Biomedical subjects

Paul T Callaghan

Publications and source records attributed to Paul T Callaghan.

11 recordsLinked to original sources

PubMed2006

Imaged deconvolution: a method for extracting high-resolution NMR spectra from inhomogeneous fields.

We present a novel method for obtaining high resolution NMR spectra in the presence of grossly inhomogeneous magnetic fields, such as those encountered in one-sided access NMR. Our method combines the well-known principle of reference deconvolution with NMR imaging in order to resolve spectral features with frequency resolution orders of magnitude smaller than the prevailing line-broadening due to field inhomogeneity. We demonstrate that, in cases of inhomogeneous field line-broadening more than an order of magnitude larger than the spectral features to be resolved, rather than performing reference deconvolution on the sample as a whole, it is more favourable in terms of SNR to divide the target region of a sample into smaller sub-regions, by means of chemical shift imaging, and then to perform reference deconvolution on the individual sub-region spectra, finally summing the results In this way, significant resolution enhancements can be obtained in the presence of severe magnetic field inhomogeneity without an unacceptable loss in SNR.

Algorithms↗

PubMed2006

Evolution of a lamellar domain structure for an equilibrating lyotropic liquid crystal.

Aerosol OT/water exhibits a lamellar phase over a wide range of concentrations. We show, by magnetic resonance (NMR) and scanning electron microscopy (SEM), that the morphology of the lamellar phase varies significantly across that range and that the rate of equilibration depends strongly on concentration (25, 33, and 50 wt %) with, paradoxically, the faster equilibration at higher surfactant concentrations. We find that the 25 wt % sample exhibits a defect-rich local structure, characteristic of a superposed L(3) character. Further into the lamellar region, at 33 wt %, this defect-rich structure persists heterogeneously, while, at 50 wt %, the lamellar phase domains are highly ordered. The NMR methods used here included (2)H spectroscopy and the two-dimensional NMR method, diffusion-diffusion exchange spectroscopy (DEXSY). The latter was used to obtain quantitative information on the domain sizes and defects within the polydomain lamellar mesophase. Comparison of the NMR with the SEM results suggests that, at 25 wt % AOT, bilayer defects play an important role in influencing the (2)H NMR and DEXSY NMR results.

Journal Article↗

PubMed2006

Two-dimensional NMR spectroscopy in Earth's magnetic field.

We demonstrate the first two-dimensional correlation NMR (COSY) spectra obtained at ultra low frequencies (ULF) using the Earth's magnetic field. Using a specially developed spectrometer with multiple audio-frequency pulses under controlled pulse phase, we observe magnetisation transfer arising from heteronuclear J-couplings in trifluoroethanol and para-difluorobenzene. The 2D COSY spectra exhibit all diagonal and off-diagonal multiplets consistent with known J-couplings in these molecules.

Journal Article↗

PubMed2006

A practical and flexible implementation of 3D MRI in the Earth's magnetic field.

The Earth's magnetic field, though weak, is appealing for NMR applications because it is highly homogeneous, globally available and free. However, the practicality of Earth's field NMR (EFNMR) has long been limited by the need to perform experiments in outdoor locations where the local field homogeneity is not disrupted by ferrous or magnetic objects and where ultra-low frequency (ULF) noise sources are at a minimum. Herein we present a flexible and practical implementation of MRI in the Earth's magnetic field that demonstrates that EFNMR is not as difficult as it was previously thought to be. In this implementation, pre-polarization and ULF noise shielding, achieved using a crude electromagnet, are used to significantly improve signal-to-noise ratio (SNR) even in relatively noisy environments. A three axis gradient coil set, in addition to providing imaging gradients, is used to provide first-order shims such that sub-hertz linewidths can routinely be achieved, even in locations of significant local field inhomogeneity such as indoor scientific laboratories. Temporal fluctuations in the magnitude of the Earth's magnetic field are measured and a regime found within which these variations in Larmor frequency produce no observable artefacts in reconstructed images.

Journal Article↗

PubMed2006

Fast magnetic resonance imaging and velocimetry for liquids under high flow rates.

We here demonstrate the use of NMR velocity imaging techniques to measure flow in a free falling jet of water at speeds up to and on the order of 1m/s. In particular, we show how to adapt the RARE imaging method, based on a CPMG multiple rf pulse train, so that the real and imaginary parts of the signal may be suitably acquired, enabling pulsed gradient spin echo encoding for flow. We term this method "soft-pulse-quadrature-cycled PGSE-RARE" or SPQC-PGSE-RARE. We further demonstrate the use of a one-dimensional (slice selective) imaging method which takes advantage of the cylindrical symmetry of the flow, and considerably shortens the image acquisition time.

Journal Article↗

PubMed2006

Orientational anisotropy in the polydomain lamellar phase of a lyotropic liquid crystal.

Diffusion-diffusion correlation measurements by NMR are used to investigate the degree of orientational order in the lamellar phase of Aerosol OT (bis(2-ethylhexyl) sodium sulfosuccinate) and water at a range of surfactant concentrations (25, 33, and 50 wt %). We show that true isotropy of the domains is found at the lowest concentration but that at higher concentrations deviations from isotropy can be found, as evidenced by asymmetry on the 2D correlation distributions. We further discuss the significance of asymmetry in diffusion-diffusion exchange experiments, 2D distributions that should always be symmetric in steady state.

Journal Article↗

PubMed2005

A study of anisotropic water self-diffusion and defects in the lamellar mesophase.

The correlation of molecular diffusion coefficients obtained via a novel two-dimensional pulsed gradient spin-echo (PGSE) NMR method has been shown to reveal detailed structural information on the mesophases of lyotropic liquid crystals. A four-component system containing both nonionic (pentaethylene glycol monododecyl ether) and ionic (sodium dodecyl sulfate) surfactants, water, and decane was prepared and left to equilibrate. In the temperature region around 309 K, a lamellar mesophase forms. A two-dimensional Laplace inverse transformation was performed on the (gammadeltag)2(delta - delta/3) domain data to separate any multiexponential behavior that resulted from local anisotropy. The results of the double PGSE experiment with contiguous gradient pulse pairs, applied both collinearly and orthogonally, clearly show the presence of local anisotropic self-diffusion of the water molecules and suggest a preferred orientation of the lamellae. Information about defects/domain size was obtained by the insertion of a mixing time (t(m)') between the successive gradient pulse pairs. This work highlights the value of this new NMR correlation method in the study of surfactant systems.

Journal Article↗

PubMed2005

Diffusion, relaxation, and chemical exchange in casein gels: a nuclear magnetic resonance study.

Water in protein/water mixtures can be described in terms of bound water and free water, by exchange between these two states, and by its exchange with appropriate sites on the protein. 1H-NMR diffusion and relaxation measurements provide insights into the mobility of these states. T2 relaxation-time dispersions (i.e., T2 relaxation times at different echo pulse spacings) reveal additional information about exchange. We present a comprehensive set of diffusion and T2 dispersion measurements on casein gels for which the protein/water ratio ranges from 0.25 to 0.5. The combination of these methods, taken in conjunction with concentration dependence, allows a good estimate of the parameters required to fit the data with Luz/Meiboom and Carver/Richards models for relaxation and chemical exchange. We compare the exchange (a) between water and protein and (b) between free water and bound water. Further, we attempt to distinguish chemical site exchange and diffusion/susceptibility exchange.

Journal Article↗

PubMed2005

Some perspectives on dispersion and the use of ensemble-averaged PGSE NMR.

Magnetic resonance methodology has made a significant impact in helping us understand the physics of porous media. Among an important class of experiments is that set of techniques designed to measure fluid dispersion. This paper provides some background on some of the underlying physics of dispersion, and outlines some of the NMR approaches that have proven successful. The local and nonlocal dispersion tensors are described and the prospects for future NMR advances considered.

Magnetic Resonance Spectroscopy↗

PubMed2004

Nanoscale NMR velocimetry by means of slowly diffusing tracer particles.

The resolution of NMR velocimetry is inherently limited by random displacements due to molecular self-diffusion, and has so far not extended below a few tens of microns. We report here an extension to the nanoscale domain, a result achieved by the use of slowly diffusing, NMR-visible core-shell latex particles. These particles comprise an oil core surrounded by a solid polymer shell, making spheres of diameter 370 nm. Using these particles in the annulus of a concentric cylinder Couette cell, we have measured flow-induced displacements down to a few hundreds of nanometers, allowing the observation of the solid-to-liquid transition of a glassy system. We envisage new possibilities for NMR velocimetry as an experimental tool for colloidal chemistry and physics.

Journal Article↗

PubMed2003

Probing protein hydration and aging of food materials by the magnetic field dependence of proton spin-lattice relaxation times.

Most cheeses can be considered as solid emulsions of milk fat in a matrix of water and proteins. Regions of each of the phases can be liquid during processing and maturation. Identifying these regions and monitoring changes in them is important as a prelude to controlling the structure of the final cheese. We concentrate on the behavior of water in the vicinity of proteins as a function of cheese aging. Our method utilizes nuclear magnetic relaxation dispersion (NMRD) associated with the frequency dependence of water spin-lattice relaxation rates using the field cycling NMR technique. This method provides insight into the dynamical behavior of water molecules on a very large time scale. Moreover, we can distinguish between molecular motion in bulk and motion in the vicinity of a source of relaxation, such as proteins. A fit of our dispersion data using a theory developed by J.-P. Korb and R.G. Bryant (J. Chem. Phys. 115 (2001) 23) allowed us to determine the degree of hydration of proteins as a function of aging. In particular, we find that protein hydration increases with ripening.

Cheese↗