arXiv subjects

Josh P. Peters

Publications and source records attributed to Josh P. Peters.

3 recordsLinked to original sources

arXiv2025

Over four minutes relaxation of pyruvate using chemically and physically induced deceleration of relaxation

[1-13C]pyruvate is the most widely used tracer for hyperpolarized metabolic magnetic resonance imaging, with profound applications in tumor and inflammation diagnosis as well as treatment monitoring. The most fundamental hurdle to broader application, however, remains the rapid polarization relaxation and the associated signal loss. Here, we report a method to address this challenge. Studying the nuclear spin relaxation dispersion of [1-13C]pyruvate across magnetic fields from 8 μT to 9.4 T, as a function of additives, solvents, and preparation methods, allowed us to achieve relaxation times of up to four minutes. Such a long time could enable reliable quality control and nearly polarization loss-free transport, further boosting the power of hyperpolarized metabolic MRI.

physics.chem-ph↗

arXiv2025

Compact magnetic field cycling system with the range from nT to 9.4 T exemplified with 13C relaxation dispersion and SABRE-SHEATH hyperpolarization

We present a compact magnetic field cycling system for high-resolution NMR spectrometers. The system enables the transfer of the sample from B0 field of 9.4 T to about nT and all fields in between within 1 second. Utilizing a flexible gear rod made the shuttling system more compact, reducing the height to about the height required for filling liquid helium - hence, it can be installed in average-size NMR laboratories (the height of NMR with MFC is only 3.32 m). The system utility is exemplified by measuring T1 relaxation dispersion of the most common liquid state hyperpolarization tracer - [1-13C]pyruvate - and magnetic field dependences of signal amplification by reversible exchange enabling alignment transfer to heteronuclei (SABRE-SHEATH) hyperpolarization of [15N]pyridine. Using the system, we uncovered the exact relaxation of the pyruvate for a common preclinical dDNP sample composition and gave quantitative estimates for the retained polarization after sample transfer. We modified the observation protocol of SABRE-SHEATH polarization, which, with the high reproducibility of the MFC, provided us with a method to measure the chemical exchange rates of hyperpolarized compounds.

physics.chem-ph↗

arXiv2025

Maximizing NMR Sensitivity: A Guide to Receiver Gain Adjustment

Novel methods and technology drive the rapid advances of nuclear magnetic resonance (NMR). The primary objective of developing novel hardware is to improve sensitivity and reliability (and possibly to reduce cost). Automation has made NMR much more convenient, but it may lead to trusting the algorithms without regular checks. In this contribution, we analyzed the signal and signal-to-noise ratio (SNR) as a function of the receiver gain (RG) for 1H, 2H, 13C, and 15N nuclei on five spectrometers. On a 1 T benchtop spectrometer (Spinsolve, Magritek), the SNR showed the expected increase as a function of RG. Still, the 1H and 13C signal amplitudes deviated by up to 50% from supposedly RG-independent signal intensities. On 7, 9.4, 11.7, and 14.1 T spectrometers (Avance Neo, Bruker), the signal intensity increases linearly with RG as expected, but surprisingly a drastic drop of SNR is observed for some X-nuclei and fields. For example, while RG = 18 provided a 13C SNR similar to that at a maximum RG of 101 at 9.4 T, at RG = 20.2 the determined SNR was 32% lower. The SNR figures are strongly system and resonance frequency dependent. Our findings suggest that NMR users should test the specific spectrometer behavior to obtain optimum SNR for their experiments, as automatic RG adjustment does not account for the observed characteristics. In addition, we provide a method to estimate optimal settings for thermally and hyperpolarized samples of a chosen concentration, polarization, and flip angle, which provide a high SNR and avoid ADC-overflow artefacts.

physics.ins-det↗