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Inveon acquisition workplace

Manufactured by Siemens
Sourced in United States, Germany

The Inveon Acquisition Workplace is a laboratory equipment product designed for imaging and data acquisition. It provides a controlled environment for conducting experiments and collecting data. The core function of the Inveon Acquisition Workplace is to facilitate the capture and analysis of images and other data related to research and experimental processes.

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37 protocols using inveon acquisition workplace

1

Quantifying Abdominal Adipose Tissue Volumes

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Abdominal adipose tissue volumes of visceral and subcutaneous depots were measured with a micro-CT scanner (Siemens Inveon micro-CT, Siemens Healthcare GmbH, Erlangen, Germany; energy settings: 200 mA, 80 kV, 1200 ms) with Siemens Inveon Acquisition workplace software (version 1.2.2.2) before (baseline) drug treatment and after 28 days of chronic infusion of liraglutide or vehicle. Data were reconstructed using filtered back projection and algorithm of Feldkamp in Siemens Inveon Acquisition workplace. The reconstructed data sets were exported to DICOM format using Siemens Inveon Research Workplace and post processed regarding adipose tissue volumes using Materialise MIMICS v.19 (Materialise, Leuven, Belgium). We focused on the abdominal region, as scanning the abdominal adipose depots provides sufficient information to estimate the total body fat and monitor site-specific changes in adiposity and reduces scanning time.13
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2

Small-Animal PET-MRI Imaging Protocol

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For PET/MRI, mice were anesthetized (2% isoflurane at a rate of 2 L of oxygen per minute) and scanned for 10 min on a small-animal PET scanner (Inveon; Siemens Preclinical Solutions) at 2 and 24 h. Subsequently, the mice were transferred to a 7-T BioSpec MRI scanner (Bruker BioSpin MRI). MRI was performed using a whole-body coil and a T2-weighted 3D turbo-RARE (rapid imaging with refocused echoes) sequence (repetition time, 1,800 ms; echo time, 66.7 ms; resolution, 0.3 mm; averages, 2). PET data were reconstructed with a 2-dimensional (2D) ordered-subsets expectation maximization algorithm (matrix, 128 • 128; voxel size, 0.79 • 0.79 mm) in an Inveon Acquisition Workplace (version 1.5.0.28; Siemens). PET and MRI scans were coregistered, and all PET scans were normalized according to the residual activity at the beginning of the respective scan. Different regions (tumor, liver, kidney, and leg muscle tissue) were segmented. humanely killed, and tissues (liver, kidneys, muscle, and tumor) were harvested.
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3

Quantitative Tumor Uptake Analysis

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Mice-bearing xenografts were subjected to 18F-FDG micro-PET/CT analysis performed on an Inveon MM Platform (Siemens, Munich, Germany). Mice were anesthetized with 2% isoflurane before 18F-FDG injection (a single injection of 3.7–7.4 MBq/0.1 mL 18F-FDG via tail vein). 40 min after administration of the tracer, mice were placed on the PET scanner bed and were maintained under continuous anesthesia during the study. Inveon Acquisition Workplace (Siemens) was used for scanning. 3D regions of interest were drawn over the entire tumor guided by CT images, and tracer uptake was measured using Inveon Research Workplace software. The SUV was calculated as decay-corrected activity (kBq) per milliliter of tissue volume/injected 18F-FDG activity (kBq) per gram of body weight.
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4

Fracture Healing and Bone Strengthening in Goats

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Three groups of goats underwent high-resolution scanning of all tibia samples, which were taken from each groups at 4, 8, 12, and 16 weeks after surgery using a micro-CT scanner from Siemens Medical Solutions (USA, Siemens Inc). The radiographic data were collected and reconstructed with the Inveon Acquisition Workplace (USA, Siemens Inc.), and the Inveon Research Workplace (USA, Siemens Inc.) was used to analyse the data. The scanning protocol used was 80 kV and 500 μA, and the effective pixel size was 28.21 μm. Three-dimensional reconstruction of the volume of interest (VOI) in these regions was carried out, and the radiographic images and CT grey values were analysed to evaluate fracture healing and bone strengthening. General analysis was used to obtain coronal-plane, sagittal-plane and horizontal-plane images. Multimodal 3D visualization was used to obtain a stereoscopic image of the fracture and bone plate region.
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5

In Vivo Mouse PET/CT Imaging

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Mouse PET/CT imaging was performed using a Siemens Inveon PET/CT Multi Modality system (Siemens Medical Solutions, Knoxville, TN) with effective spatial resolution of 1.4 mm at the center of field of view (FOV). All animals were fasted for 12 h prior to PET imaging. Each mouse received 140 μCi of 2-deoxy-2-(18F)fluoro-D-glucose (FDG) in 150 μL in saline intravenously via tail vain injection. The mice were placed on a heat pad before and during image acquisition. PET images were acquired 1h post-injection (p.i.), for 15 min, with animals under 2.5% isoflurane. PET images were reconstructed into a single frame using the 3D Ordered Subsets Expectation Maximization (OSEM3D/MAP) algorithm. CT images were acquired immediately after PET with the FOV centered at the shoulder of the mouse. CT projections (360 steps/rotation) were acquired with a power of 80 kVp, current of 500 μA, exposure time of 145 ms, binning of 4, and effective pixel size of 102 μm. The CT reconstruction protocol used a downsample factor of 2, was set to interpolate bilinearly, and used a Shepp-Logan filter. PET and CT images were co-registered in Inveon Acquisition Workplace (Siemens Medical Solutions) for analysis. Regions of interest (ROI) were drawn manually, encompassing the thyroid in all planes containing the organ. The target activity was calculated as percentage injected dose per gram.
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6

Targeted NIS-Mediated Tumor Imaging

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At 3.5–4 weeks after i.c. tumor cell inoculation, polyplexes (monoDBCO-PEG24-GE11/NIS and bisDBCO-PEG24-GE11/NIS polyplexes for EGFR targeting, non-targeted monoDBCO-PEG24/NIS and bisDBCO-PEG24/NIS polyplexes, monoDBCO-PEG24-GE11/LUC and bisDBCO-PEG24-GE11/LUC containing pCMVLuc as additional negative control) with a DNA dose of 2.5 mg/kg (for a 20-g mouse, 50 μg DNA in a total volume of 250 μL; solvent, HBG) were applied systemically via the tail vein. After 24 or 48 h, mice received 10 MBq of 124I (PerkinElmer, Waltham, MA, or DSD Pharma, Purkersdorf, Austria) as an NIS PET tracer by i.v. injection, and NIS-mediated iodide accumulation in tumor areas was determined by small-animal PET (Inveon, SIEMENS Preclinical Solutions, Erlangen, Germany). Serial scanning took place 1, 3, and 5 h after 124I application. Results were assessed with the software Inveon Acquisition Workplace (Siemens, Munich, Germany), were analyzed using Inveon Research Workplace (Siemens), and are represented as a percentage of the injected dose per milliliter tumor (% ID/mL). Mice were pretreated with L-thyroxine (LT4; 5 mg/mL, Sigma Aldrich) in their drinking water 10 days before imaging to reduce thyroidal iodide uptake, and at the same time the mouse chow was changed to a low-iodine diet (ssniff Spezialdiäten GmbH, Soest, Germany).
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7

NIS-Targeted Tumor Imaging in Mice

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Experiments started 2-3 weeks after intrasplenic injection of tumor cells. To demonstrate tumor-specific NIS expression in vivo, mice received polyplexes systemically via the tail vein (i.v.) at a DNA dose of 2.5 mg/kg (50 μg DNA in 250 μL HBG). Mice were treated as follows: (1) LPEI-PEG-GE11/NIS (n=5); (2) LPEI-PEG-Cys/NIS (n=3); (3) LPEI-PEG-GE11/NIS + NaClO4 (n=2): pretreatment with an i.p. injection of 2 mg of the competitive NIS inhibitor sodium perchlorate (NaClO4) 30 min before PET tracer administration. 48 h after polyplex injection the novel NIS PET tracer 18F-TFB (10 MBq; synthesized by the Radiopharmacy, Klinikum rechts der Isar, TU Munich, as described previously [40 (link)]) was applied i.v. and tracer accumulation in metastatic liver areas was determined by small-animal PET (Inveon, SIEMENS Preclinical Solutions, Erlangen, Germany). Regions of interest were analyzed with the software Inveon Acquisition Workplace (Siemens) and quantified using Inveon Research Workplace (Siemens) and expressed as a fraction of the total amount of initial dose (% of ID). The retention time of the tracer 18F-TFB within metastases was determined by serial scanning after 0.5 h, 1 h and 2 h. To suppress thyroidal iodide uptake, a 10-day pretreatment with L-thyroxin (L-T4; 5 mg/ml; Sigma-Aldrich) in drinking water was conducted before PET-imaging.
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8

In Vivo Corrosion Resistance of Implant

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Degradation experiments were carried out using with better. The presented material was implanted in adult Japanese white rabbits (provided by Tianjin Institute of Medical Sciences) to examine its corrosion resistance in vivo. The extrusion rods with a diameter of 8 mm were machined into cylindrical implants with a diameter of 2 mm and a length of 6 mm, which were sterilized by Co60 radiation before surgery. During the operation, the rabbit was anesthetized and the fur on the hind limbs was removed. A hole defect was made in the left femoral condyle with a diameter of about 2 mm. The implant was inserted into the hole and the sutured the myofascial membrane and skin after operation. The operation process was shown in Figure 2. The rabbits were euthanized at 6- and 13-weeks post operation. The Femoral tissues (including implant) were then fixed in 4% paraformaldehyde solution.
The micro-CT scanning was then carried out by Inveon MM CT (SIEMENS, Munich, Germany). The Inveon Acquisition Workplace (SIEMENS, Munich, Germany) and Inveon Research Workplace (SIEMENS, Munich, Germany) software were then used for scanning and data analysis. The COBRA_Exxim (EXXIM Computing Corp., Livermore, CA) software was used for 3D reconstruction and bone parameter analysis.
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9

Micro-CT Analysis of Subchondral Bone

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The left knee joints were then scanned using micro-CT (Inveon, Siemens Medical Solutions, IL, USA) with the following sets: 13-μm isotropic voxel, 80-kV voltage, 500-μA current, 300-ms settling time, 360 projections per 360° and 200-ms exposure time. The obtained raw data were reconstructed using Inveon Acquisition Workplace (Version 5.0, Siemens Medical Solutions USA, Inc., IL, USA). For subchondral trabecular bone analysis, covering the whole subchondral bone in tibial plateaus was selected as the ROI. Bone volume/tissue volume (BV/TV), trabecular number (Tb. N), trabecular thickness (Tb. Th) and trabecular separation (Tb. Sp) were calculated using Inveon Research Workplace (Version 5.0, Siemens Medical Solutions, IL, USA).
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10

NIS-Mediated PET Imaging of Tumor Targeting

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Experiments started 5-6 weeks after intrahepatic injection of tumor cells. For determination of tumor specific NIS expression and subsequent NIS-mediated iodide uptake, animals received LPEI-PEG-GE11/NIS polyplexes for EGFR-targeting (n = 6), LPEI-PEG-cMBP/NIS for cMETtargeting (n = 4) or both for dual-targeting (n = 7). Polyplexes were administered systemically via the tail vein (intravenously, i.v.) at a DNA dose of 2.5 mg/kg (50 μg DNA in 250 μL HBG). At 48 h after polyplex injection mice received the NIS-specific PET tracer 124 I and accumulation in tumor tissue was determined by small-animal PET (Inveon, SIEMENS Preclinical Solutions, Erlangen, Germany). Serial scanning was performed after 1, 3, and 5 h. Regions of interest were analyzed with the software Inveon Acquisition Workplace (Siemens), quantified using Inveon Research Workplace (Siemens) and expressed as a fraction of the total amount of initial dose (% of ID). To suppress thyroidal iodide uptake, a 10-day pretreatment with L-thyroxine (L-T4; 5 mg/ml; Sigma-Aldrich) in drinking water was conducted before PET-imaging. To verify NIS-specific uptake, pretreatment with an intraperitoneal (i.p.) injection of 2 mg of the competitive NIS inhibitor sodium perchlorate (NaClO 4 ) 30 min before PET tracer administration (n = 2) was performed.
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