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Inveon acquisition workplace 1

Manufactured by Siemens
Sourced in United States

The Inveon Acquisition Workplace 1.5.0.28 is a software application that enables the acquisition and analysis of data from various imaging modalities used in preclinical research. It provides a user interface and tools for managing, visualizing, and processing acquired data.

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2 protocols using inveon acquisition workplace 1

1

FDG-PET Imaging in Mice

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Animals were fasted for 6 h prior to the FDG injection and doxycycline treatment was interrupted due to the necessary sucrose addition to the drinking water. ~ 13 MBq FDG in a max. volume of 100 μl were injected i.v. into the tail vein under 1.5% isoflurane narcosis evaporated in oxygen at a flow rate of 0.5 l/min (Abbott, Wiesbaden, Germany) and the animals were kept under anesthesia for 55 min. post-injection in a heated box. Blood glucose and body weight measurements were performed immediately before FDG injection. Subsequently animals were placed on a carbon bed and scanned for 10 min in an Inveon small animal PET scanner (Siemens Preclinical Solutions, Knoxville, TN, USA). Body temperature was maintained at 37 °C by a heating pad and a rectal temperature sensor. Image reconstruction was performed using Inveon Acquisition Workplace 1.5.0.28 (Siemens Preclinical Solutions, Knoxville, TN, USA) with an iterative ordered-subset expectation maximization algorithm (OSEM2D) with four iterations. No attenuation and scatter correction was applied, according to our standard protocol for PET imaging with mice. The reconstructed voxel size was 0.776 × 0.776 × 0.796 mm. Images were analyzed in Inveon Research Workplace (Siemens Preclinical Solutions, Knoxville, TN, USA).
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2

PET Imaging and Quantification of mAb Uptake

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PET images were reconstructed as previously described 11 (link) in Inveon Acquisition Workplace 1.5.0.28 (Siemens Healthineers). Briefly, static histogram files were constructed from list-mode data and images were reconstructed by applying an ordered subset expectation maximization algorithm in two dimensions (Fourier rebinning, OSEM2D, 16 subsets, 4 iterations, pixel size 128x128, matrix 0.79x0.79 mm²). Attenuation correction was not performed. PET images were corrected for radioactive decay, normalized to the amount of injected activity and fused with the anatomical MR images with the help of glass capillaries containing [64Cu]NOTA-αCD11b-mAb solution in Inveon Research Workplace (Siemens Healthineers). Volumes of interest (VOI) were drawn on the lung, liver and spleen on the anatomical MR image, cell uptake in primary tumors and metastases was quantified by drawing VOIs on hot spots on the PET images co-registered to the MR images for anatomical guidance. The percentage of injected dose per cubic centimeter (%ID/cm³) values were calculated as follows: mean activity in VOI/(injected activity*106)/100.
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