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Crc 15 pet

Manufactured by Mirion Technologies
Sourced in United States

The CRC-15 PET is a radiation detection device used for measuring and monitoring radioactivity levels. It is designed to measure positron emission tomography (PET) radioactive isotopes. The CRC-15 PET provides accurate and reliable measurements of radioactivity in various applications.

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4 protocols using crc 15 pet

1

Radiosynthesis and PET Imaging of [19F]FTC-146

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Unless otherwise stated, chemicals were purchased from commercial sources and used without further purification. BD1047 for mice studies was purchased from Sigma Aldrich. [19F]FTC-146 (99.1 % chemical purity) reference compound was provided by Albany Molecular Research Inc. (Albany, NY). Radiochemistry and semi-preparative high performance liquid chromatography (HPLC) was performed using a TRACERlab FX-FN module (GE Healthcare) with an ancillary HPLC pump (Dionex P680) and UV detector (KNAUER K-2001). Analytical HPLC was performed on a quaternary pump (Agilent 1200 series) equipped with an autosampler, a photodiode array UV detector, and a model 105S single-channel radiation detector (Carroll & Ramsey Associates). Radiotracer doses for animal studies were measured using a dose calibrator (Capintec, CRC-15 PET). Positron emission tomography/computed tomography (PET/CT) imaging of mice was performed using microPET/CT hybrid scanner (Siemens Inveon). All PET data were reconstructed using a 3-dimensional ordered subsets expectation maximization algorithm (16 subsets, 4 iterations) with scatter and dead time correction, and a matrix size of 128 × 128 × 159. Attenuation correction was applied to dataset from CT image.
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2

18F-FDG PET/CT Patient Preparation

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The patients were made to change to hospital robe and given instruction on sitting quietly and calmly postinjection. 18F-FDG activity was dispensed with respect to the patient's weight and the Group allotted and measured using dose calibrator (CRC-15PET, Capintec Inc., USA). The administered dose and time were noted in the datasheet. These patients were seated in their respective postdose administration waiting areas. During the waiting period, the patients were advised to drink approximately a liter of water mixed with oral contrast and instructed to void in the radioactive toilet.
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3

Multimodal Imaging of NPs and Cells

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Fe3O4@Al(OH)3 NPs containing 4.3 µg of iron were labeled with 10 MBq [18F]NaF, while 106 mMSC plated the day before where labeled with NPs containing 21.4 µg of iron in 1 mL of saline (end concentration of iron on cells = 0.38 mM) and radiolabeled with 30 MBq [18F]NaF. For imaging purposes, serial dilutions of these NPs and cells were resuspended in equal amounts of saline and 2% agar (microbiology grade; Sigma-Aldrich; diluted in distilled water) in 200 µL Eppendorf tubes. The following controls were used: (1) equal amounts of saline and 2% agar, and (2) 5 × 104 unlabeled mMSCs in saline and agar. The radioactivity present in the samples was measured using a dose calibrator (CRC-15 PET, Capintec Inc., Ramsey, NJ, USA). The tubes were then placed into a cylindrical in-house made Teflon holder (outer diameter = 7 cm, inner diameter = 3.5 cm) filled with 2% liquid agar. For more details on this phantom, see Trekker et al. [35 ]. After agar solidification, the phantom was scanned using PET/MRI. Three MRI measurements were performed per phantom.
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4

Ex Vivo Quantification of 52Mn Biodistribution

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Ex vivo quantification of 52Mn activity in each injected dose, in the urine, and in the feces were determined using a Capintec CRC-15PET dose calibrator. Injected dose activity was determined from the difference in activity recorded in the loaded syringe and injection line prior to and after injection. Quantification of Mn-52 activity in ex vivo tissue samples was performed using a Perkin Elmer 2480 Wizard2 gamma counting system. Percentage injected (%ID) dose in ex vivo tissue samples was determined by comparing tissue counts to a measured aliquot of the injected dose. Bone, blood, fat, and muscle were estimated to account for 13%, 7%, 13%, and 40% of the total body weight. All measurements were corrected to account for decay. Limit of quantification (LOQ) was defined as 3 SD above the mean background counts per minute.
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