Trehalose as an alternative to glycerol as a glassing agent for in vivo DNP MRI. Issue 1 (22nd July 2020)

• Record Type: Journal Article
• Authors: Brender, Jeffrey R.; Kishimoto, Shun; Eaton, Gareth R.; Eaton, Sandra S.; Saida, Yu; Mitchell, James; Krishna, Murali C.
• Is Part Of: Magnetic resonance in medicine. Volume 85:Issue 1(2021)
• Page Start: 42
• Page End: 48
• Publication Date: 2020-07-22
• Subjects: dynamic nuclear polarization -- glassing -- OX063 -- EPR -- relaxation; Nuclear magnetic resonance -- Periodicals; Electron paramagnetic resonance -- Periodicals; 616.07548
• DOI: 10.1002/mrm.28405
• Languages: English
• ISSNs: 0740-3194

Abstract

Abstract : Purpose: In dynamic nuclear polarization (DNP), the solution needs to form a glass to attain significant levels of polarization in reasonable time periods. Molecules that do not form glasses by themselves are often mixed with glass forming excipients. Although glassing agents are often essential in DNP studies, they have the potential to perturb the metabolic measurements that are being studied. Glycerol, the glassing agent of choice for in vivo DNP studies, is effective in reducing ice crystal formation during freezing, but is rapidly metabolized, potentially altering the redox and adenosine triphosphate balance of the system. Methods: DNP buildup curves of 13 C urea and alanine with OX063 in the presence of trehalose, glycerol, and other polyol excipients were measured as a function of concentration. T1 and Tm relaxation times for OX063 in the presence of trehalose were measured by EPR. Results: Approximately 15–20 wt% trehalose gives a glass that polarizes samples more rapidly than the commonly used 60%‐wt formulation of glycerol and yields similar polarization levels within clinically relevant timeframes. Conclusions: Trehalose may be an attractive biologically inert alternative to glycerol for situations where there may be concerns about glycerol's glucogenic potential and possible alteration of the adenosine triphosphate/adenosine diphosphate and redox balance.