NMR and MRI of blood-dissolved hyperpolarized Xe-129 in different hollow-fiber membranes

Magnetic resonance of hyperpolarized (129)Xe has found a wide field of applications in the analysis of biologically relevant fluids. Recently, it has been shown that the dissolution of hyperpolarized gas into the fluid via hollow-fiber membranes leads to bubble-free (129)Xe augmentation, and thus to an enhanced signal. In addition, hollow-fiber membranes permit a continuous operation mode. Herein, a quantitative magnetic resonance imaging and spectroscopy analysis of a customized hollow-fiber membrane module is presented. Different commercial hollow-fiber membrane types are compared with regard to their (129)Xe dissolution efficiency into porcine blood, its constituents, and other fluids. The presented study gives new insight into the suitability of these hollow-fiber membrane types for hyperpolarized gas dissolution setups.     

Monitoring transport phenomena of paramagnetic metal-ion complexes inside catalyst bodies with magnetic resonance imaging

An indirect magnetic resonance imaging (MRI) method has been developed to determine in a noninvasive manner the distribution of paramagnetic Co2+ complexes inside Co/Al2O3 catalyst extrudates after impregnation with Co2+/citrate solutions of different pH and citrate concentrations. UV/Vis/NIR microspectroscopic measurements were carried out simultaneously to obtain complementary information on the nature of the Co2+ complexes. In this way, it could be confirmed that the actual distribution of Co2+ inside the extrudates could be derived from the MRI images. By combining these space- and time-resolved techniques, information was obtained on both the strength and the mode of interaction between [Co(H2O)6]2+ and different Co2+ citrate complexes with the Al2O(3) support. Complexation of Co2+ by citrate was found to lead to a stronger interaction of Co with the support surface and formation of an eggshell distribution of Co2+ complexes after impregnation. By addition of free citrate and by changing the pH of the impregnation solution, it was possible to obtain the rather uncommon egg-yolk and egg-white distributions of Co2+ inside the extrudates after impregnation. In other words, by carefully altering the chemical composition and pH of the impregnation solution, the macrodistribution of Co2+ complexes inside catalyst extrudates could be fine-tuned from eggshell over egg white and egg yolk to uniform.     

Chemical design of nanoparticle probes for high-performance magnetic resonance imaging

Synthetic magnetic nanoparticles (MNPs) are emerging as versatile probes in biomedical applications, especially in the area of magnetic resonance imaging (MRI). Their size, which is comparable to biological functional units, and their unique magnetic properties allow their utilization as molecular imaging probes. Herein, we present an overview of recent breakthroughs in the development of new synthetic MNP probes with which the sensitive and target-specific observation of biological events at the molecular and cellular levels is possible.     

Quantitative magnetic resonance imaging of urea and lysozyme in protein chromatography

Magnetic resonance imaging (MRI) techniques have been implemented to enable quantitative imaging of protein and urea within a 5 ml HiTrap size-exclusion chromatography desalting column, without introduction of contrast agents. One-, two- and three-dimensional images of urea injected at concentrations of 2, 4, 6 and 8 M were acquired. One-dimensional profiles of lysozyme at concentrations between 5 and 25 mg ml(-1) were also obtained. All data were accurate to within +/- 15% when compared to the known amount injected. Quantitative MRI elution profiles of both urea and lysozyme were then obtained in real-time during a desalting separation.     

Dynamic nuclear polarization studies of nitroxyl spin probes in agarose gel using Overhauser‐enhanced magnetic resonance imaging

Agarose is a tissue‐equivalent material and its imaging characteristics similar to those of real tissues. Hence, the dynamic nuclear polarization studies of 3‐carboxy‐2,2,5,5‐tetramethyl‐pyrrolidine‐1‐oxyl (carboxy‐PROXYL) in agarose gel were carried out. The dynamic nuclear polarization parameters such as spin lattice relaxation time, longitudinal relaxivity, leakage factor, saturation parameter and coupling parameter were estimated for 2 mM carboxy‐PROXYL in phosphate‐buffered saline solution and water/agarose mixture (99 : 1). From these results, the spin probe concentration was optimized as 2 mM, and the reduction in enhancement was observed for carboxy‐PROXYL in water/agarose mixture (99 : 1) compared with phosphate‐buffered saline solution. Phantom imaging was also performed with 2 mM concentration of carboxy‐PROXYL in various concentrations of agarose gel at various radio frequency power levels. The results from the dynamic nuclear polarization measurements agree well with the phantom imaging results. These results pave the way for designing model system for human tissues suited to the biological applications of electron spin resonance/Overhauser‐enhanced magnetic resonance imaging.     

Kinetics from indirectly detected hyperpolarized NMR spectroscopy by using spatially selective coherence transfers

An important recent development in NMR spectroscopy is the advent of ex situ dynamic nuclear polarization (DNP) approaches, which are capable of yielding liquid‐state sensitivities that exceed considerably those afforded by the highest‐field spectrometers. This increase in sensitivity has triggered new research avenues, particularly concerning the in vivo monitoring of metabolism and disease by NMR spectroscopy. So far such gains have mainly materialized for experiments that focus on nonprotonated, low‐γ nuclei; targets favored by relatively long relaxation times T₁, which enable them to withstand the transfer from the cryogenic hyperpolarizer to the reacting centers of interest. Recent studies have also shown that transferring this hyperpolarization to protons by indirectly detected methods could successfully give rise to ¹H NMR spectra of hyperpolarized compounds with a high sensitivity. The present study demonstrates that, when merged with spatially encoded methods, indirectly detected ¹H NMR spectroscopy can also be exploited as time‐resolved hyperpolarized spectroscopy. A methodology is thus introduced that can successfully deliver a series of hyperpolarized ¹H NMR spectra over a minutes‐long timescale. The principles and opportunities presented by this approach are exemplified by following the in vitro phosphorylation of choline by choline kinase, a potential metabolic marker of cancer; and by tracking acetylcholine’s hydrolysis by acetylcholine esterase, an important enzyme partaking in synaptic transmission and neuronal degradation.     

The detection of tetrahydrofuran hydrate formation and saturation using magnetic resonance imaging technique

Tetrahydrofuran (THF) hydrate was formed in bulk as well as in glass beads pack with a mean diameter of 3.0 mm by controlling the temperature under ambient pressure. Images of THF hydrate formation procedure were obtained using the magnetic resonance imaging (MRI) technique. The experiment results showed that MRI is an effective method for the detection of hydrate formation. Saturation of hydrate formed both in bulk and glass beads can be confirmed by intensity integration of MRI images.     

A comparison of magnetic resonance imaging methods for fluid content imaging in porous media

Quantitative measurements are important for imaging fluid content in porous media. Conventional MRI methods suffer from contrast because of relaxation times in porous media, resulting in measurements of apparent fluid content, not the true fluid content. We compare four magnetic resonance imaging methods for fluid content imaging in several water‐saturated reservoir core plugs: frequency‐encoded spin echo, single point ramped imaging with T₁ enhancement, hybrid spin echo single point imaging (SE‐SPI), and T₂ mapping SE‐SPI. 1‐D profiles obtained with each method were compared in terms of image quality, image sensitivity, and quantification of water content. The image quality of short T₂ lifetime samples suffered from blurring in hybrid SE‐SPI images. Image sensitivity was the highest in the profiles obtained with frequency‐encoded spin echo. The quantification of frequency‐encoded spin echo, T₂ mapping SE‐SPI, and hybrid SE‐SPI suffered in core plugs with a significant population of short T₂ components because of T₂ attenuation. Overall, single point ramped imaging with T₁ enhancement was found to be the most general method for fluid content imaging. Copyright © 2013 John Wiley & Sons, Ltd.     

Synthesis,Solid‐State NMR Characterization,and Application for Hydrogenation Reactions of a Novel Wilkinson’s‐Type Immobilized Catalyst

Silica nanoparticles (SiNPs) were chosen as a solid support material for the immobilization of a new Wilkinson’s‐type catalyst. In a first step, polymer molecules (poly(triphenylphosphine)ethylene (PTPPE); 4‐diphenylphosphine styrene as monomer) were grafted onto the silica nanoparticles by surface‐initiated photoinferter‐mediated polymerization (SI‐PIMP). The catalyst was then created by binding rhodium (Rh) to the polymer side chains, with RhCl₃ ? x H₂O as a precursor. The triphenylphosphine units and rhodium as Rh^I provide an environment to form Wilkinson’s catalyst‐like structures. Employing multinuclear (³¹P, ²⁹Si, and ¹³C) solid‐state NMR spectroscopy (SSNMR), the structure of the catalyst bound to the polymer and the intermediates of the grafting reaction have been characterized. Finally, first applications of this catalyst in hydrogenation reactions employing para‐enriched hydrogen gas (PHIP experiments) and an assessment of its leaching properties are presented.