Deuterium and phosphorus-31 nuclear magnetic resonance of cholesteryl palmitate in dipalmitoylphosphatidylcholine model membranes

1980 ◽  
Vol 58 (23) ◽  
pp. 2433-2441 ◽  
Author(s):  
Robert J. Cushley ◽  
Heiner Gorrissen ◽  
Stephen R. Wassall
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Liquid Crystalline ◽  
Acyl Chain ◽  
Relaxation Times ◽  
Average Diameter ◽  
Low Degree ◽  
Cholesteryl Palmitate ◽  
Degree Of Order ◽  
Ester Chain

Cholesteryl palmitate (CP) bas been incorporated into vesicles of dipalmitoylphosphatidylcholine and dipalmitoylphosphatidylcholine/20 mol% cholesterol, in amounts up to 5 mol%. By means of 31P lanthanide induced shifts the average diameter of these vesicles was calculated to be ~270 Å.The 2H spectral linewidths of selectively deuterated CP incorporated into liquid crystalline dipalmitoylphosphatidylcholine vesicles are ≤ 150 Hz, implying a low degree of order for the ester acyl chain. Addition of 20 mol% cholesterol to the vesicles increases the linewidths which, nevertheless, remain ≤ 185 Hz. The corresponding 2H longitudinal relaxation times (≤ 450 ms) indicate that the fast segmental motions of the ester chain are slower than for the phospholipid chains.

An emerging technology: Nuclear magnetic resonance microscopy

1988 ◽  
Vol 46 ◽  
pp. 1000-1001
Author(s):  
M.J. Hennessy ◽  
E. Kwok
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Relaxation Times ◽  
Basic Research ◽  
Local Environment ◽  
Magnetic Resonance Images ◽  
Nmr Microscopy ◽  
Mri Scans ◽  
Temperature Relaxation ◽  
Nuclear Magnetic

Much progress in nuclear magnetic resonance microscope has been made in the last few years as a result of improved instrumentation and techniques being made available through basic research in magnetic resonance imaging (MRI) technologies for medicine. Nuclear magnetic resonance (NMR) was first observed in the hydrogen nucleus in water by Bloch, Purcell and Pound over 40 years ago. Today, in medicine, virtually all commercial MRI scans are made of water bound in tissue. This is also true for NMR microscopy, which has focussed mainly on biological applications. The reason water is the favored molecule for NMR is because water is,the most abundant molecule in biology. It is also the most NMR sensitive having the largest nuclear magnetic moment and having reasonable room temperature relaxation times (from 10 ms to 3 sec). The contrast seen in magnetic resonance images is due mostly to distribution of water relaxation times in sample which are extremely sensitive to the local environment.

Textural and pore size analysis of carbonates from integrated core and nuclear magnetic resonance logging: An Arbuckle study

2015 ◽  
Vol 3 (1) ◽  
pp. SA77-SA89 ◽  
Author(s):  
John Doveton ◽  
Lynn Watney
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Relaxation Time ◽  
Magnetic Resonance ◽  
Pore Size ◽  
Relaxation Times ◽  
T2 Relaxation Time ◽  
T2 Relaxation ◽  
Nmr Logging ◽  
The Core ◽  
Nuclear Magnetic

The T2 relaxation times recorded by nuclear magnetic resonance (NMR) logging are measures of the ratio of the internal surface area to volume of the formation pore system. Although standard porosity logs are restricted to estimating the volume, the NMR log partitions the pore space as a spectrum of pore sizes. These logs have great potential to elucidate carbonate sequences, which can have single, double, or triple porosity systems and whose pores have a wide variety of sizes and shapes. Continuous coring and NMR logging was made of the Cambro-Ordovician Arbuckle saline aquifer in a proposed CO2 injection well in southern Kansas. The large data set gave a rare opportunity to compare the core textural descriptions to NMR T2 relaxation time signatures over an extensive interval. Geochemical logs provided useful elemental information to assess the potential role of paramagnetic components that affect surface relaxivity. Principal component analysis of the T2 relaxation time subdivided the spectrum into five distinctive pore-size classes. When the T2 distribution was allocated between grainstones, packstones, and mudstones, the interparticle porosity component of the spectrum takes a bimodal form that marks a distinction between grain-supported and mud-supported texture. This discrimination was also reflected by the computed gamma-ray log, which recorded contributions from potassium and thorium and therefore assessed clay content reflected by fast relaxation times. A megaporosity class was equated with T2 relaxation times summed from 1024 to 2048 ms bins, and the volumetric curve compared favorably with variation over a range of vug sizes observed in the core. The complementary link between grain textures and pore textures was fruitful in the development of geomodels that integrates geologic core observations with petrophysical log measurements.

Centerband-only-detection-of-exchange 31P nuclear magnetic resonance and phospholipid lateral diffusion: theory, simulation and experiment

2015 ◽  
Vol 17 (38) ◽  
pp. 25160-25171 ◽  
Author(s):  
Angel Lai ◽  
Qasim Saleem ◽  
Peter M. Macdonald
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Diffusion Coefficient ◽  
Magnetic Resonance ◽  
Liquid Crystalline ◽  
Diffusion Theory ◽  
Lateral Diffusion ◽  
Liquid Crystalline Phases ◽  
Simulation And Experiment ◽  
Spherical Vesicles ◽  
Lateral Diffusion Coefficient

Theory of CODEX 31P NMR lateral diffusion coefficient measurements on phospholipids in spherical vesicles is described and used to simulate experimental results on DMPC in both the gel and liquid-crystalline phases.

scholarly journals Preliminary magnetic resonance relaxometric analysis of Fricke gel dosimeters produced with polyvinyl alcohol and glutaraldehyde

2017 ◽  
Vol 32 (3) ◽  
pp. 242-249 ◽  
Author(s):  
Salvatore Gallo ◽  
Giorgio Collura ◽  
Giuseppina Iacoviello ◽  
Anna Longo ◽  
Luigi Tranchina ◽  
...  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Polyvinyl Alcohol ◽  
Dose Range ◽  
Relaxation Times ◽  
Ion Concentration ◽  
Nuclear Magnetic Resonance Relaxometry ◽  
New Formulation ◽  
Nuclear Magnetic

This work describes the preliminary analysis of Fricke gels dosimeters characterized by a new formulation making use of a matrix of polyvinyl alcohol cross-linked by adding glutaraldehyde and analyzed by means of nuclear magnetic resonance relaxometry. In previous optical studies, these gels have shown promising dosimetric features in terms of photon sensitivity and low diffusion of ferric ions produced after irradiation. In this work, we used a portable nuclear magnetic resonance relaxometer to measure the relaxation times (which are important for dosimetric applications) of these gel materials. For this purpose, we performed a study for optimizing the acquisition parameters with a nuclear magnetic resonance relaxometer. Gel samples were exposed to clinical 6 MV photons in the dose range between 0 and 20 Gy. Nuclear magnetic resonance relaxometry measurements were per- formed and the sensitivity to photon beams was measured for various values of the Fe2+ ion concentration. The analyses pointed out that the MR signal increases as the Fe2+ content in- creases and the increase is about 75 % when the concentration of Fe2+ ions is increased from 0.5 mM to 2.5 mM. Furthermore, the sensitivity improvement achieved with increasing the Fe2+ concentration is about 60 %. This paper shows that the portable nuclear magnetic resonance relaxometer used for analysis of porous materials can be used for characterization of these dosimetric gels and this study can be considered as the first step for the characterization of these dosimeters which in future could be used for 3-D dose mapping in clinical applications.

Nuclear magnetic resonance microscopy of single neurons under hypotonic perturbation

1996 ◽  
Vol 271 (6) ◽  
pp. C1895-C1900 ◽  
Author(s):  
E. W. Hsu ◽  
N. R. Aiken ◽  
S. J. Blackband
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Single Cells ◽  
Extracellular Volume ◽  
Relaxation Times ◽  
Volume Ratio ◽  
Cell Swelling ◽  
Single Neurons ◽  
Apparent Diffusion Coefficients ◽  
Nuclear Magnetic

Nuclear magnetic resonance (NMR) characteristics of water in perfused single neurons undergoing a 20% hypotonic perturbation were examined quantitatively using NMR microscopy. The transverse relaxation times (T2) in the cytoplasm and nucleus increased by 24.0 +/- 8.5% (average +/- SE, n = 8) and 29.7 +/- 5.3% (n = 6), respectively, whereas the apparent diffusion coefficients (ADC) showed no significant change. These findings are consistent with the behaviors of a perfect osmometer and with accepted molecular relaxation and diffusion models and have significant impacts on current views of properties of cellular water. Furthermore, the results suggest that the increase of tissue intracellular-to-extracellular volume ratio during cell swelling is the predominant mechanism underlying the ADC reduction in acute brain ischemia. These data are the first direct quantitative measurements of the NMR characteristics of water in the cytoplasm and nucleus of single cells undergoing physiological perturbations and may lead to an improved diagnostic capability for NMR imaging in a variety of disease states.

A nuclear magnetic resonance investigation of n -pentane, n -hexane and cyclo pentane

1954 ◽  
Vol 222 (1151) ◽  
pp. 526-541 ◽  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Molecular Motion ◽  
Relaxation Times ◽  
Lattice Relaxation ◽  
Spin Lattice Relaxation ◽  
Kcal Mole ◽  
Second Moment ◽  
Spin Lattice ◽  
Second Moments

The nuclear magnetic resonance spectra and spin-lattice relaxation times have been measured for the protons in n -pentane (C 5 H 12 ), n -hexane (C 6 H 14 ) and cyclo pentane (C 5 H 10 ) all in the solid state. The temperature range covered was from 70° K to the melting-points of 143·4° K for n -pentane, 177·8° K for n -hexane and 179·4° K for cyclo pentane. In the case of n -pentane and n -hexane the second moments of the absorption lines were found to be smaller than the computed rigid lattice values over the. whole temperature range. Possible molecular motions which might cause this reduction are discussed. It is suggested that the most probable type of motion is reorientation of the methyl groups at the ends of each molecule about the adjacent C—C bonds. An analysis of the spin-lattice relaxation times shows that this reorientation process is governed by an activation energy of 2·7 kcal/mole for n -pentane and 2·9 kcal/mole for n -hexane, values which support the mechanism postulated. At the lowest temperature the absorption lines had not reached their full widths, even though the reorientation frequencies at these temperatures were considerably less than the line-widths. The experimental second moment for cyclo pentane below about 120° K indicates that the lattice is effectively rigid in this temperature region. The uncertainties in both the experimental and theoretical second moments do not allow a distinction to be drawn between the plane and puckered molecular models. At the temperature of the first transition (122·4° K) the line-width second moment and relaxation time all show a sudden decrease. The low value of second moment at the higher temperatures indicates that considerable molecular motion is occurring, the molecules rotating with spherical symmetry. The change in crystal structure at the temperature of the second transition (138·1° K) is thought to be a direct result of this spherical symmetry. As the temperature increases, the results indicate that more molecular motion must be occurring, and it is thought that the rotating molecules are diffusing through the lattice.

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