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Inveon multimodality system

Manufactured by Siemens
Sourced in Germany

The Inveon Multimodality System is a versatile imaging platform that combines multiple imaging modalities, including Positron Emission Tomography (PET), Computed Tomography (CT), and Single Photon Emission Computed Tomography (SPECT). It is designed for preclinical research applications.

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8 protocols using inveon multimodality system

1

Microstructural Analysis of Freshwater Fish Skulls

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A subset of individuals from the ecomorphological analyses was subjected to microcomputed tomography (microCT) scanning. From north to south: Lake Catemaco (Astyanax n = 2, Bramocharax n = 3); Lake Ocotalito and the Lacanjá river in the Usumacinta basin, Mexico (Astyanax n = 5, Bramocharax n = 9); Lake Managua (Astyanax n = 4, Bramocharax n = 3); and Lake Nicaragua (Astyanax n = 4, Bramocharax n = 6; Table S1). Specimens were shipped to the University of Cincinnati Vontz Core Imaging Laboratory (Cincinnati, OH) for microCT scanning. The Inveon Multimodality System (Siemens, Munich, Germany) was used to collect 2D slices in the axial, coronal, and sagittal orientations. Slices were stored as DICOM formatted files and reconstructed into 3D volume-rendered images (Figure 1) using Amira software. Bone was labeled based on density using the “label field” tool in Amira and segmented to create a 3D surface file of the skull.
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2

Micro-CT Imaging of Tissue Samples

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All tissues were maintained in PBS while being imaged via micro‐CT, as previously described.12 Briefly, imaging was done using a Siemens Inveon Multimodality System (San Diego, CA) in the University of Cincinnati Vontz Imaging Laboratory facility (VCIL), with high magnification, resulting in an effective voxel size of 17.3 microns. Image analysis and figure preparation were done with an Inveon software package or ImageJ (NIH), from DICOM image file stacks, using either 3D reconstructions or single frames. A movie of one stack was made using ImageJ (Supplementary information).
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3

Xenograft PET/CT Imaging in NOD/SCID Mice

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Fasting NOD/SCID mice bearing xenografts were subjected to 18F-FDG micro-PET/CT analysis performed with an Inveon Multimodality system (Siemens, Munich, Germany). Mice were anaesthetised with isoflurane prior to a single injection of 3.7 MBq 18F-FDG via the tail vein. Forty minutes after administration of the tracer, mice were placed on the PET scanner bed and maintained under continuous anaesthesia during the study. The standardised uptake value (SUV) was calculated as follows: decay-corrected activity (kBq) per mL of tissue volume/injected 18F-FDG activity (kBq) per g of body weight53 (link).
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4

Micro-CT Analysis for Locating TC Junctions

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During pouring of the TMM into the fixture, TC wires could be displaced slightly from their original position. As a result, high resolution micro-CT (Inveon Multimodality System, Siemens Inc., Germany) was used to scan the tissue phantoms, in order precisely determine the location of the TC junctions, which are later used in the inverse algorithm [17 (link)]. The processing software used in conjunction with the CT scan images was Inveon Research Workplace 4.2. The acquisition software used for obtaining the CT images was Inveon Acquisition Workplace (IAW) 2.0.2. The micro-CT images obtained with a voxel size of 36 μm were brighter for tissue phantoms with higher mNPs concentration compared to the control phantom. Fig 3 shows the TC junctions as bright spots inside the phantom. The position of these junctions were determined for the control phantom and the phantoms containing 0.0047% and 0.047% mNPs. The TC junction locations were later used in determining the focal location of the beam.
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5

Micro-CT Analysis of Pig Bone Trabeculae

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In this study, Micro-CT (Inveon Multimodality System, Siemens Medical Solutions, Malvern, PA, USA) was used for microstructural analysis of cancellous bone samples collected from the rib area of pigs, which were obtained from local commercial slaughterhouses. Figure 1 shows the extraction process of related parameters of bone trabeculae. The selected bone trabeculae samples were divided into three layers for extraction and then divide each layer into five 2 mm sided cubes. A separate color was assigned to each segmented model for later statistical analysis. A total of 10 bone trabecular models were selected and 150 samples were extracted for reconstruction and parameter measurement. The porosity of each model was counted in the range of 40% to 80% in 5% increments. The results were shown in Figure 1. The results showed that the average porosity of the block mode l was 58.9%, which was concentrated in the range of 55–65%, accounting for 83.4% of the total samples. Therefore, in this study, the porosity of the bionic scaffold was selected as 55–65%, and the porosity of the test model was determined to be 55%, 57%, 59%, 61%, 63%, 65% at the interval of 2%. The average thickness of bone trabeculae in the region was calculated to be 0.209 ± 0.004 mm.
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6

Imaging Mg Filament Degradation via Micro-CT

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To image Mg filament degradation, conduits containing Mg (in saline for imaging) were assessed by micro-CT in a Siemens Inveon Multimodality System (San Diego, CA) at the University of Cincinnati Vontz Imaging Core Facility. Samples were scanned at half-degree increments with 384 steps (step and shoot) for 192°. Images were acquired with high magnification and a pixel matrix binning of 2, resulting in an effective voxel size of 17.27 μm, using 80 kVp voltage and 300 μA current, with the exposure time being 2100 ms with 25 ms settle time. Inveon software was used to create three-dimensional reconstructions and then single frames were selected for figures.
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7

Radiolabeled Peptide Synthesis and Evaluation

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The NOTA was purchased from Macrocyclic, Inc; protected amino acids, other peptide synthesis reagents, and resins were obtained from Nanchang tanzhenbio Co., Ltd; anhydrous aluminum chloride (AlCl3) and sodium acetate were purchased from Alfa Aesar (China) Chemicals Co., Ltd; and trifluoroacetic acid (TFA) was obtained from Shanghai Aladdin Biochemical Technology Co., Ltd. (China). Reagents, including phosphate-buffered saline (PBS) and cell culture medium, were obtained from Sigma-Aldrich. Fetal bovine serum (FBS) was purchased from Biological Industries (BI) company. All reagents and solvents were commercial products and used without further purification. The Siemens Cyclotron produced [18F] fluoride by bombarding a [18O] H2O target with 12.5 MeV protons. Analytical HPLC (high-performance liquid chromatography) was performed on an Agilent 1200 system with a reversed-phase column (Agilent Zorbax ODS, 250 × 4.6 mm). Mass spectra were obtained on a Q-T of a premier UPLC system equipped with an electrospray interface (ESI) (Waters, USA). A γ-counter (CAPRA-R, Capintec, Inc., Ramsey, New Jersey, USA) was used to measure the radiation value of the biological distribution experiment. Small animal imaging was performed using a micro-PET/CT scanner (Siemens Inveon Multimodality System, Germany).
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8

Visualizing MALAT-1 Expression in Tumor Mice

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Mice with MHCC-LM3 tumours were divided into group 1 (antisense group), 2 (sense group) and 3 (blocked group), (n=4 for each group). Mice were injected with 0.1 mL of 68 Ga-MALAT-1 ASO (3.7 MBq) via tail vein. The images were performed at 30, 60 and 90 min after injection using a micro PET/CT scanner (Siemens Inveon MultiModality system) while the mice were maintained under iso urane anaesthesia (1.5% iso urane, 3% oxygen). A blocking study was performed in which 100 nmol of unlabelled MALAT-1 ASO was intravenously administered 30 min before the intravenous injection of 68 Ga-MALAT-1 ASO (3.7MBq). Three-dimensional volumes of interest (VOIs) were used for the assessment of %ID/g and standard uptake value (SUV) in selected organs.
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