McKnight Brain Institute, LG-114
This Philips whole-body 3 T MRI scanner features a 70 cm bore and includes the latest acquisition techniques for human MRI research, including multinuclear capabilities, functional MRI (fMRI) and advanced diffusion imaging (dMRI), and magnetic resonance elastography (MRE), spectroscopy (MRI/S), whole-body scanning and much more. The extra space better accommodates in-bore equipment, like the Resoundant probe for MR elastography studies of the liver. The magnet provides the largest homogenous field-of-view, 55 cm, in a commercial 70 cm system while still providing strong gradients. The Elition is equipped with Philips’ unique broadband digital MR architecture, the d-STREAM, which samples the signal directly at the coil and transmits the signal through fiber optics to reduce noise and increase SNR. The system comes with the latest technologies for neuro, cardiac, MSK, liver, and whole-body imaging including, compressed SENSE technology, and numerous RF coil and pulse sequence packages for advanced MR imaging and spectroscopy research.
The scanner is operated by accredited, licensed and experienced MRI technologists.
System Console Model: Ingenia Elition 3T X / 70 cm
Software Release: R5.6.1 and R5.6.0 (Multinuclear)
- Working bore diameter of 70 cm
- High-performance gradient system for 70 cm bore (45 mT/m @ 220 T/m/)
- Philips d-stream RF architecture sampling signals directly at the RF coils to reduce noise and increase SNR
- 55 x 55 x 50 cm3 field of view
- Multinuclear capabilities
- Application packages for neuro and whole-body imaging, including cardiac, angiography, MSK, fMRI, dMRI, and spectroscopy
- Compressed SENSE technology for high speed, high quality images with high SNR
- MR elastography equipment from Resoundant Inc.
- Body coil – 2 element quadrature design coil. Quadrature transmit B1 is 13.5 mT peak except for Multi-Band SENSE where amplitude is increased to 20 mT.
- Head 3.0 T – 15 elements head or up to 51 elements total spine
- HeadNeck – 20 elements head/neck or up to 52 elements Head neck spine
- TotalSpine – 44 elements if imaging spine w/o anterior head or NV attachment
- T/R Head- single element transmit / single element receive *T/R Interface
- Head 32ch – 32 elements
- Torso 3.0T – 32 elements
- Flex M 3.0T – 6 elements
- Flex L 3.0T – 8 elements
- dKnee 16 – 16 elements
- Small Extremity 16ch – 16 elements
- Expansion WholeBody: Includes 2nd anterior Torso coil for total body imaging up to 108 elements with 200 cm coverage
- Infant (Pediatric) head, neck and torso coils
The following 3rd party coils are available for research use. Interested users should contact Dr. Jens Rosenberg.
- Rapid Biomedical quad 1H/31P volume coil (Ø = 26.5 cm)
- 31P linear surface coils from Philips and PulseTech
The following Patches are available for research use. Interested users should contact Dr. Jens Rosenberg.
- CEST patch (in process)
- Multidimensional diffusion (in process)
Users are responsible to retrieve their data immediately after the data has been collected. With the limited storage space on the workstation it is not guaranteed that the data will be available longer than 48 hours after the data is collected. Any external hard drive can be used, included encrypted drives that does not require software to be installed on the workstation.
Visual Projection System
For visual presentation, the scanner is equipped with a BOLDscreen 32 from Cambridge Research Systems. featuring a 32″ 1920×1080 IPS LCD panel with native 10-bit RGB color resolution and a contrast ratio of 1400:1 (measured with the backlight on; [1 1 1]:[0 0 0] RGB contrast ratio). The panel features 120 Hz panel drive capability, and a fast 5 ms grey-to-grey response time. The digital video input box (AVI) will synchronize to a 1920×1080 @ 120 Hz video signal and will output video at the same rate. The BOLDscreen 32 AVI supports inputs at other resolutions and frame rates, including from sources like iPads and Internet streaming media players. Users can connect to the AVI box with a computer equipped with a DisplayPort or HDMI connection.
Subject Response System
To complement the stimulus presentation equipment, an MRI compatible fiber-optic response gathering system is also supplied. The response system is from Current Designs and features automatic handheld device identification, optical triggering and 32 channels with automatic gain adjustment and response device identification.
The primary output for most users is the full-speed USB output, which simplifies interfacing to any hardware or program, and RS-232 serial and TTL parallel outputs are also available for special interfacing needs and for support of older programs and computers. Currently available response devices are 2-button, 8-button, scroll click, and trackball devices.
MRI-compatible equipment for physiological measurements is available from BioPac, Inc. The BioPac equipment consist of three modules able to measure ECG, SpO2 and blood pressure. Users can attach additional modules to this unit at their own expense. All consumables associated with the BioPac (wipes, ECG leads, gel, etc.) must be provided by each individual research group. A list of consumable products can be found below together with respective product number for easy ordering. This is shared equipment between both the Philips Elition and Siemens Prisma scanners. Please contact Dr. Rosenberg for further information.
Four examination rooms are available for subject screening and preparation. Two of the examination rooms, LG-110E and LG-110A are for Philips and Siemens respectively and are reserved one hour prior to the scheduled MRI exam. The other two (LG-110D and LG-110B) can be pre-booked if more time is needed for subject preparation. Two waiting areas are also provided where researchers and individuals accompanying the participants (e.g., parents and/or guardians) may wait. There is also space provided where participants can change into scrubs or other MRI appropriate clothing. A room with limited storage space for individual research group owned MRI equipment is also available.
Booking, Rate and Cancellations
Booking can be made continuously on a first come-first-serve basis using the online booking system after a billing code has been set up with the AMRIS Facility. To set up a billing code please contact Cynthia Sager. If available, the requested time will be scheduled. Otherwise, a 3 T staff member will contact the requester to schedule an alternate time. It is highly recommended that the user checks the 3 T Elition calendar prior to submitting a time request to make sure the desired time is available. Submitting requests to “place-hold” and for “defensive booking” are not allowed, but the Facility will work with investigators who need to regularly schedule reservations when they have a subject or experiment planned.
Cancellations for prime-time hours between 8 am to 2 pm must be made 1 week prior to the scheduled exam. All other times must be cancelled 48 hours prior to the scheduled exam. Any cancellations within the one week (for 8 am to 2 pm reservations) or 48 hours (for other times) before the scheduled exam time will be charged at the hourly rate for the reserved time unless another billable study can make use of the time.
- 8 am – 8 pm Monday through Friday: $500 / hour
- All other times with no staff: $350 / hour
- All other times with staff: $ 500 / hour
- Commercial (for-profit) scanning: $1500 / hour
To obtain access to the AMRIS facility, all personnel must attend an AMRIS Facility general magnet safety class held monthly by Dr. James Collins. In addition, a 3 T magnet specific online safety training is needed for access to the 3 T facility (under development).
For any new study (new billing code), two hours of protocol development time is allowed on the scanner, free of charge. Investigators should discuss their project with Dr. Rosenberg to review their needed protocol and make sure the required instrumentation, techniques and sequences are available, and that sufficient protocol development and/or validation time is allocated. If necessary, Dr. Rosenberg can assist in developing an imaging protocol based on specific needs of a project; it is important to realize that optimizing a specific protocol for a particular project is critical to obtaining significant data. If the development is more involved than can be accomplished by refining Philips product sequences and/or it involves significant technical development, the investigator(s) must fund Dr. Rosenberg’s time from their project budget and/or include Dr. Rosenberg in the project as a co-investigator.
Instrument Time for Protocol Development
- For pilot studies to acquire preliminary data, there are several funding mechanisms available through the MBI, CTSI, and SECIM programs at UF.
- For grant proposals to external funding agencies that need MR techniques and protocols not already available on our scanner and will require Dr. Rosenberg’s time to develop them, the grant application budget must include any funds needed for acquisition of the hardware and/or software and funds to support Dr. Rosenberg’s time developing the protocols.
- If the hardware and/or necessary MR protocols or sequences required for a project are not already available in the AMRIS Facility and would be of interest to the larger 3 T user group, requests may be made to Dr. Rosenberg, Dr. Long and Dr. Mareci for AMRIS assistance in purchasing the needed hardware or sequences. For large purchases, approval from the 3 T advisory group will also be needed.
Proposals for Advanced Hardware and Extended Project Development Support
- When an investigator or user group purchases a new coil, installs auxiliary equipment, or develops/implements a new acquisition pulse sequence, the time for full implementation, calibration, and QC testing may be beyond the scope of standard protocol development time. If new hardware, MR protocols or sequences are for general use by the larger user community, users may request that a sufficient scanner time be made available at no charge to them for more complex development projects. If needed in this case, Dr. Rosenberg can assist in project development with his consulting time provided by AMRIS Facility. If hardware and/or commercially available MR protocols or sequences are needed, requests may also be made to fund the needed hardware or sequences with 3 T development funds. A development project proposal must be submitted to the AMRIS Facility (to Dr. Long, Dr. Mareci, and Dr. Rosenberg) for preliminary review of feasibility and time needed. It will then be submitted to the full 3 T advisory committee for discussion and review. The advisory committee meets quarterly, but under extenuating circumstances review may be expedited via electronic discussion and recommendations. A development project pursued internally requires a 2-to-3 page proposal with the following information:
- The specific hardware/protocol/sequence proposed (with relevant references). Also include preliminary data supporting feasibility and information on any partner institutions that will be assisting in a transfer of the proposed hardware/protocol/sequence.
- Documentation of user demand for this functionality and funded research projects that will benefit.
- A proposed development budget detailing instrument development time, staff consulting time, any funds needed for scanner hardware (i.e. coils) or software purchases, and any funds needed for auxiliary (third party) equipment or data analysis software. Attach relevant quotes for hardware and or software packages.
- If approved, the AMRIS Facility will make purchases and allocate the needed development time during off-peak hours of operations (i.e. after 2 pm on weekdays or on weekends). When applying to funding agencies to obtain new equipment or software beyond what can be funded through 3 T development funds, the AMRIS facility can provide a letter of support for the development time needed to implement new protocols utilizing them provided the 3 T advisory committee has approved a development project for them.
- Investigator(s) are also encouraged to review with Dr. Rosenberg their needs for processing and analysis of data acquired on the 3 T MRI/S scanner to ensure sufficient resources are allocated for this purpose in grant applications.