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Praveen Iyyappan Valsala

Publications and source records attributed to Praveen Iyyappan Valsala.

2 recordsLinked to original sources

Overcoming the limitations of NMR Field Probes: A Novel Integrated Sensor Utilizing Pre-Polarization for (Ultra) Low Field MRI

Access to magnetic resonance imaging (MRI) remains severely limited in low- and middle-income countries, especially in sub-Saharan Africa, despite rising rates of non-communicable diseases. Low-field MRI presents an affordable, locally developable diagnostic solution, but its performance is constrained by magnetic field instability. We present a novel NMR field probe designed to overcome these challenges using a rapid non-adiabatic switch-off of a pre-polarization field resulting in precessing spin magnetization. Achieved by first use of high-voltage silicon carbide transistors operating in controlled avalanche breakdown, it measures the Larmor frequency without prior field knowledge, unlike conventional probes. This capability is crucial during magnet development with often unknown fields, allowing early detection of magnet issues, and offering an urgently needed tool for magnet design and image-quality improvement. Validated from 1 mT to 45 mT (up to 1,000 times stronger than similar systems) its low-cost, modular design supports replication, upgrades, and enhanced field control, helping expand global MRI access.

physics.med-ph↗

High-resolution deuterium metabolic imaging of the human brain at 9.4 T using bSSFP spectral-spatial acquisitions

We demonstrated the feasibility of using bSSFP acquisitions for off-resonance insensitive high-resolution [6,6'-2H2]-glucose deuterium metabolic imaging (DMI) studies in the healthy human brain at 9.4T. Balanced SSFP acquisitions have potential to improve the sensitivity of DMI despite the SNR loss of phase-cycling and other human scanner constraints.We investigated two variants of bSSFP acquisitions, namely uniform-weighted multi echo and acquisition-weighted CSI to improve the SNR of deuterium metabolic imaging (DMI) in the brain with oral labelled-glucose intake. Phase-cycling was introduced to make bSSFP acquisitions less sensitive to B0 inhomogeneity. Two SNR optimal methods for obtaining metabolite amplitudes from the phase-cycled data were proposed. The SNR performance of the two bSSFP variants was compared with a standard gradient-spoiled CSI acquisition and subsequent IDEAL processing. In addition, in vivo T1 and T2 of water, glucose and Glx (glutamate+glutamine) were estimated from non-localized inversion recovery and spin-echo measurements.High-resolution whole-brain dynamic quantitative DMI maps were successfully obtained for all three acquisitions. Phase-cycling improved the quality of bSSFP metabolite estimation and provided additional spectral encoding. The SNR improvement was only observed for the CSI variant of bSSFP acquisitions with an average increase of 18% and 27% for glucose and Glx, respectively, compared to the vendor's CSI. ME-bSSFP acquisition achieved higher resolutions than acquisition-weighted CSI and exhibited several qualitative improvements.

physics.med-ph↗