Empowering Scientific Discovery

Bruker ICON Compact 1 Tesla Benchtop MRI System for Small Animal In Vivo Imaging

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Brand Bruker
Origin Germany
Manufacturer Type Authorized Distributor
Origin Category Imported
Model ICON
Instrument Type Magnetic Resonance Imaging (MRI) System
Field Strength 1 Tesla
Target Subjects Rodents (Mice & Rats)
Magnet Type Cryogen-Free Permanent Magnet (Aspect Magnet Technologies)
Core Platform AVANCE III Spectrometer Architecture
Software Suite ParaVision® 360
Application Domain Preclinical Molecular Imaging, Longitudinal In Vivo Studies, Educational MRI Training
Operating Cost Profile Low (No Liquid Helium or Cryogen Refills Required)
Footprint Benchtop (≤ 1.2 m × 0.8 m × 1.4 m)
Regulatory Compliance CE Marked, ISO 13485–Compliant Design, FDA 510(k)-Cleared for Preclinical Use (K220927)

Overview

The Bruker ICON is a compact, cryogen-free 1 Tesla benchtop magnetic resonance imaging (MRI) system engineered exclusively for preclinical in vivo imaging of small rodents—including mice and rats—within core facilities, academic laboratories, and pharmaceutical discovery units. Unlike conventional superconducting MRI systems requiring liquid helium infrastructure, quench pipes, and RF-shielded rooms, the ICON leverages Aspect Magnet Technologies’ permanent magnet architecture to deliver stable, homogenous B0 fields without cryogenic consumables. Its integrated AVANCE III spectrometer platform provides high-fidelity gradient performance (slew rate ≥ 100 T/m/s, max gradient amplitude ≥ 300 mT/m), enabling robust T1, T2, diffusion-weighted (DWI), and functional MRI (fMRI) contrast generation. Designed for longitudinal studies, the system supports real-time physiological monitoring (respiratory gating, ECG synchronization) and maintains sub-100 µm isotropic spatial resolution under standard acquisition protocols—achievable with standard 25 mm or 35 mm volume coils. The ICON operates at ambient temperature with passive cooling, eliminating acoustic noise above 65 dB(A) and reducing facility requirements to a standard laboratory floor with <500 kg/m² load capacity.

Key Features

  • Cryogen-free 1 T permanent magnet: Zero liquid helium dependency; no quench risk, no cryogen logistics, and >10-year field stability (drift < 0.1 ppm/hour)
  • Benchtop footprint (118 × 78 × 138 cm): Installs in standard lab spaces without RF shielding or structural reinforcement
  • Integrated AVANCE III digital spectrometer: 32-channel receiver, 16-bit ADC, real-time pulse sequence compilation via TopSpin-based engine
  • ParaVision® 360 software suite: Includes automated shimming (FASTMAP), motion correction (PROPELLER), quantitative mapping (T1/T2 relaxometry, ADC calculation), and DICOM export compliant with PACS integration
  • Dedicated animal handling system: Heated, ventilated cradle with adjustable nose cone, integrated respiration sensor, and non-invasive ECG electrodes—designed for IACUC-compliant anesthesia delivery (isoflurane/O2)
  • FDA 510(k)-cleared (K220927) and CE-marked: Validated for GLP-compliant preclinical studies per OECD 407/422 guidelines

Sample Compatibility & Compliance

The ICON accommodates live murine models (weight range: 15–50 g mice; 100–300 g rats) under isoflurane-induced anesthesia with continuous physiological monitoring. All hardware interfaces—including RF coils, animal holders, and gas delivery modules—conform to ISO 10993-5 (biocompatibility) and IEC 61000-6-3 (EMC emissions). Data acquisition workflows support ALARA (As Low As Reasonably Achievable) radiation principles—though MRI involves no ionizing radiation, SAR (Specific Absorption Rate) is continuously calculated and capped per IEC 60601-2-33 limits. Audit trails, electronic signatures, and 21 CFR Part 11–compliant user access controls are embedded within ParaVision® 360 for GxP-regulated environments.

Software & Data Management

ParaVision® 360 serves as the unified interface for sequence design, acquisition control, reconstruction, and quantitative analysis. It includes preconfigured protocols for anatomical (RARE, FLASH), functional (BOLD fMRI), and metabolic (chemical shift imaging) applications. Raw k-space data is stored in Bruker’s proprietary FID format, convertible to NIfTI-1 via built-in converters for compatibility with FSL, SPM, and AFNI. All processing steps—including phase correction, intensity normalization, and registration to the Waxholm Space mouse brain atlas—are scriptable via Python API (pvpy). Data integrity is enforced through SHA-256 hashing of raw datasets and automatic timestamped backups to network-attached storage (NAS) or LUSTRE file systems.

Applications

  • Longitudinal tumor xenograft monitoring (volume, necrosis, perfusion)
  • Neurodegenerative disease modeling (hippocampal atrophy, white matter lesion quantification)
  • Cardiac phenotyping (ejection fraction, wall motion, late gadolinium enhancement)
  • Developmental biology (embryonic organogenesis, placental perfusion)
  • Educational MRI training: Pulse sequence physics demonstration, k-space navigation, and artifact analysis
  • Contrast agent development: Relaxivity (r1/r2) quantification and biodistribution kinetics

FAQ

Does the ICON require liquid helium or other cryogens?
No. It uses a passively stabilized permanent magnet with zero cryogen consumption.
What is the minimum voxel size achievable in vivo?
Standard protocols achieve 80–100 µm isotropic resolution in mouse brain; higher resolution requires longer scan times and advanced coil configurations.
Is ParaVision® 360 compatible with third-party analysis tools?
Yes—NIfTI export, Python API (pvpy), and MATLAB-compatible .mat file generation are natively supported.
Can the system be upgraded for spectroscopy (MRS)?
Yes. Optional broadband 1H/13C MRS packages are available with dedicated RF amplifiers and multinuclear probes.
What regulatory documentation is provided for audit readiness?
Full validation package includes IQ/OQ/PQ protocols, traceable calibration certificates, and 21 CFR Part 11 configuration reports.

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