Observation of quadrupole spin echo after a single pulse for application of a two-frequency signal in KReO4

1975 ◽  
Vol 18 (4) ◽  
pp. 446-447
Author(s):  
N. E. Ainbinder ◽  
A. S. Kim
1994 ◽  
Vol 40 (7) ◽  
pp. 1245-1250 ◽  
Author(s):  
R A Wevers ◽  
U Engelke ◽  
A Heerschap

Abstract Although spin-echo techniques are often used to obtain 1H-NMR spectra of serum or plasma samples, they do not provide reliable quantitative analyses of metabolites. We present a standardized procedure, optimized for sensitivity, for using single-pulse 1H-NMR spectroscopy to analyze deproteinized plasma. The detection limit for various metabolites ranges between 2 and 40 mumol/L. The method allows quantitative analysis of many compounds of interest in studies of inborn errors of metabolism, including betaine and dimethylglycine, which cannot be measured easily with other techniques. For lactate, tyrosine, threonine, and alanine, we obtained results that correlated well with those obtained by established techniques. We also present a library containing resonance positions of 38 compounds occurring in plasma samples in health and disease, including 14 as-yet-unidentified resonances. As an example of the diagnostic power of the technique we show a spectrum of a plasma sample from a patient with 5-oxoprolinuria (pyroglutamic aciduria; McKusick 266130), an enzymatic defect in glutathione biosynthesis.


1995 ◽  
Vol 50 (10) ◽  
pp. 942-948
Author(s):  
Fritz Schick

Abstract From 100 ml spherical glass bottles filled with aqueous solutions and suspended in a homogeneous magnetic field, NMR spectra with linewidths of about 0.7 Hz were achieved in single-pulse and multi-pulse spectra. A relatively wide receiver coil as the body coil or the standard head coil of the manufacturer were employed to acquire spectra after different non-localized pulse sequences. Examples of single-pulse spectra and double spin-echo spectra of aqueous solutions with lactate, citrate, or glucose are demonstrated and discussed. The fact that all experiments can be performed using well-defined pulse angles acting on the entire sample at the field strenght of the whole-body unit allows to determine the characteristics (e.g. chemical shift differences, coupling constants) of spin systems of biologically important molecules precisely, without need for additional spectrometers. Constant flip angles are advantageous for adequate theoretical analysis of spectra from coupled spin systems. The effects of a defined "misadjustment" of the transmitter on the spectra can be measured directly, whereas localized methods always yield a superposition of signals due to the distribution of flip angles inside the selected volume. In some cases, optimized sequence parameters for localized examinations in vivo can be derived numerically from the analyzed coupling data.


1998 ◽  
Vol 57 (18) ◽  
pp. 11554-11564 ◽  
Author(s):  
I. G. Kiliptari ◽  
V. I. Tsifrinovich
Keyword(s):  

1969 ◽  
Vol 12 (9) ◽  
pp. 1121-1122
Author(s):  
V. S. Grechishkin ◽  
E. M. Shishkin

1979 ◽  
Vol 22 (11) ◽  
pp. 978-979
Author(s):  
N. E. Ainbinder ◽  
A. S. Azheganov ◽  
A. S. Kim
Keyword(s):  

JETP Letters ◽  
2007 ◽  
Vol 86 (5) ◽  
pp. 337-339 ◽  
Author(s):  
E. A. Kravchenko ◽  
V. G. Morgunov ◽  
V. G. Orlov ◽  
Yu. F. Kargin

1986 ◽  
Vol 41 (1-2) ◽  
pp. 449-452
Author(s):  
Narsimha Reddy ◽  
Arun Bhavsar ◽  
P. T. Narasimhan

A simple microprocessor-controlled pulsed NQR spectrometer system has been developed with the capability to acquire Zeeman perturbed spin echo envelope modulations (ZSEEM). The CPU of the system is based on the Intel Corporation 8085 A microprocessor. The performance of the spectrometer is illustrated with the presentation of ZSEEM spectra of NaClO3 and KClO3.


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