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R4 micropet

Manufactured by Siemens
Sourced in United States

The R4 microPET is a small-animal positron emission tomography (PET) imaging system designed for preclinical research. It is capable of high-resolution imaging of small animals such as mice and rats. The R4 microPET provides quantitative information about biological processes at the molecular level.

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5 protocols using r4 micropet

1

In vivo Imaging of Dectin-1 Knockout Mice

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Positron Emission tomography (PET)/computed tomography (CT) imaging was conducted in C57BL/6 and Dectin-1−/− mice 48 h after IP injection of 1 mg of pure 89Zr-WGP or injection of 1 × 106 peritoneal macrophages that had been co-cultured with 25 μg/ml of 89Zr-WGP for 2 h and then gently washed to remove excess 89Zr-WGP. The mice were scanned for 15 min with a Siemens R4 MicroPET followed by 10 min of CT scan. Siemens IAW software was used for the acquisition and reconstruction of the PET signal, and Siemens IRW software was used for merging and analyzing the imaging data. At the end of the imaging study, mice were euthanized, and organs of interest were harvested. For biodistribution, 50 uL of peripheral blood was collected using a retro-bulbar bleeding technique. The brain, heart, lungs, liver, spleen, kidneys, pancreas, large intestine, small intestine, stomach, femur, a piece of skin from the flank of the mice, and the rectus femoris muscle were harvested, weighed, and placed in a 2470 Wizard automatic gamma counter (PerkinElmer) in order to measure the radioactivity of each tissue. The CPM values were calculated using Prism software (GraphPad Software, La Jolla, CA).
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2

Multitracer microPET Imaging of Mice

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An R4 microPET (Siemens Medical Solutions USA, Inc.) was used for imaging, which has an approximate resolution of 2 mm in each axial direction (20 (link)). After a tail vein injection of (3.7±0.3) x 106 Bq of 18F-FP-PRGD2, 18F-FLT, 18F-FDG or 18F-FAZA in 100 μL of PBS, a 3-min prone acquisition scan was performed approximately 60 min after injection (90 minutes for 18F-FAZA). A heating pad, heat lamp, or hot water was used to dilate the tail veins for injections.
Except for those injected with 18F-FDG, the mice were maintained under isoflurane anesthesia during the injection and scanning periods only. In between, the mice were given ad libitum access to food and water. For mice injected with 18F-FDG, the mice were fasted 6-hours before the injections and were kept under anesthesia between the injection and scanning sessions. For all experiments, the mice were kept warm using a heating pad or heat lamp while under anesthesia to maintain a body temperature of around 350C. microPET images were reconstructed with the ordered-subsets expectation-maximization algorithm (OESM)(21 (link)) using 16 subsets and 4 iterations. Attenuation correction was not performed.
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3

PET Imaging of Lymphoma Xenografts

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PET imaging of SU-DHL-6–bearing mice was performed using 89Zr-labeled L804-ofatumumab (6.66 MBq) at 1, 2, 3, and 7 d after injection (R4 microPET; Siemens). A blocking cohort with 200 μg of unlabeled ofatumumab (2 h before tracer) was included. The scanner was calibrated with a mouse-sized cylinder phantom of aqueous 18F with a known activity concentration (25 (link)), energy windows of 350–650 keV, and coincidence timing of 6 ns. Corrected scanner data were reconstructed by an iterative 3-dimensional maximum a priori algorithm. Volumes of interest were defined, and %IA/mL was computed (ASIPro; Siemens).
PET/CT of the SU-DHL-6 tumor–bearing animals was performed on the Nanoscan (Mediso) on day 7. A CT acquisition of 720°, 70 kV/980 μA of 90 ms, and 4× binning was reconstructed by filtered backprojection to produce isotropic 124-μm voxels (122 × 122 × 97 mm). PET data (400–600 keV, 5-ns timing) were reconstructed using the iterative, 3-dimensional TeraTomo algorithm (4 iterations and 6 subsets; Mediso Medical Imaging Systems). Decay, attenuation, and scatter corrections were applied to quantify injected activity.
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4

Multimodal Imaging of Sigma-1 Receptors

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All animals were anesthetized with humidified, oxygen-enriched 2-3% isoflurane (inhalation). The animal was secured in a transportable holder with fixed firm padding to eliminate motion between PET and MRI scans while allowing it to breathe 2-3% isoflurane via a nose cone fixed to the animal holder. Fiducial markers made with a diluted [18F]FTC-146 solution (30 µCi/mL) in longitudinal plastic tubes placed across the bottom of the animal holder were utilized for assistance in PET and MRI image co-registration. The animals underwent sequential PET (microPET R4; Siemens Medical Solutions) and MRI (a self-shielded 30-cm-bore 7-T magnet [Varian] with a 9-cm-bore gradient insert [Resonance Research Inc.] using EXCITE2 electronics and the supporting LX11 platform [GE Healthcare]) using dedicated small animal imaging instruments. For PET imaging, 1000 µCi (37 MBq) [18F]FTC-146 was injected via tail vein, and a 10 min static scan of the thighs was obtained 30 min post-injection. For MRI, T1 Fast Spin Echo images (TR 800 ms; TE 7.7 ms; slice thickness 1 mm; in-plane resolution 234 µm2) were obtained of the rat thighs. Haloperidol (1.6 mg/kg), a widely used S1R blocker, was given intravenously 30 min prior to tracer administration for the blocking studies.
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5

In Vivo Molecular Imaging of Tumors

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Mice were divided into imaging and control groups (n = 4 mice). To analyze tumor imageability after intratumoral delivery, mice received an intratumoral injection of 104 PFU per tumor of either CF33-hNIS, CF33-Fluc, or PBS when tumors reached 100 mm3. At 7, 15, and 22 days post-viral infection, mice in each group received 200 μCi of I-124 injected per tail vein. The radioisotope was obtained from the City of Hope Small Animal Imaging Core Radiopharmacy. PET imaging was then obtained 2 h following injection using the small-animal PET scanner (microPET R4; Siemens Corporation), which provides fully three-dimensional PET imaging with spatial resolution of better than 2.0 mm and quantitative accuracy for measurement of tissue activity concentration on the order of 10%. The 8-cm axial field of view is adequate for simultaneous whole-body imaging of mice. Advanced image reconstruction software provides resolution approaching 1.0 mm. Quantitative accuracy is supported by scatter, dead time, and measured attenuation corrections. The system includes a fully developed image analysis package that supports volumetric regions of interest and fusion of PET with co-registered anatomic CT. In order to protect mouse thyroids from radioiodine ablation, all mice received T4 supplementation with 5 mg levothyroxine/L of water beginning 1 week prior to radioiodine administration.
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