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Vivoquant imaging software

Manufactured by Invicro
Sourced in United States

VivoQuant Imaging Software is a comprehensive image analysis platform designed for preclinical imaging data. It provides tools for visualization, processing, and analysis of multimodal imaging data, including PET, SPECT, CT, and MRI.

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5 protocols using vivoquant imaging software

1

Quantitative MPI Imaging of Islet Organoids

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In vitro phantoms comprising of different numbers of VivoTrax labeled islet organoids (0, 25, 50, 100, 200, and 400) in PBS were imaged using an MPI scanner (MOMENTUM MPI, Magnetic Insight Inc., Alameda, CA, United States) with the fiducial markers. Each 2D MPI images were acquired with parameters of a field-of-view (FOV) of 6 cm × 12 cm, a 5.7 T/m selection field gradient, a drive field strength of 20 mT peak amplitude and a 45.0 kHz drive frequency. Images were reconstructed using x-space reconstruction. Quantification of the islet organoids phantoms was performed using the 2D MPI image intensity calibrated against a fiducial marker of known iron content (2.2 μg of iron) using VivoQuant imaging software (Invicro, Boston, MA, United States).
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2

In Vivo Islet Organoid Imaging

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Under anesthesia with 2% isoflurane, mice were imaged using 3D MPI at 1, 7, and 28-day post-transplantation (n = 3) with operating parameters, a FOV of 6 cm × 6 cm × 12 cm, acquisition time of 10 s per projection (total 55 projections) plus 30 s for automatic set up of the magnets, with an approximate total time of 35 min including for image reconstruction. Anatomic CT reference images were acquired by the whole-body model of Perkin Elmer QuantumGX microCT. MPI images were co-registered to CT with fiducial markers using VivoQuant Imaging Software (Invicro, Boston, MA, United States). Control animals did not receive islet organoids (n = 2).
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3

Validating TIV Prediction Algorithm Accuracy

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In order to measure accuracy of the algorithm and determine its validity, its TIV prediction was compared to that of a manual rater, in this case a board-certified radiologist. The rater segmented the ROI manually on 15 images using the VivoQuant Imaging Software (Invicro, Boston, MA, United States), and total pixel sum values were extracted for TIV analysis from the ROIs using a ratio method with reference to a singular fiducial marker for TIV prediction (Makela et al., 2020 (link)), calibrated against a 40% fiducial marker of known iron concentration (2.2 μg of iron). For statistical analysis, SPSS statistical software (IBM, Armonk, NY, United States) was used to calculate intraclass correlation coefficient (ICC), which provides a measure of the inter-rater reliability between the rater and algorithm. A two-way mixed model with a confidence interval of 95% was selected, and a measure of absolute agreement was calculated with the ICC. A higher ICC score indicates greater reliability of algorithm performance due to the high degree of agreement between the rater and algorithm.
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4

Radiolabeling and PET/CT Imaging of PSMA-11

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68Ga-PSMA-11 was synthesized by eluting gallium-68 from a 68Ge/68Ga generator (Eckert & Ziegler) with 0.1 M hydrochloric acid, trapping 68Ga on a cationic exchange cartridge and eluting with 5 M sodium chloride solution. 5 µg PSMA-11 in HEPES buffer were reacted with 68GaCl3 for 5 min at 95 °C. Radiochemical identity and purity were confirmed before application by radiographic thin-layer chromatography. For PET/CT, ~1.1 MBq 68Ga-PSMA-11 in 100 µL volume was injected into the tail vein and images were acquired 60 min later using the pre-clinical Genisys 8 PET/CT scanner (Sofie Biosciences). Attenuation corrected images were reconstructed using maximum-likelihood expectation maximization with 60 iterations. The following parameters were applied for CT imaging: 40 kVp, 190 mA, 720 projections, and 55 ms exposure time per projection. The resulting PET/CT images were analysed using the VivoQuant Imaging Software (Invicro).
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5

Comparative Evaluation of PSMA-Targeted PET Imaging Agents

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NSG mice bearing subcutaneous C4-2 tumors underwent PET/CT imaging with each of the following compounds on consecutive days: 68Ga-PSMA-11, 68Ga-PSMA-617, and 68Ga-PSMA-TO-1 in the same 3 mice. Average tumor volumes over the 3 days were 660 ± 35 mm3, 190 ± 32 mm3 and 243 ± 1.5 mm3 for mouse 1, 2 and 3, respectively. PET images were acquired 60 min after intravenous administration of 1.1 MBq 68Ga-PSMA in 100 µL volume (PSMA-TO-1 on day 1; PSMA-11 on day 2; PSMA-617 on day 3) using the preclinical Genisys 8 PET/CT scanner (Sofie Biosciences). Attenuation-corrected images were reconstructed using maximum likelihood expectation–maximization with 60 iterations. The following parameters were applied for CT imaging: 40 kVp, 190 mA, 720 projections, and 55-ms exposure time per projection. The resulting PET/CT images were analyzed for tumor volume and percent injected activity uptake per gram using VivoQuant Imaging Software (Invicro, Boston, MA). One-way ANOVA with Bonferroni’s multiple comparisons test was used to compare the tumor uptake of each ligand.
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