{"paper_id":"ec4ff71d-94c5-4840-a125-ab684ad075ab","body_text":"The device and US protocols were evaluated with tissue‐mimicking, agar‐based phantoms. No animals or patient data were included in this study. Therefore, no informed consent from patients or approval from an Ethics Committee was required.\nThe device includes two computer‐controlled axes (z and y on MRI). Figure  1  shows a drawing of the linear axis for motion along the MRI y‐axis. The y‐plate was coupled to a threaded plastic screw, which was attached to the shaft of a piezoelectric motor (USR 30‐S3; Shinsei Kogyo Corp, Tokyo, Japan). The rotation of this shaft converts the angular motion to linear. An optical encoder module (US Digital Corporation, Vancouver, WA) was attached under the y‐axis frame to record the motion of the encoder strip. The encoder module (EM1‐0‐500‐I; US Digital Corporation) was used for both stages. The encoder output is wired to the counter pin of a data acquisition board (6251; National instruments, Austin, TX). Figure  2  shows the position of the transmissive optical encoder module for controlling linear motion. A photograph of the finalized y‐stage motion component is shown in Figure  3 .\nComputer‐aided design drawing of the linear axis for motion along the MRI y‐axis.\nPlacement of the encoder modules in one of the linear stages.\nDeveloped y‐axis stage.\nCompared to our previous small‐animal positioning device, \n 22 \n  the main difference is the size of the motor, which is smaller in the current device (almost 50% smaller). This enabled us to design a smaller positioning device. The z‐axis stage was coupled to the y‐axis with a simple structure, as shown in Figure  4 . The principle of movement of the z‐stage and its range were the same as for the y‐stage. The placement of the encoder followed the same technique as the y‐stage. The transducer arm was coupled to the z‐axis plate, as shown in Figure  4 . Acoustic coupling was established by immersing the transducer in a tank with degassed water.\nCoupling of the two linear stages (z‐axis stage and y‐axis stage). The transducer arm was coupled to the z‐axis plate.\nA 3‐dimensional computer‐aided model of the positioning device was designed in MicroStation version 8 (Bentley Systems, Inc, Exton, PA), which was later fabricated in acrylonitrile butadiene styrene material by using fusion deposition modeling technology (FDM400; Stratasys, Eden Prairie, MN).\nThe positioning device can be placed on the table of any commercial MRI scanner except a 9.4‐T scanner. The dimensions of the device with all axes extended do not exceed greater than 7, 40, and 15 cm in height, length, and width, respectively. The motion range of the robot is 6 for both axes. The positioning device weighs around 2.3 kg. Figure  5  shows the interior of the device, and Figure  6  shows the entire device.\nInterior of the positioning device.\nComplete robotic system showing both linear axes.\nTo prevent motion of the mouse, a specially designed holder was developed. When the mouse is positioned in the supine position, sideways movable holders are pushed toward the mouse, preventing any mouse movement (Figure  7 ). Figure  8  shows a mouse placed in the experimental setting.\nComputer‐aided design drawing of the mouse holder.\nMouse holder.\nAn application was developed using the C# programming language (Visual Studio 2010 Express; Microsoft Corporation, Redmond, WA), which aimed to enhance the user interface. The two motion axes of the device are controlled by selecting an automated algorithm \n 23 \n  or by specifying a direction and step to move. The software includes additional functions, such as an interface with the MRI, magnetic resonance (MR) thermometry, and US control (eg, frequency, power, and sonication time).\nThe metallic housing containing the positioning device's motor drivers was kept outside the Faraday cage to eliminate the possibility of electromagnetic interference. Each US motor is driven by its corresponding driver (D6030; Shinsei Kogyo Corp). The drivers are powered with 24 V, which is provided by a DC power supply. A universal serial bus data acquisition board (6251; National Instruments) was wired to the drivers to rotate the motors in a clockwise or anticlockwise direction based on instructions from the software.\nThe high‐intensity focused US system includes a signal generator (HP 33120A; Agilent Technologies, Englewood, CO), a radiofrequency amplifier (AG1012; T & C Power Conversion, Inc, Rochester, NY), and a 50‐mm‐diameter spherical transducer (Medsonic Ltd, Limassol, Cyprus) operating at 0.5 MHz with an 80‐mm focal length. The transducer consists of a type P762 piezoceramic active element (Ferroperm; Kvistgaards, Denmark) sealed with a thermoresistant epoxy backing material for damping excessive vibrations. The impedance of the transducer was matched to 50 Ω. The transmission of high‐frequency harmonics was reduced by connecting a custom‐made low‐pass filter with a cutoff frequency of 10 MHz in series.\nThe performance of the high‐intensity FUS transducer was assessed through a series of sonications using a tissue‐mimicking, agar‐based phantom. The phantom was fabricated by following a recipe that was developed and characterized previously for its properties by our group. \n 24 \n ,  \n 25 \n  Magnetic resonance thermometry was used to monitor the temperature–time profile and deposition of heat in the phantom during sonications. The efficacy of the exposure protocols was assessed by using the produced color‐coded thermal maps.\nThe system was evaluated in one New Zealand rabbit that was transferred to the laboratory from an approved farm.\nThe positioning device system was tested in a 1.5‐T MR system (Signa 1.5 T; GE Healthcare, Fairfield, CT). Magnetic resonance imaging with a high resolution was conducted to visualize the phantom/transducer setup. A T2‐weighted fast spin echo sequence was used with the following parameters: repetition time, 2500 milliseconds; echo time, 60 milliseconds; slice thickness, 3 mm; matrix, 256 × 256; field of view, 16 cm; number of excitations, 3; and echo train length, 8. A T1‐weighted spoiled gradient sequence was used for acquiring MR thermometry: repetition time, 50 milliseconds; echo time, 2.7 milliseconds; field of view, 16 cm; matrix, 256 × 256; flip angle, 30°; and number of excitations, 1.\nThe temperature during the high‐intensity focused US protocol was estimated by the proton resonance frequency shift equation reported first by Ishihara et al. \n 26 \n  The equation corelates the temperature elevation (Δ T ) with the measured phase as follows: ΔT = φ T − φ T 0 γα Β 0 TΕ , where  φ ( T ) and  φ ( T \n 0 ) are the phases at an initial temperature ( T ) and at a final temperature ( T \n 0 );  α  is the pulse repetition frequency change coefficient;  γ  is the gyromagnetic ratio;  B \n 0  is the magnetic field strength; and  TE  is the echo time. The spoiled gradient pulse sequence was used to acquire the MRI thermometric maps.\n\nThe accuracy of the linear axis (y) was assessed comparing the intended step to the actual distance that the robot was moved. Figure  9  shows the difference of the measured distance to the intended distance. This procedure was repeated for step sizes of 1 to 10 mm. The values on the vertical axis represent the measured distance, which for each step was calculated by the average of 20 such measurements. The measured distance was 0.04 mm larger compared to the intended distance for a 1‐mm step, whereas for a 10‐mm step, the difference was 0.1 mm larger compared to the intended step. Similar differences were observed for the z‐axis. The smallest step that could be achieved in any linear axis was 0.1 mm.\nMeasured linear step versus intended step in millimeters for the y‐axis.\nThe next series of figures were obtained in the MRI setting. Figure  10  shows a T2‐weighted fast spin echo MR image of the transducer of the positioning device and the agar phantom that was used to produce MR thermometry. No MRI compatibility evaluation was performed, since the same motors and encoders were used in previous studies by our group. \n 23 \n ,  \n 27 \n ,  \n 28 \n ,  \n 29 \n  Note the excellent contrast between water, the agar‐based phantom, and the transducer. The images did not reveal any air spaces between the water and agar phantom interface. The image coil was placed around the agar‐based phantom.\nT2‐weighted fast spin echo MRI of the transducer of the positioning device and the agar phantom that was used to produce MR thermometry.\nA time series of MR thermometry in the coronal plane with a 12‐second temporal resolution used to monitor heat deposition in the phantom induced by a 20‐W, 60‐second sonication is shown in Figure  11 . Figure  12  shows the corresponding MR thermometric time series in the sagittal plane, showing heat build‐up induced by the proposed transducer.\nMagnetic resonance thermometric map in a coronal plane at different intervals (every 12 seconds) using acoustic power of 20 W for 60 seconds.\nMagnetic resonance thermometric map in a sagittal plane at different intervals (every 12 seconds) using acoustic power of 20 W for 60 seconds.\nFigure  13  shows an MR thermometric map in a coronal plane, showing the motion of one of the linear stages of the positioning devices. Heating was induced at each step via 20‐W acoustic power sonications applied for 20 seconds. The intended spatial step was 10 mm. The average distance measured by MR thermometry was 9.95 mm with an SD of 0.2 mm (n = 12).\nMagnetic resonance thermometric map in a coronal plane showing the motion of one of the linear stages of the positioning devices. The acoustic power used was 20 W for 60 seconds.\nFigure  14  shows a temperature map produced in the thigh muscle of a rabbit. The power used was 27 W for 60 seconds. The temperature map is in a plane parallel to the transducer propagation. Despite the small dimensions of the thigh, it was possible to place the beam in the center of the thigh muscle.\nTemperature map produced in the thigh muscle of a rabbit. The power used was 27 W for 60 seconds. The temperature map is in a plane parallel to the transducer propagation.\n\nAn MRgFUS positioning device was developed for use with small animals (mice, rats, and rabbits), which can fit in commercial MRI scanners up to 7 T with a bore diameter of 30 cm or larger. The motion accuracy of the positioning device was tested with MR thermometry by using 10‐mm steps. The measured distance was compared to the intended distance, resulting in excellent spatial accuracy. The tests were performed in a custom‐made agar/silica/evaporated milk gel phantom.\nThe positioning device can displace the transducer in the z‐ and y‐axes with adequate accuracy; therefore, a predefined grid of thermal lesions can be delivered. The system has the ability to image and move at the same time because of the use of piezoelectric motors and optical encoders that are MRI compatible.\nThe proposed system displays a 6‐cm range of motion in both axes, which offers sufficient coverage for most applications. The design of this robot can be scaled up so that it can be applied in humans. It can be extended to greater than 15 cm in both axes and therefore can be used for 1.5‐ or 3‐T MRI scanners. The positioning device is 7 cm in height. With an improved design, this can be reduced even further. With the above‐mentioned adjustments to the design, the proposed system can enter the market for human use in the abdominal area (liver, kidney, and pancreas), fibroids, or the breast. The expansion to a human positioning device will require the addition of one computer‐controlled linear axis and two computer‐controlled angular axes.\nThe MR thermometry shown in Figures  10  and  11  demonstrated the heating capabilities of the low‐frequency transducer by using the pulse repetition frequency method. This type of transducer is suitable for transcranial sonication of mice. \n 30 \n  A thorough evaluation of the transducer's heating performance in small‐animal models is essential.\nThe accuracy of the linear‐displacement axis was not compromised in the vicinity of the MRI‐compatible encoders and was equal to 0.1 mm, which exceeded the requirements of interventional oncology applications. It is the group's target to expand the portfolio by designing and producing MRI‐compatible positioning devices specific to new FUS surgical applications. As mentioned elsewhere, the goal is to add additional axes (one linear and two angular) to use it in the clinical setting with improved maneuverability. The key advantages of the proposed positioning device are the low cost and simplicity, but it is functional and accurate device.\nThe main innovation of this device is that its size is small compared to other available devices. The compactness of the system improves handling of the anesthetized animal by leaving more free space for the associated accessories and immobilization pads. Additionally, the device can fit in MRI systems with bore sizes as small as 30 cm. Currently, the only device that can do this \n 20 \n  uses phased arrays, which steer the beam electronically. To our knowledge, there is another single‐element transducer system for small animals \n 31 \n  but with a completely different design. The design of the system is simpler yet as effective as phased arrays, and the production cost is affordable, since sonications are performed via a monoelement focused transducer. In our opinion, for experimental work in small animals, the use of a positioning device with two axes and the use of a single‐element transducer are sufficient.","source_license":"CC-BY-4.0","license_restricted":false}