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Inveon dedicated pet

Manufactured by Siemens
Sourced in Germany

The Inveon™ Dedicated PET is a high-performance preclinical positron emission tomography (PET) imaging system designed for small animal research. It is capable of acquiring high-quality PET data for a wide range of applications, including drug discovery, development, and validation.

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4 protocols using inveon dedicated pet

1

Multimodal Imaging and Therapy Evaluation

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A [18F]-fluorodeoxy-glucose (FDG) reference image was used to evaluate the agent as a diagnostic and therapy follow-up tracer, for each mouse. The mouse was then injected with the imaging and photodynamic therapy bifunctional agent, 124I-labeled pyropheophorbide-a derivative. The long half-life of 124I (4.2d) allowed for multiple scans of the same mouse and the same agent over time (i.e., a longitudinal study). Tumour uptake relative to the rest of the body increased over time. This result indicated that the agent has therapeutic and tumour-monitoring potential. After FDG incubation, a microPET scanner (Inveon™ Dedicated PET, Siemens) was used to obtain an image of each cervix tumour. Iterative reconstruction and segmented attenuation were used to reconstruct the acquisition data. Standard software (Inveon™ Acquisition workplace) was used for the PET image analyses. Fusion and co-registration of the PET and CT data were performed using a software module. However, the data were manually corrected, if necessary. Volumes of interest were placed around the calcified areas for analysis of fused images.
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2

PET Imaging of Tumor Tracers in Mice

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PET imaging was performed simultaneously in four mice using a Siemens Inveon Dedicated PET (Siemens, Erlangen, Germany) for the [18F]FLT scans and a Mediso nanoScan PET/CT (Mediso, Münster, Germany) for the [18F]ML-10 scans. A fifteen-minute transmission scan with an external 57Co point source (Siemens Inveon Dedicated PET) or a low-dose CT (Mediso nanoScan PET/CT) served for attenuation correction. The PET data were acquired in 3-dimensional list-mode after 14.5 ± 1.1 MBq of the tracer had been injected into a tail vein. The [18F]FLT PET was performed 60 to 90 min p.i., the [18F]ML-10 PET was performed 120 to 150 min p.i. The acquired data were reconstructed with attenuation and scatter correction using the software (Inveon Acquisition Workplace 1.528 Service Pack 1, Nucline NanoScan 3.04.018.0000) and reconstruction algorithms provided by the vendors: ordered subset expectation maximisation algorithm with 4 iterations and 26 subsets (32 MAP iter, pixel size (x, y, z): 0.8, 0.8, 0.8 [mm], matrix size (x, y, z): 128, 128, 159 [mm]) on the Siemens Inveon Dedicated PET and 4 iterations and 6 subsets (pixel size (x, y, z): 0.4, 0.4, 0.4 [mm], matrix size (x, y, z): 212, 212, 239 [mm]) on the Mediso nanoScan PET/CT. Reconstruction parameters for the two devices were chosen for equivalent spatial resolution.
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3

Small Animal PET Imaging Protocol

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Small animal PET images were acquired using the Inveon dedicated PET (Siemens Preclinical Solutions, Erlangen, Germany). Approximately 7.4MBq (200 μCi) of [18F]FHBG (Stanford Radiochemistry Facility, Stanford, CA) was intravenously injected per mouse, and 10-min static PET scans were obtained 30 min later. Additionally, 10-minute transmission scans for PET attenuation correction were also acquired. Following PET acquisition, mice were immediately transferred to the GNEXT PET/CT (SOFIE, Culver City, CA) to acquire corresponding CT images for anatomical co-registration. Images were co-registered and region of interest (ROI) analysis was performed with a 3D volume drawing mode using the Inveon Research Workplace Software (Siemens Preclinical Solutions).
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4

Multimodal Imaging for Tumor Monitoring

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A Bruker Biospec 94/24 USR (9.4T) small animal scanner (35-mm diameter birdcage coil, Bruker BioSpin MRI, Ettlingen, Germany) was used to obtain MR images. T2-weighted images were obtained using rapid acquisition setting. They were acquired at the beginning inside the magnet bore. A 1.5% isoflurane and O2/N2O (1:1) mixture at flow rate of 0.7 L/min was used for anesthesia during MR experiment.
[18F]-fluorodeoxy-glucose (FDG) image was acquired as a reference to evaluate the agent as a diagnostic and therapy follow-up tracer. The same mouse was then injected with a 124I-la-beled derivative of pyropheophorbide-a, an imaging and photodynamic therapy bifunctional agent. Because of the long half-life of 124I (4.2 days), a longitudinal study (multiple scans over time) was possible with the same mouse and the same agent. Tumor uptake relative to the rest of the body increased over time, indicating that the agent had promising potential as both a therapeutic and a tumor-monitoring agent. After incubation with FDG, endometrial tumors were imaged using a microPET scanner (Inveon™ Dedicated PET, Siemens). PET image analyses were then performed using a standard software (Inveon™ Acquistion workplace).
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