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Omniscan

Manufactured by Takeda Pharmaceuticals
Sourced in Norway

Omniscan is a contrast agent used in medical imaging procedures. It is designed to enhance the visibility of certain structures and organs during imaging tests such as magnetic resonance imaging (MRI) or computed tomography (CT) scans. The core function of Omniscan is to improve the diagnostic capabilities of these imaging techniques by providing clearer visual information.

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3 protocols using omniscan

1

Gadolinium-Enhanced MR Angiography Protocol

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All MR angiography was performed with the 1.5 T MRI system (Sonata, Siemens HealthCare, Erlangen Germany) using a 8-channel neurovascular array coil (Siemens HealthCare, Erlangen Germany). The parameters were as follows: Field of view, 39 cm; TR/TE, 4.3/1.31 ms; flip angle, 30°; matrix, 202 x 384; number of average, 1; section thickness, 1mm; no interslice gap. A total of 72 slices were acquired and the acquisition time was 17 seconds. A bolus of 15 ml of gadodiamide at a concentration of 0.5 mmol/ml (Omniscan, Nycomed, Princeton, NJ) was injected at 2 ml/s with a flush of 15 ml of saline at the same rate, using a power injector (Medras, Medrad, Indianola, PA). Two phases of pre-contrast and arterial phase were obtained. And, only the arterial phase images were displayed on picture archiving and communication system (PACS), using 3D maximum-intensity-projection (MIP) reconstruction.
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2

Intracranial Metastases Evaluation via MRI

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For more precise in vivo evaluation of intracranial metastases formation, cranial MRI (cMRI, 9.4 T, Bruker Topspin 9/20) after Gadolinium contrast administration was performed on day 26 after intracardial tumor cell injection. Mice were sedated with 3% isoflurane and kept under anesthesia at 0.5–1.5%. Constant body temperature was maintained at 37 °C by a heating plate. During imaging respiration was surveilled using an external breathing surface pad (in house development, LabVIEW program, National Instruments Corporation). A dose of 0.2 mmol/kg i.v. gadodiamide (Omniscan; Nycomed) was given to each animal and standard T1-w and T2-w images were acquired. For quantification of tumor volumes, tumors were manually segmented on T1-w images using the Fiji software (general public license) [28 (link)].
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3

DCE-MRI Imaging of Head and Neck Cancer

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In our study, all subjects were recruited from The First Affiliated Hospital, Sun Yat-sen University. DCE-MRI was performed on a 3.0-T system (Magnetom Trio, Siemens) with field of view (FOV) of 22 × 22 × 6 cm (AP × RL × FH), a flip angle of 15°, and scanning time of 6 minute 47 seconds with 65 dynamic scans, 5.9 seconds per scan. The contrast agent gadodiamide Gd-DTPA (Omniscan; Nycomed, Oslo, Norway) was injected intravenously as a bolus into the blood at around the 8th dynamic acquisition using a power injector system (Spectris; Medrad, Indianola, Pennsylvania), immediately followed by a 25-mL saline flush at a rate of 3.5 mL per second. The dose of Gd-DTPA was 0.1 mmol/(kg body weight) for each patient. The reconstructed DCE-MRI images were a 4D matrix (144 × 144 × 20 × 65) with 20 slices.
One hundred and twenty samples of DCE-MRI images containing the HNC tumor lesions were used as our database. Each sample was the DCE-MRI time series of a slice and thus was a 144 × 144 × 65 matrix. Eighty samples were selected randomly as the training dataset while the remaining 40 samples were the testing dataset to verify the accuracy of segmentation.
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