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3 t mr750 system

Manufactured by GE Healthcare

The GE Healthcare 3 T MR750 system is a magnetic resonance imaging (MRI) scanner that operates at a field strength of 3 Tesla. It is designed for clinical diagnostic imaging applications.

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4 protocols using 3 t mr750 system

1

Multiparametric MRI for Prostate Imaging

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Patients underwent prostate MRI on a 3 T MR750 system (GE Healthcare, Waukesha, WI) using a 32-channel receiver coil. Intravenous injection of hyoscine butylbromide (Buscopan, 20 mg ml−1; Boehringer Ingelheim, Ingelheim am Rhein, Germany) was administered prior to imaging unless clinically contraindicated. Multiparametric MRI protocol included axial T1 weighted imaging, multiplanar high-resolution T2 weighted two-dimensional (2D) fast recovery fast spin echo (FSE), spin-echo echoplanar imaging pulse diffusion-weighted imaging (DWI), and dynamic contrast-enhanced (DCE) imaging, as described previously.25 (link)
DWI was performed with b-values: b-150, b-750, and b-1,000; with additional small field of view DWI obtained using b-2,000s/mm2; ADC maps were automatically calculated. Follow-up studies did not include post-contrast DCE sequences, but the protocol was otherwise identical for all patients and all scans included in the analysis.
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2

Structural Brain Imaging with 3T MRI

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All scanning was conducted on a General Electric 3T MR750 System (General Electric Healthcare, Milwaukee, WI) with Twin Speed gradients and a GE 8-channel head coil at the Center of Functional MRI at UCSD. See the supplement for more details.
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3

Multimodal MRI Imaging Protocol for Brain Evaluation

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All MRI data were acquired on a 3T MR750 system (GE Healthcare, Milwaukee, WI) using a 16-channel head, neck, and spine array coil. The multimodal MRI protocol included a pre-contrast T1-weighted fast spoiled gradient echo (FSPGR) sequence (T1w), a T2-weighted PROPELLER sequence (T2w), and a fluid-attenuated inversion recovery (FLAIR) sequence which were followed by a gadolinium (Gd)-enhanced T1-weighted FSPGR sequence (T1c). All imaging parameters are shown in Table 2.

MR sequence parameters

3D QTIT1-weighted FSPGR (T1w)Gd-enhanced T1-weighted FSPGR (T1c)T2-weighted PROPELLER (T2w)CUBE FLAIR (FLAIR)
Acquisition3D3D3D2D3D
Native resolution (mm3)1.125 × 1.125 × 1.1250.47 × 0.47 × 0.80.47 × 0.47 × 0.80.5 × 0.5 × 3.30.8 × 0.47 × 0.47
Matrix size200 × 200 × 200512 × 512 × 212512 × 512 × 212512 × 512 × 46192 × 512 × 512
Field of view (mm3)225 × 225 × 225240 × 240 × 170240 × 240 × 170260 × 260 × 152154 × 240 × 240
Slices---46-
Native slice thickness (mm)---3.0-
TE (ms)1.82.12.1120.792
TR (ms)7.84.67.157515002
TI (ms)18---1701
ɑ (°)0.8 ≤ ɑ ≤ 70121216090
Acquisition time (min)6:251:544:435:154:48
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4

Quantifying CAR-T Cell Cytotoxicity and Detection

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To compare the cytotoxicity of PFC + and unlabeled CAR-T cells, 5 × 104 NALM6-tdT-FLuc cells were seeded with PFC + or unlabeled CAR-T cells at increasing effector to target ratios (1:4, 1:2, 1:1). Twenty-four hours later, 1 µL of D-luciferin was added to each well (30 mg/ml, Syd Labs), and BLI was performed immediately on an IVIS Lumina XRMS scanner (IVIS Lumina XRMS In Vivo Imaging System, PerkinElmer). BLI signal was evaluated with region-of-interest (ROI) analysis using Living Image Software (PerkinElmer). Quantification was performed by drawing ROIs over each well to obtain the average radiance per well (photons/second/mm2/steradian).
To evaluate the minimum number of PFC + CAR-T cells that could be detected at 3 T, triplicates of CAR-T cell pellets containing decreasing numbers of labeled cells (2, 1, 0.5, 0.25, 0.1 (× 106) cells) were imaged using 19F MRI. Samples were made by mixing labeled and unlabeled CAR-T cells to obtain a total of 2 × 106 cells per Eppendorf tube; the Eppendorf tube was then spun down to form pellets and then covered with 1% agarose prior to MRI. The resulting samples were imaged at 3 T using a clinical GE 3 T MR750 system following the same imaging protocols used for in vivo imaging (see below). Analysis of all 19F MRI images is described further below.
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