Three-dimensional Oximetric Electron Paramagnetic Resonance Imaging using the Single Point Imaging modality generates unpaired spin density and oxygen images that can readily distinguish between normal and tumor tissues in small animals. It is also possible with fast imaging to track the changes in tissue oxygenation in response to the oxygen content in the breathing air. However, this involves dealing with gigabytes of data for each 3D oximetric imaging experiment involving digital band pass filtering and background noise subtraction, followed by 3D Fourier reconstruction. This process is rather slow in a conventional uniprocessor system. This paper presents a parallelization framework using OpenMP runtime support and parallel MATLAB to execute such computationally intensive programs. The Intel compiler is used to develop a parallel C++ code based on OpenMP. The code is executed on four Dual-Core AMD Opteron shared memory processors, to reduce the computational burden of the filtration task significantly. The results show that the parallel code for filtration has achieved a speed up factor of 46.66 as against the equivalent serial MATLAB code. In addition, a parallel MATLAB code has been developed to perform 3D Fourier reconstruction. Speedup factors of 4.57 and 4.25 have been achieved during the reconstruction process and oximetry computation, for a data set with 23 x 23 x 23 gradient steps. The execution time has been computed for both the serial and parallel implementations using different dimensions of the data and presented for comparison. The reported system has been designed to be easily accessible even from low-cost personal computers through local internet (NIHnet). The experimental results demonstrate that the parallel computing provides a source of high computational power to obtain biophysical parameters from 3D EPR oximetric imaging, almost in real-time.
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http://dx.doi.org/10.1155/2009/528639 | DOI Listing |
PLoS One
July 2024
Department of Pediatrics and Adolescent Medicine, Division of Neonatology, Comprehensive Center for Pediatrics, Pediatric Intensive Care & Neuropediatrics, Medical University of Vienna, Vienna, Austria.
Objective: To determine the effect of different types of probes for lung ultrasound in neonates.
Design: Prospective, blinded, randomized, comparative study between 2020 and 2022.
Setting: Single-center study at a third level neonatal unit.
Mol Imaging Biol
June 2024
In Vivo Multifunctional Magnetic Resonance Center at Robert C. Byrd Health Sciences Center, West Virginia University, Morgantown, WV, USA.
Purpose: Bioprinting is an additive manufacturing technology analogous to 3D printing. Instead of plastic or resin, cell-laden hydrogels are used to produce a construct of the intended biological structure. Over time, cells transform this construct into a functioning tissue or organ.
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June 2024
Department of Pharmaceutical Sciences, School of Pharmacy, West Virginia University, Morgantown, WV, 26506, USA.
Purpose: This study aimed to develop a biocompatible oximetric electron paramagnetic resonance (EPR) spin probe with reduced self-relaxation, and sensitivity to oxygen for a higher signal-to-noise ratio and longer relaxation times at high oxygen concentration, compared to the reference spin probe OX071.
Procedures: SOX71 was synthesized by succinylation of the twelve alcohol groups of OX071 spin probe and characterized by EPR at X-Band (9.5 GHz) and at low field (720 MHz).
Magn Reson Med
January 2024
Radiation Biology Branch, Center for Cancer Research, NCI, Bethesda, Maryland, USA.
Purpose: In this study, we compared two triarylmethyl (TAM) spin probes, Ox071 and Ox063 for their efficacy in measuring tissue oxygen levels under hypoxic and normoxic conditions by R *-based EPR oximetry.
Methods: The R * dependencies on the spin probe concentration and oxygen level were calibrated using deoxygenated 1, 2, 5, and 10 mM standard solutions and 2 mM solutions saturated at 0%, 2%, 5%, 10%, and 21% of oxygen. For the hypoxic model, in vivo imaging of a MIA PaCa-2 tumor implanted in the hind leg of a mouse was performed on successive days by R *-based EPR oximetry using either Ox071 or Ox063.
Magn Reson Med
September 2022
Laboratory for Structural Physiologic and Functional Imaging, Department of Radiology, University of Pennsylvania, Philadelphia, PA, USA.
Purpose: Cerebral metabolic rate of oxygen (CMRO ) is an important biomarker of brain function. Key physiological parameters required to quantify CMRO include blood flow rate in the feeding arteries and venous oxygen saturation (SvO ) in the draining vein. Here, a pulse sequence, metabolism of oxygen via T and interleaved velocity encoding (MOTIVE), was developed to measure both parameters simultaneously and enable CMRO quantification in a single pass.
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