<p>The work in this thesis deals with pre-clinical development of rapid in vivo <sup>31</sup>P mag- netic resonance spectroscopy (MRS) techniques. Current MRI literature of <sup>31</sup>P spec- troscopy presents evidence of increased concentrations of phosphomonoesters (PME), and phosphodiester (PDE) as well as inorganic phosphate concentrations in tumor tissue. Human breast cancer studies have demonstrated correlation between disease progression and both PME and PDE peaks. Furthermore, <sup>31</sup>P MRS can be used to detect, grade tumours and monitor response to chemo and radiation therapy.<br />Tumor measurements are typically static (i.e. single measurement per scan). In other experiments, on muscle for example, dynamic measures are required the purpose of which is to assess temporal function and recovery. In all <sup>31</sup>P acquisitions there are problems surrounding RF coil design, pulse sequence speed, localization and system calibration. The work presented here focused on improving all these aspects and provide easy and reliable work flow to use <sup>31</sup>P MRS in a clinical setting.<br />One of the aspects of this thesis lies in designing and construction of an RF coil that is well suited for integration with a clinical MRI breast imaging and biopsy system. The designed coil was tuned for simultaneous operation at <sup>31</sup>P (51.73 MHz) and <sup>1</sup>H (127.88MHz) Larmor frequencies. This design has advantages in the fact that complex pulse sequences with heteronuclear decoupling could be performed easily. The additional features of the coil design is that it is possible to swap it into the breast imaging system without moving the patient. Along with the designed coil, custom software was written to assist with transmit gain calibration of <sup>31</sup>P RF pulses, to ensure maximum MR signal. The automated prescan ensures easy work flow and minimizes the operator variability and patient time inside the MR scanner.<br />Another aspect of this thesis deals with rapid pulse sequence development, to further speed up the <sup>31</sup>P MRS data acquisition. Echo planar spectroscopic imaging (EPSI) with a fly–back gradient trajectory is currently one of the most reliable and robust techniques for speeding up chemical shift imaging (CSI) acquisitions. A <sup>31</sup>P EPSI sequence was written to acquire spectroscopic imaging data at 1, 2 and 2.6 cm spatial resolution and spectral bandwidth of 3125 Hz. The sequence showed an ability to speed up data acquisition up to 16 times, where SNR permits.<br />Phantom studies were used to verify the double tuned coil and EPSI sequence en- suring proper and safe operation. In vivo measurements of an exercising muscle demonstrated the ability of <sup>31</sup>P EPSI to play an important role in rapidly acquiring spatially localized <sup>31</sup>P spectroscopic data.<br />With these preclinical developments in place a clinical trial is possible using <sup>31</sup>P MRS rapidly and efficiently. Furthermore the increased usability of <sup>31</sup>P MRS provided by the tools developed in this thesis can prove to be beneficial by integrating <sup>31</sup>P MRS into existing clinical protocols.</p> / Doctor of Science (PhD)
| Identifer | oai:union.ndltd.org:mcmaster.ca/oai:macsphere.mcmaster.ca:11375/8956 |
| Date | 10 1900 |
| Creators | Obruchkov, Sergei I. |
| Contributors | Michael D. Noseworthy, Ph.D, Alex Bain, Ph.D, Charles Cunningham, Ph.D and Michael Patterson, Ph.D, Medical Physics |
| Source Sets | McMaster University |
| Detected Language | English |
| Type | thesis |
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