Resolution enhancement in MRI.

We consider the problem of super-resolution reconstruction (SRR) in MRI. Subpixel-shifted MR images were taken in several fields of view (FOVs) to reconstruct a high-resolution image. A novel algorithm is presented.

17O magnetic resonance imaging of the human brain.

Here we show the first example of in vivo oxygen-17 (17O) magnetic resonance imaging of the human in natural abundance. Two-dimensional fast multi-planar gradient recalled 90 deg echo (FMPGR/90) pulse sequence and three-dimensional projection reconstruction pulse sequence methods were used.

Magnetic field gradients in the MRI suite and their effects on aneurysm clips.

We studied magnetic field intensity in the magnetic resonance imaging suite at our hospital and its possible effect on several different types of aneurysm clips, including one Heifetz 17-7 PH, six Heifetz Elgiloy, one Mayfield, six Perneczky, fifteen Sugita, one Sundt-Kees Variangle, four Variangle-McFadden and fifteen Yasargil clips. We carefully observed the clips for any translational or rotational movements along the path from the door towards the magnetic resonance imaging gantry. The magnetic field strength was 0.

Determination of regional cerebral oxygen consumption in the human: 17O natural abundance cerebral magnetic resonance imaging and spectroscopy in a whole body system.

17O natural abundance imaging in a whole body imager is demonstrated using standard MRI spectrometer and 1H imaging methods. A novel design of a highly sensitive 17O/1H doubly tuned surface head coil is shown. The head probe allows simultaneous acquisition of 17O and 1H images using a single coil.

Determination of the rate of cerebral oxygen consumption and regional cerebral blood flow by non-invasive 17O in vivo NMR spectroscopy and magnetic resonance imaging. Part 2. Determination of CMRO2 for the rat by 17O NMR, and CMRO2, rCBF and the partition coefficient for the cat by 17O MRI.

The rate of oxygen consumption (CMRO2) in intact rat and cat brains was calculated by novel data analysis methods from data obtained in in vivo 17O NMR spectroscopy and imaging inhalation studies. Data analysis methods of 17O inhalation measurements are applied to the calculation of CMRO2, regional cerebral blood flow (rCBF), the reflow (R), the arterial venous difference (AVD) and the partition coefficient (lambda). Several of the applied methods for the determination of CMRO2 do not require measurements of regional cerebral blood flow and H2 17O arterial concentration.

Determination of the rate of cerebral oxygen consumption and regional cerebral blood flow by non-invasive 17O in vivo NMR spectroscopy and magnetic resonance imaging: Part 1. Theory and data analysis methods.

Theory and novel data analysis methods of 17O inhalation measurements are presented for the calculation of CMRO2, regional cerebral blood flow (rCBF), the reflow (R), the arterial venous difference (AVD) and the partition coefficient (lambda). Several of the methods proposed for the determination of CMRO2 do not require measurements of regional cerebral blood flow and H2(17)O arterial concentration. All methods of analysis are based on the Kety-Schmidt approach.

In vivo 17O NMR study of rat brain during 17O2 inhalation.

In vivo 17O NMR has been used to monitor the H2(17)O concentration in rat brain during inhalation of 17O2. The results are discussed in terms of oxygen consumption in the brain and recirculation into the brain of H2(17)O produced in other organs.

In vivo measurement of cerebral oxygen consumption and blood flow using 17O magnetic resonance imaging.

We used 17O NMR imaging techniques to measure the H2(17)O concentration in a 0.8-ml voxel in the cat brain following injection of an arterial bolus of enriched H2(17)O and during inhalation of enriched 17O2. We also measured the H2(17)O concentration in arterial blood during 17O2 inhalation.

17O, 14N and 15N n.m.r. studies of the Co2+ complexes of cyclo(Pro17O-Gly15N) and cyclo(Gly17O-Pro) in aqueous solution.

The complexation of cyclo(Pro17O-Gly15N) and cyclo(Gly17O-Pro) with Co2+ ions has been studied by 17O, 14N and 15N n.m.r.

Synthesis of 17O isotope labeled Leu-enkephalin and 17O n.m.r.

Oxygen-17 isotope was introduced into the alpha-carboxyl group of glycine, 1-phenylalanine, 1-leucine and 1-tyrosine by acid catalyzed exchange of 17O from H2O(17) or by acid hydrolysis of respective amino acid methyl esters in H2O(17). Quantitative enrichment of glycine was achieved by acid hydrolysis of amino acetonitrile in H2O(17). For alpha-amino protection in amino acids t-butoxycarbonyl (Boc) group was employed for 17O labeled enkephalin synthesis.

17O n.m.r. studies of amino acids in the solid state, in single- and polycrystalline forms.

A single crystal of 17O enriched alpha-glycine was grown by slow evaporation of aqueous solution. 17O n.m.

17O and 14N n.m.r. studies of the Co (II) interaction with cyclo(Ala*-Ala) in aqueous solution.

The complexation of cyclo(Ala*-Ala) with the cobaltous ions in aqueous solution was investigated by 17O and 14N n.m.r.

Oxygen-18 isotope labeling and its effect on carbon-13 chemical shifts of the peptide bond.

The effects of 18O isotopes on 13C NMR chemical shifts of peptide carbonyl carbons were found to be 0.028 ppm for glyclyglycine and 0.029 ppm for glycylproline at 50.

Isotopic labeling of tyrosine, followed by 17O n.m.r.

A simple chemical procedure has been developed in order to introduce oxygen-17 labels into the carboxylic and phenolic sites of L-tyrosine. Detailed studies of the 17O n.m.

17O NMR investigation of the hydration of L-alanine and L-proline in water/Me2SO mixtures.

The hydration state of L-Alanine and L-Proline has been assessed via 17O NMR. At neutral and basic pH, two water molecules are hydrogen bonded at the carboxylate group, one to each oxygen, whereas a third water molecule is hydrogen bonded to the protonated COOH group at acidic pH, via the hydroxyl hydrogen. The possible formation of dimers and/or higher complexes in DMSO is indicated not only from the chemical shift but also from the linewidth of the amino acids.

Oxygen-17 n.m.r. of peptides.

Peptide-17O chemical shifts of linear dipeptides with and without protecting groups in H2O, CH3OH, CH2Cl2, CHCl3, CCl4, CH3CN and DMSO were between 256-350 ppm downfield from external water. Increasing solvent H-bond donating ability correlated with shifts to higher field. The 17O resonance of several cyclic dipeptides appeared at higher field relative to comparable linear dipeptides (303-317 p.

Hydrogen bonds in the tripeptide Pro-Leu-Gly-NH2. 17O and 1H studies.

17O-NMR measurements of labeled Pro-Leu-Gly-NH2 were carried out at different pH levels and in mixed solvents of water/acetonitrile. Complementary studies of the amide protons were carried out in acetonitrile-d3. Only the prolyl C = 17O group was sensitive to the pH level.

Carbonyl-17O n.m.r. of amino acid and peptide carboxamide and methyl ester derivatives.

Specific carbonyl enrichment with 17O of amino acid OMe esters by up to 10(3) times over natural abundance was affected by treating [17O]-alpha-COOH amino acids with SOCl2 in MeOH. Carbonyl-[17O]-Gly-NH2, Gly-NHCH3 and Gly-N(CH3)2 were obtained from [17O]-Gly-OMe by (methyl)aminolysis with NH3, CH3NH2 and (CH3)2NH gases respectively. Peptide [17O]-carboxamides were prepared by (methyl)aminolysis of Z-Pro-Leu-[17O]-Gly-OMe followed by catalytic hydrogenation to remove the Z group.

Labeling of amino acids and peptides with isotopic oxygen as followed by 17O-N.M.R.

17O was introduced into the respective alpha- and gamma-COOH groups of Boc-Gly and Boc-Glu by saponification of the corresponding O-methyl esters with 1N NaOH in H2 17O. Other 17O enriched Boc-amino acids were prepared by acid catalyzed exchange into the amino acid alpha-COOH group followed by t-butyloxycarbonylation with t-butyl S-4, 6-dimethylpyrimidin-2-ylthio carbonate. Final enrichment, by approximately three orders of magnitude over natural abundance, was 60-100% of the possible maximum.