A proton nuclear magnetic resonance relaxation study of the glycine, alanine, and lactate complexes of gadolinium(III) in aqueous solution

1987 ◽  
Vol 65 (7) ◽  
pp. 1508-1512 ◽  
Author(s):  
R. Stephen Reid ◽  
Benjamin Podányi

The 1H nuclear magnetic resonance spin-lattice and spin–spin relaxation rate enhancements induced by the gadolinium(III) ion were measured in solutions of glycine, alanine, and sodium lactate containing different amounts of Gd(III). The proton relaxation rates in the Gd(III) complexes were calculated from these data, and were used to calculate metal–hydrogen atom distances. Comparison of these data with corresponding distances calculated from literature X-ray crystallographic data for model compounds shows that in the two amino acid complexes the Gd(III) ion is coordinated in a four-membered ring through the two oxygen atoms of the carboxylate group. By contrast, in the lactate complex coordination is via a five-membered ring involving one oxygen atom of the carboxylate group and the α-hydroxyl oxygen.

2018 ◽  
Vol 5 (7) ◽  
pp. 180221 ◽  
Author(s):  
R. J. Foster ◽  
R. A. Damion ◽  
M. E. Ries ◽  
S. W. Smye ◽  
D. G. McGonagle ◽  
...  

Samples of human and bovine cartilage have been examined using magnetic resonance imaging to determine the proton nuclear magnetic resonance spin–lattice relaxation time, T 1 , as a function of depth within through the cartilage tissue. T 1 was measured at five to seven temperatures between 8 and 38°C. From this, it is shown that the T 1 relaxation time is well described by Arrhenius-type behaviour and the activation energy of the relaxation process is quantified. The activation energy within the cartilage is approximately 11 ± 2 kJ mol −1 with this notably being less than that for both pure water (16.6 ± 0.4 kJ mol −1 ) and the phosphate-buffered solution in which the cartilage was immersed (14.7 ± 1.0 kJ mol −1 ). It is shown that this activation energy increases as a function of depth in the cartilage. It is known that cartilage composition varies with depth, and hence, these results have been interpreted in terms of the structure within the cartilage tissue and the association of the water with the macromolecular constituents of the cartilage.


2016 ◽  
Vol 3 (3) ◽  
pp. 150705 ◽  
Author(s):  
Richard J. Foster ◽  
Robin A. Damion ◽  
Thomas G. Baboolal ◽  
Stephen W. Smye ◽  
Michael E. Ries

Aggrecan, a highly charged macromolecule found in articular cartilage, was investigated in aqueous salt solutions with proton nuclear magnetic resonance. The longitudinal and transverse relaxation rates were determined at two different field strengths, 9.4 T and 0.5 T, for a range of temperatures and aggrecan concentrations. The diffusion coefficients of the water molecules were also measured as a function of temperature and aggrecan concentration, using a pulsed field gradient technique at 9.4 T. Assuming an Arrhenius relationship, the activation energies for the various relaxation processes and the translational motion of the water molecules were determined from temperature dependencies as a function of aggrecan concentration in the range 0–5.3% w/w. The longitudinal relaxation rate and inverse diffusion coefficient were approximately equally dependent on concentration and only increased by upto 20% from that of the salt solution. The transverse relaxation rate at high field demonstrated greatest concentration dependence, changing by an order of magnitude across the concentration range examined. We attribute this primarily to chemical exchange. Activation energies appeared to be approximately independent of aggrecan concentration, except for that of the low-field transverse relaxation rate, which decreased with concentration.


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