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Clinscan system

Manufactured by Bruker
Sourced in Germany

The ClinScan system is a compact nuclear magnetic resonance (NMR) spectrometer designed for clinical research applications. It provides high-resolution NMR analysis of a variety of biological samples, including blood, urine, and tissue extracts. The ClinScan system is capable of performing advanced metabolic profiling and small molecule identification to support clinical research studies.

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9 protocols using clinscan system

1

Quantifying Tumor Burden via 7T MRI

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After adeno-Cre instillation, tumors were monitored via MRI and when tumor burden was measurable, mice were placed on one of four arms of a treatment regimen. Animals were anaesthetized via inhalation of isoflurane and kept warm on heated waterbed, vitals were monitored via cardiac and respiratory cycle (SA instruments), and recorded every 10 minutes while the animal was under anesthesia. The SA instruments pneumatic respiratory monitor was used to remove breathing artifacts by gating on the respiratory cycle. The Bruker ClinScan system used to scan the animals had 12 cm of actively shielded gradients, maximum strength 630 mT/m, and a slew rate of 6,300 T/m/second. This instrument is a 7T system with 2 × 2 array coil and 2D gradient echoT1-weighted sequences. The parameters used for imaging are as follows: 18 slices, TR = 170 ms, TE = 2.4 ms, α = 38°, Navg = 3, FOV 26 × 26 mm2, 1 mm thickness, matrix size 256 × 256, for a voxel size of 0.102 × 0.102 × 1.0 mm. In 2021, the system was upgraded to a Bruker Biospec system. For this upgraded machine, the Bruker IntraGate software was used to remove respiratory and cardiac motion with parameters: 18 slices, TR = 8.96ms ms, TE = 3.4 ms, α = 10°, oversampling = 28, FOV 26 × 26 mm2, 1 mm thickness, matrix size 192 × 192, 10 minutes. Models were then built on Slicer three-dimensional (3D) software to calculate tumor volume.
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2

Cardiac Cine MRI Acquisition Protocol

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CMR was performed on a 7-Tesla Bruker ClinScan system (Bruker, Ettlingen, Germany) equipped with a 2 × 2 hydrogen phased-array coil and a gradient system (strength: 450 mT/m; slew rate: 4500 T/m/s). Cine images were acquired using a black-blood gradient echo imaging technique (14 (link)). Relevant acquisition parameters included: 14 phases per cardiac cycle, repetition time (TR) 8.2 ms, echo time (TE) 1 ms, averages 1, field of view (FOV) 50 × 50 mm, pixel size 0.357 × 0.357 mm, slice thickness 1.3 mm. We acquired 4–5 short-axis images and 2 long-axis images for each mouse. The long-axis images consisted of a standard apical 4-chamber view and a 2-chamber view perpendicular to the 4-chamber view. The short-axis images were planned perpendicular to the 4-chamber long-axis image.
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3

Cardiac MRI Protocol for Mouse and Human Imaging

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All mouse imaging was performed on a 7 T Bruker ClinScan system (Bruker, Ettlingen, Germany) equipped with a 4-element phased array cardiac coil. Short-axis images (basal, mid-ventricular, apical) and long-axis images (two and four-chamber) were acquired with 13–20 frames per cardiac cycle. In-plane displacements were encoded for each image. Acquisition parameters were: TR = 7.4 ms, TE = 1.0 ms, Acquisition Matrix = 128 × 128, Pixel Spacing = 0.25 mm, Slice Thickness = 1 mm, Flip Angle = 20°, 36 inter-leaved spirals, displacement encoding frequency (ke) =1.0 cycles/mm.
Human subject imaging was performed on either a 3 T Siemens Tim Trio or 1.5 T Siemens Avanto system (Siemens Healthcare, Erlangen, Germany) with a 6-element phased array cardiac coil and a 24-element spine coil. Short-axis images (basal, mid-ventricular, apical) and long-axis images (two and four-chamber) were acquired with 17–28 frames per cardiac cycle. In-plane displacements were encoded for each image. Acquisition parameters were: TR = 17 ms, TE = 1.1 ms, Acquisition Matrix = 128 × 128, Pixel Spacing = 2.6 – 2.8 mm, Slice Thickness = 8 mm, Flip Angle = 20°, 6 inter-leaved spirals, ke = 0.1 cycles/mm.
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4

Magnetic Relaxometry of Engineered SPIONs

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T2 relaxometry was performed using a 7.0 T Bruker ClinScan system. The instrumental parameters were set as follows: a 7.0 T magnetic field strength, pixel spacing at 0.297/0.297, repetition time 2000 ms, echo time 11 ms, and slice thickness of 2 mm. Synthesized SPIONs and their modification SPIONs@PAMAM and SPIONs@FA-PAMAM were analyzed at different iron concentrations 10, 20, 40, 60, 80, and 100 μg/mL. The T2 relaxivity was calculated from the linear slope of the inverse T2 (1/T2) relaxation time according to the iron concentration.
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5

Murine Brain Imaging Using 7T MRI

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The animal MRI study was performed using a 7T Bruker ClinScan system (Bruker BioSpin MRI GmbH, Germany) equipped with a 12 S gradient coil. A mouse head volume coil (Bruker BioSpin) was used. Animals were anesthetized and maintained with 1.5–2% isoflurane during the experiments. Transverse T2-weighted turbo spin echo images were acquired for volume measurements (Repetition time/Echo time = 3660/50 ms, field of view = 25 × 25 mm, matrix = 320 × 320 pixels, number of averages = 1, thickness = 0.4 mm, scan time = 11.5 min).
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6

Cardiac MRI Assessment of Post-Infarction Remodeling

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Cardiac magnetic resonance imaging (CMR) was performed on a 7-Tesla ClinScan system (Bruker, Ettlingen, Germany, http://www.bruker.com) equipped with a 4-element phased-array cardiac coil and a gradient system with a maximum strength of 450 mT/m and a maximum slew rate of 4500 mT/m/s. We acquired whole short-axis stack images from base to apex for comparison with late enhancement images. The short-axis images were planned perpendicular to the four-chamber long-axis image. For late gadolinium-enhanced magnetic resonance imaging, a 0.6 mmol/kg bolus of gadolinium-diethylenetriamine pentaacetic acid (Gd-DTPA; Gadavist, Bayer Health Care, Whippany, NJ) was injected using the intraperitoneal route. Imaging was initiated 10 min after the injection of Gd-DTPA using an electrocardiographically gated segmented magnetization-prepared fast low-angle shot sequence with a fixed inversion time at 500 ms. CMR was performed at D3 and D14 post-MI. The CMR data were analyzed using commercially available post-processing software: CMR42 (Circle Cardiovascular Imaging, Calgary, Alberta, Canada, http://www.circlecvi.com) and ImageJ (NIH). Infarct length was calculated as a percentage of left ventricular length. All analyses were performed by blinded investigators.
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7

Volumetric Brain Analysis in Mice

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At least 5 mice of each genotype (age P40–60) were used for volumetric analyses. MRI study was performed using a 7 T Bruker ClinScan system (Bruker BioSpin MRI GmbH, Germany) equipped with 12S gradient coil. A 2-channel surface coil was used for MR imaging. Animals were anesthetized and maintained with 1.5% isoflurane during MRI sessions. Transverse T2-weighted turbo spin echo images were acquired for volume measurements (TR/TE = 3660/50 ms, FOV = 25 × 25 mm, matrix = 320 × 320, NEX = 1, thickness = 0.4 mm, scan time = 6.5 min). Total brain volumes were obtained by manually segmenting brain regions from olfactory bulbs to cerebellum, and computing volumes using OsiriX (Pixmeo, Switzerland). Each data point in the graph represents 1 mouse.
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8

Noise-Induced Hearing Loss Imaging

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Animals (n = 15) were imaged 48 hours after noise-exposure. Isoflurane was administered (5% for induction and 2% for maintenance) with room air as the vehicle to immobilize the animals during imaging. For the duration of the scan, animals with no silicone ear plugs, were placed and remained on a heated re-circulating water pad to maintain body temperature. High-resolution MRI scans were acquired using a 7 T Bruker Clinscan system with a receive-only 4 element coil array centered on the animal’s head. Single spin-echo (echo time [TE] 11 ms; 20 × 20 mm2, matrix size 192 × 192; slice thickness 400 µm; in-plane resolution 104 μm) images (23) were acquired at different repetition times (TRs) in the following order (number of scans per TR in parentheses): 0.15 second (6), 3.50 seconds (1), 1.00 seconds (2), 1.90 seconds (1), 0.35 second (4), 2.70 seconds (1), 0.25 second (5), and 0.50 second (3). To compensate for reduced signal-noise ratios at shorter TRs, progressively more images were collected for averaging as the TR decreased. Rostral and caudal MRI T1 maps of the cochlea were obtained from animals in each experimental group (Fig. 4a). Rats were allowed to regain consciousness after MRI examination.
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9

Cardiac MRI Imaging in Mice

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MRI studies were conducted under protocols that comply with the Guide for the Care and Use of Laboratory Animals (NIH publication no. 85-23, Revised 1996). Mice were positioned in the scanner under 1.25% isoflurane anesthesia and body temperature was maintained at 37°C using thermostatic circulating water. A cylindrical birdcage RF coil (30 mm-diameter, Bruker, Ettlingen, Germany) with an active length of 70 mm was used, and heart rate, respiration, and temperature were monitored during imaging using a fiber optic, MR-compatible system (Small Animal Imaging Inc., Stony Brook, NY). MRI was performed on a 7 Tesla (T) Clinscan system (Bruker, Ettlingen, Germany) equipped with actively shielded gradients with a full strength of 650 mT/m and a slew rate of 6666 mT/m/ms 60 . Six short-axis slices were acquired from base to apex, with slice thickness of 1 mm, in-plane spatial resolution of 0.2 × 0.2 mm 2 , and temporal resolution of 8-12 ms. Baseline ejection fraction (EF), end-diastolic volume (EDV), end-systolic volume (ESV), myocardial mass, wall thickness, stroke volume (SV), and cardiac output (CO) were assessed from the cine images using the freely available software Segment version 2.0 R5292 (http://segment.heiberg.se).
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