thickness of 15 μm at 90 kV and 56 mA current. The data obtained after scanning were passed through Inveon Acquisition Workplace (IAW, Siemens, Germany) software to reconstruct 3D images of the region of interest (ROI, Ø 6.0 × 6.0 mm) containing the repair area. The osteogenic indices BV/TV (ratio of bone volume to the total defect volume), RV/TV (ratio of residual material volume to the total defect volume), and Tb⋅N (number of bone trabeculae) were quantified for the bone defects of the ROI.
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4

Femoral Defect Repair Analysis

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After harvesting, the femoral specimens were scanned using a special imaging system (XPERT; Kubtec Co., Stratford, CT) designed for small animals. To provide a preliminary assessment of scaffolds degradation and new bone formation, the lateral X-ray films of each group (n =4) were recorded at 45 kV and 100 μA. All of the films were recorded using a high-resolution camera (DMLA; Leica, Wetzlar, Germany). Repair effect of femoral defect was evaluated by micro-computed tomography (micro-CT; Inveon™ CT scanner, Siemens, Berlin, Germany) and all specimens were scanned vertically along the long bone axis covering the entire distal femur with a current of 80 mA and a voltage of 80 kV. That’s how the region of interest (ROI; 6.5 × 5.0 × 5.0 mm) was traced manually and virtually 3D reconstructed. For quantitative analysis, the newly formed bone (NB) volume-to-total volume (BV/TV), material residual/total volume (RV/TV) and trabecular number (Tb.N) were calculated using Inveon Acquisition Workplace (IAW; Siemens, Berlin, Germany).
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5

Small-Animal PET Imaging of PSMA Ligands

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For small-animal PET imaging, the different 68Ga-labeled PSMA ligands (0.5 nmol, 20 MBq in approximately 100 µL 0.9% saline) were injected into C4-2 tumor bearing mice. The dynamic PET was recorded in a small animal PET scanner (Siemens Inveon D-PET). The standardized uptake values (SUVs) were obtained from conventional (non-dynamic) PET images. The formula for the SUV was SUV=activityinROI (Bqml) × animalweight (g)injecteddose(Bq)
Manual delineation of the respective appropriate whole organ (heart, kidneys, bladder, tumor, with an approximate volume of 100–500 µL) yielded the volumes of interest (VOIs). For this purpose, whole organs or parts of the organ/tissue (liver and muscle) were used. The images were reconstructed based on the procedure: OSEM 3D/SP MAP with 16 subsets, two iterations, and an image x-y size: 256, image z size: 161. The data were not modified with a post-processing filter. Analysis of the images and time-activity curves (TACs) was conducted on the Inveon™ Acquisition Workplace (IAW) from Siemens IRW 4.1. Dynamic PET scans were performed 0–60 min p.i., and images were reconstructed in three time frames of 20 min (0–20 min, 20–40 min, and 40–60 min) for visual display. A static PET scan was generated at 1 h post injection. The mean SUVs were plotted over time in order to compare the different radiotracers.
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