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Related Concept Videos

Double Resonance Techniques: Overview01:12

Double Resonance Techniques: Overview

873
Double resonance techniques in Nuclear Magnetic Resonance (NMR) spectroscopy involve the simultaneous application of two different frequencies or radiofrequency pulses to manipulate and observe two distinct nuclear spins. One important application of double resonance is spin decoupling, which selectively suppresses coupling with one type of nucleus while observing the NMR signal from another nucleus, simplifying the spectrum and enhancing resolution.
Spin decoupling is usually achieved by...
873
NMR Spectrometers: Resolution and Error Correction01:14

NMR Spectrometers: Resolution and Error Correction

1.2K
When magnetic nuclei in a sample achieve resonance and undergo relaxation, the signal detected in NMR is an approximately exponential free induction decay. Fourier transform of an exponential decay yields a Lorentzian peak in the frequency domain. Lorentzian peaks in an NMR spectrum are defined by their amplitude, full width at half maximum, and position, where the peak width is governed by the spin-spin relaxation time alone. In real experiments, however, the applied magnetic field is rendered...
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Proton (¹H) NMR: Chemical Shift01:07

Proton (¹H) NMR: Chemical Shift

4.4K
Organic molecules primarily contain carbon and hydrogen atoms. While all the hydrogen isotopes are NMR-active, protium or hydrogen-1 is the most abundant. It has a significant energy separation between its nuclear spin states due to its large gyromagnetic ratio. As per Boltzmann's distribution, an increase in the energy separation implies a greater excess population of nuclei available for excitation, resulting in a strong NMR absorption signal.
Absorption signals of all the protium nuclei...
4.4K
¹H NMR of Labile Protons: Temporal Resolution01:10

¹H NMR of Labile Protons: Temporal Resolution

1.8K
Protons bonded to heteroatoms such as nitrogen and oxygen exhibit a range of chemical shift values. This is due to the varying degree of hydrogen bonding between the proton and the heteroatom in other molecules. The extent of hydrogen bonding affects the electron density around the proton, thereby giving different chemical shift values for the protons in the proton NMR spectrum.
The –OH proton in alcohols typically appears in the range of δ 2 to 5 ppm but can vary depending on the...
1.8K
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)01:20

¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)

1.9K
When proton-coupled carbon-13 spectra are simplified by a broadband proton decoupling technique, structural information about the coupled protons is lost. Distortionless enhancement by polarization transfer (DEPT) is a technique that provides information on the number of hydrogens attached to each carbon in a molecule. While the DEPT experiment utilizes complex pulse sequences, the pulse delay and flip angle are specifically manipulated. The resulting signals have different phases depending on...
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Proton Transfer and Protein Conformation Dynamics in Photosensitive Proteins by Time-resolved Step-scan Fourier-transform Infrared Spectroscopy
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Accelerated model-based proton resonance frequency shift temperature mapping using echo-based GRAPPA reconstruction.

Feiyu Chen1, Xinwei Shi2, Shuo Chen3

  • 1Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China; Department of Electrical Engineering, Stanford University, CA, USA.

Magnetic Resonance Imaging
|December 3, 2014
PubMed
Summary
This summary is machine-generated.

This study introduces Echo-based GRAPPA, an accelerated method for MR temperature estimation using the proton resonance frequency shift. The new technique achieves acceleration factors of 2-3 with minimal temperature error, outperforming conventional GRAPPA.

Keywords:
AccelerationGRAPPAModel-based proton resonance frequency shiftTemperature mapping

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Area of Science:

  • Magnetic Resonance Imaging
  • Biomedical Engineering
  • Medical Physics

Background:

  • Accurate MR temperature estimation is crucial for various applications, including thermal ablation monitoring.
  • The proton resonance frequency (PRF) shift method is a common technique for MR thermometry.
  • Current methods can be time-consuming, necessitating acceleration strategies.

Purpose of the Study:

  • To develop and validate an accelerated MR temperature estimation method.
  • To utilize a model-based PRF shift approach with enhanced speed.
  • To assess the accuracy of the proposed acceleration technique.

Main Methods:

  • A multi-echo gradient-recalled echo (GRE) sequence was used to acquire images at 16 echo times (TE).
  • Retrospective undersampling of k-space data was performed at reduction factors of 2-3.
  • A novel reconstruction method, Echo-based GRAPPA, combined data from three TEs for accelerated imaging.

Main Results:

  • Echo-based GRAPPA achieved a reconstruction-induced temperature Root Mean Square Error (RMSE) below 1.4 °C in ex vivo liver experiments (reduction factor 2.3).
  • In vivo breast imaging demonstrated a mean temperature error of 2.3 °C in water-fat mixed regions (reduction factor 2.7).
  • The proposed Echo-based GRAPPA method showed lower temperature RMSE compared to conventional GRAPPA.

Conclusions:

  • The developed Echo-based GRAPPA method effectively accelerates MR temperature estimation using the model-based PRF shift.
  • The technique achieves acceleration factors of 2-3 with temperature errors below 3°C in relevant imaging scenarios.
  • This acceleration holds promise for improving the efficiency of MR thermometry.