Details

In Vivo NMR Spectroscopy


In Vivo NMR Spectroscopy

Principles and Techniques
3. Aufl.

von: Robin A. de Graaf

120,99 €

Verlag: Wiley
Format: PDF
Veröffentl.: 11.12.2018
ISBN/EAN: 9781119382577
Sprache: englisch
Anzahl Seiten: 592

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Beschreibungen

<p><b>Presents basic concepts, experimental methodology and data acquisition, and processing standards of <i>in vivo</i> NMR spectroscopy</b></p> <p>This book covers, in detail, the technical and biophysical aspects of <i>in vivo</i> NMR techniques and includes novel developments in the field such as hyperpolarized NMR, dynamic <sup>13</sup>C NMR, automated shimming, and parallel acquisitions. Most of the techniques are described from an educational point of view, yet it still retains the practical aspects appreciated by experimental NMR spectroscopists. In addition, each chapter concludes with a number of exercises designed to review, and often extend, the presented NMR principles and techniques.</p> <p>The third edition of <i>In Vivo NMR Spectroscopy: Principles and Techniques</i> has been updated to include experimental detail on the developing area of hyperpolarization; a description of the semi-LASER sequence, which is now a method of choice; updated chemical shift data, including the addition of <sup>31</sup>P data; a troubleshooting section on common problems related to shimming, water suppression, and quantification; recent developments in data acquisition and processing standards; and MatLab scripts on the accompanying website for helping readers calculate radiofrequency pulses.</p> <ul> <li>Provide an educational explanation and overview of <i>in vivo</i> NMR, while maintaining the practical aspects appreciated by experimental NMR spectroscopists</li> <li>Features more experimental methodology than the previous edition</li> <li>End-of-chapter exercises that help drive home the principles and techniques and offer a more in-depth exploration of quantitative MR equations</li> <li>Designed to be used in conjunction with a teaching course on the subject</li> </ul> <p><i>In Vivo NMR Spectroscopy: Principles and Techniques, 3<sup>rd</sup> Edition</i> is aimed at all those involved in fundamental and/or diagnostic <i>in vivo</i> NMR, ranging from people working in dedicated <i>in vivo</i> NMR institutes, to radiologists in hospitals, researchers in high-resolution NMR and MRI, and in areas such as neurology, physiology, chemistry, and medical biology.</p> <p> </p>
<p>Preface xv</p> <p>Abbreviations xvii</p> <p>Supplementary Material xxiv</p> <p><b>1 Basic Principles </b><b>1</b></p> <p>1.1 Introduction 1</p> <p>1.2 Classical Magnetic Moments 3</p> <p>1.3 Nuclear Magnetization 5</p> <p>1.4 Nuclear Induction 9</p> <p>1.5 Rotating Frame of Reference 11</p> <p>1.6 Transverse T2 and T2 * Relaxation 12</p> <p>1.7 Bloch Equations 16</p> <p>1.8 Fourier Transform NMR 17</p> <p>1.9 Chemical Shift 20</p> <p>1.10 Digital NMR 23</p> <p>1.10.1 Analog‐to‐digital Conversion 23</p> <p>1.10.2 Signal Averaging 25</p> <p>1.10.3 Digital Fourier Transformation 25</p> <p>1.10.4 Zero Filling 25</p> <p>1.10.5 Apodization 26</p> <p>1.11 Quantum Description of NMR 28</p> <p>1.12 Scalar Coupling 30</p> <p>1.13 Chemical and Magnetic Equivalence 33</p> <p>Exercises 37</p> <p>References 40</p> <p><b>2 </b><b>In Vivo </b><b>NMR Spectroscopy – Static Aspects </b><b>43</b></p> <p>2.1 Introduction 43</p> <p>2.2 Proton NMR Spectroscopy 43</p> <p>2.2.1 Acetate (Ace) 51</p> <p>2.2.2 N‐Acetyl Aspartate (NAA) 52</p> <p>2.2.3 N‐Acetyl Aspartyl Glutamate (NAAG) 53</p> <p>2.2.4 Adenosine Triphosphate (ATP) 54</p> <p>2.2.5 Alanine (Ala) 55</p> <p>2.2.6 γ‐Aminobutyric Acid (GABA) 56</p> <p>2.2.7 Ascorbic Acid (Asc) 57</p> <p>2.2.8 Aspartic Acid (Asp) 58</p> <p>2.2.9 Branched‐chain Amino Acids (Isoleucine, Leucine, and Valine) 58</p> <p>2.2.10 Choline‐containing Compounds (tCho) 59</p> <p>2.2.11 Creatine (Cr) and Phosphocreatine (PCr) 61</p> <p>2.2.12 Ethanol 62</p> <p>2.2.13 Ethanolamine (EA) and Phosphorylethanolamine (PE) 63</p> <p>2.2.14 Glucose (Glc) 63</p> <p>2.2.15 Glutamate (Glu) 64</p> <p>2.2.16 Glutamine (Gln) 65</p> <p>2.2.17 Glutathione (GSH) 66</p> <p>2.2.18 Glycerol 67</p> <p>2.2.19 Glycine 68</p> <p>2.2.20 Glycogen 68</p> <p>2.2.21 Histidine 69</p> <p>2.2.22 Homocarnosine 70</p> <p>2.2.23 β‐Hydoxybutyrate (BHB) 70</p> <p>2.2.24 2‐Hydroxyglutarate (2HG) 71</p> <p>2.2.25 myo‐Inositol (mI) and scyllo‐Inositol (sI) 72</p> <p>2.2.26 Lactate (Lac) 73</p> <p>2.2.27 Macromolecules 74</p> <p>2.2.28 Nicotinamide Adenine Dinucleotide (NAD+) 76</p> <p>2.2.29 Phenylalanine 76</p> <p>2.2.30 Pyruvate 77</p> <p>2.2.31 Serine 78</p> <p>2.2.32 Succinate 79</p> <p>2.2.33 Taurine (Tau) 79</p> <p>2.2.34 Threonine (Thr) 80</p> <p>2.2.35 Tryptophan (Trp) 80</p> <p>2.2.36 Tyrosine (Tyr) 80</p> <p>2.2.37 Water 81</p> <p>2.2.38 Non‐cerebral Metabolites 82</p> <p>2.2.39 Carnitine and Acetyl‐carnitine 82</p> <p>2.2.40 Carnosine 84</p> <p>2.2.41 Citric Acid 86</p> <p>2.2.42 Deoxymyoglobin (DMb) 87</p> <p>2.2.43 Lipids 87</p> <p>2.2.44 Spermine and Polyamines 89</p> <p>2.3 Phosphorus‐31 NMR Spectroscopy 90</p> <p>2.3.1 Chemical Shifts 90</p> <p>2.3.2 Intracellular pH 92</p> <p>2.4 Carbon‐13 NMR Spectroscopy 93</p> <p>2.4.1 Chemical Shifts 93</p> <p>2.5 Sodium‐23 NMR Spectroscopy 96</p> <p>2.6 Fluorine‐19 NMR Spectroscopy 102</p> <p>2.7 In vivo NMR on Other Non‐proton Nuclei 104</p> <p>Exercises 106</p> <p>References 108</p> <p><b>3 </b><b>In Vivo </b><b>NMR Spectroscopy – Dynamic Aspects </b><b>129</b></p> <p>3.1 Introduction 129</p> <p>3.2 Relaxation 129</p> <p>3.2.1 General Principles of Dipolar Relaxation 129</p> <p>3.2.2 Nuclear Overhauser Effect 133</p> <p>3.2.3 Alternative Relaxation Mechanisms 134</p> <p>3.2.4 Effects of T1 Relaxation 137</p> <p>3.2.5 Effects of T2 Relaxation 138</p> <p>3.2.6 Measurement of T1 and T2 Relaxation 141</p> <p>3.2.6.1 T1 Relaxation 141</p> <p>3.2.6.2 Inversion Recovery 141</p> <p>3.2.6.3 Saturation Recovery 142</p> <p>3.2.6.4 Variable Nutation Angle 142</p> <p>3.2.6.5 MR Fingerprinting 143</p> <p>3.2.6.6 T2 Relaxation 143</p> <p>3.2.7 In Vivo Relaxation 144</p> <p>3.3 Magnetization Transfer 147</p> <p>3.3.1 Principles of MT 149</p> <p>3.3.2 MT Methods 150</p> <p>3.3.3 Multiple Exchange Reactions 152</p> <p>3.3.4 MT Contrast 152</p> <p>3.3.5 Chemical Exchange Saturation Transfer (CEST) 156</p> <p>3.4 Diffusion 160</p> <p>3.4.1 Principles of Diffusion 160</p> <p>3.4.2 Diffusion and NMR 160</p> <p>3.4.3 Anisotropic Diffusion 169</p> <p>3.4.4 Restricted Diffusion 173</p> <p>3.5 Dynamic NMR of Isotopically‐Enriched Substrates 175</p> <p>3.5.1 General Principles and Setup 177</p> <p>3.5.2 Metabolic Modeling 177</p> <p>3.5.3 Thermally Polarized Dynamic 13C NMR Spectroscopy 184</p> <p>3.5.3.1 [1‐13C]‐Glucose and [1,6‐13C2]‐Glucose 184</p> <p>3.5.3.2 [2‐13C]‐Glucose 185</p> <p>3.5.3.3 [U‐13C6]‐Glucose 187</p> <p>3.5.3.4 [2‐13C]‐Acetate 187</p> <p>3.5.4 Hyperpolarized Dynamic 13C NMR Spectroscopy 189</p> <p>3.5.4.1 Brute Force Hyperpolarization 189</p> <p>3.5.4.2 Optical Pumping of Noble Gases 190</p> <p>3.5.4.3 Parahydrogen‐induced Polarization (PHIP) 191</p> <p>3.5.4.4 Signal Amplification by Reversible Exchange (SABRE) 193</p> <p>3.5.4.5 Dynamic Nuclear Polarization (DNP) 193</p> <p>3.5.5 Deuterium Metabolic Imaging (DMI) 196</p> <p>Exercises 197</p> <p>References199</p> <p><b>4 Magnetic Resonance Imaging </b><b>211</b></p> <p>4.1 Introduction 211</p> <p>4.2 Magnetic Field Gradients 211</p> <p>4.3 Slice Selection 212</p> <p>4.4 Frequency Encoding 215</p> <p>4.4.1 Principle 215</p> <p>4.4.2 Echo Formation 216</p> <p>4.5 Phase Encoding 219</p> <p>4.6 Spatial Frequency Space 221</p> <p>4.7 Fast MRI Sequences 225</p> <p>4.7.1 Reduced TR Methods 225</p> <p>4.7.2 Rapid k‐Space Traversal 226</p> <p>4.7.3 Parallel MRI 229</p> <p>4.7.3.1 SENSE 230</p> <p>4.7.3.2 GRAPPA 233</p> <p>4.8 Contrast in MRI 234</p> <p>4.8.1 T1 and T2 Relaxation Mapping 236</p> <p>4.8.2 Magnetic Field B0 Mapping 239</p> <p>4.8.3 Magnetic Field B1 Mapping 241</p> <p>4.8.4 Alternative Image Contrast Mechanisms 242</p> <p>4.8.5 Functional MRI 243</p> <p>Exercises 245</p> <p>References 249</p> <p><b>5 Radiofrequency Pulses 253</b></p> <p>5.1 Introduction 253</p> <p>5.2 Square RF Pulses 253</p> <p>5.3 Selective RF Pulses 259</p> <p>5.3.1 Fourier‐transform‐based RF Pulses 260</p> <p>5.3.2 RF Pulse Characteristics 262</p> <p>5.3.3 Optimized RF Pulses 266</p> <p>5.3.4 Multifrequency RF Pulses 269</p> <p>5.4 Composite RF Pulses 271</p> <p>5.5 Adiabatic RF Pulses 273</p> <p>5.5.1 Rotating Frame of Reference 275</p> <p>5.5.2 Adiabatic Condition 276</p> <p>5.5.3 Modulation Functions 278</p> <p>5.5.4 AFP Refocusing 280</p> <p>5.5.5 Adiabatic Plane Rotation of Arbitrary Nutation Angle 282</p> <p>5.6 Multidimensional RF Pulses 284</p> <p>5.7 Spectral–Spatial RF Pulses 284</p> <p>Exercises 286</p> <p>References 288</p> <p><b>6 Single Volume Localization and Water Suppression </b><b>293</b></p> <p>6.1 Introduction 293</p> <p>6.2 Single‐volume Localization 294</p> <p>6.2.1 Image Selected In Vivo Spectroscopy (ISIS) 295</p> <p>6.2.2 Chemical Shift Displacement 297</p> <p>6.2.3 Coherence Selection 301</p> <p>6.2.3.1 Phase Cycling 302</p> <p>6.2.3.2 Magnetic Field Gradients 302</p> <p>6.2.4 STimulated Echo Acquisition Mode (STEAM) 304</p> <p>6.2.5 Point Resolved Spectroscopy (PRESS) 307</p> <p>6.2.6 Signal Dephasing with Magnetic Field Gradients 309</p> <p>6.2.7 Localization by Adiabatic Selective Refocusing (LASER) 314</p> <p>6.3 Water Suppression 317</p> <p>6.3.1 Binomial and Related Pulse Sequences 318</p> <p>6.3.2 Frequency‐Selective Excitation 321</p> <p>6.3.3 Frequency‐Selective Refocusing 323</p> <p>6.3.4 Relaxation‐Based Methods 323</p> <p>6.3.5 Non‐water‐suppressed NMR Spectroscopy 326</p> <p>Exercises 327</p> <p>References 330</p> <p><b>7 Spectroscopic Imaging and Multivolume Localization </b><b>335</b></p> <p>7.1 Introduction 335</p> <p>7.2 Principles of MRSI 335</p> <p>7.3 k‐Space Description of MRSI 338</p> <p>7.4 Spatial Resolution in MRSI 339</p> <p>7.5 Temporal Resolution in MRSI 341</p> <p>7.5.1 Conventional Methods 343</p> <p>7.5.1.1 Circular and Spherical k‐Space Sampling 343</p> <p>7.5.1.2 k‐Space Apodization During Acquisition 343</p> <p>7.5.1.3 Zoom MRSI 345</p> <p>7.5.2 Methods Based on Fast MRI 346</p> <p>7.5.2.1 Echo‐planar Spectroscopic Imaging (EPSI) 346</p> <p>7.5.2.2 Spiral MRSI 349</p> <p>7.5.2.3 Parallel MRSI 350</p> <p>7.5.3 Methods Based on Prior Knowledge 351</p> <p>7.6 Lipid Suppression 353</p> <p>7.6.1 Relaxation‐based Methods 353</p> <p>7.6.2 Inner Volume Selection and Volume Prelocalization 355</p> <p>7.6.3 Outer Volume Suppression (OVS) 357</p> <p>7.7 MR Spectroscopic Image Processing and Display 360</p> <p>7.8 Multivolume Localization 364</p> <p>7.8.1 Hadamard Localization 365</p> <p>7.8.2 Sequential Multivolume Localization 366</p> <p>Exercises 368</p> <p>References370</p> <p><b>8 Spectral Editing and 2D NMR </b><b>375</b></p> <p>8.1 Introduction 375</p> <p>8.2 Quantitative Descriptions of NMR 375</p> <p>8.2.1 Density Matrix Formalism 376</p> <p>8.2.2 Classical Vector Model 377</p> <p>8.2.3 Correlated Vector Model 378</p> <p>8.2.4 Product Operator Formalism 379</p> <p>8.3 Scalar Evolution 380</p> <p>8.4 J‐Difference Editing 384</p> <p>8.4.1 Principle 384</p> <p>8.4.2 Practical Considerations 385</p> <p>8.4.3 GABA, 2HG, and Lactate 389</p> <p>8.5 Multiple Quantum Coherence Editing 395</p> <p>8.6 Spectral Editing Alternatives 400</p> <p>8.7 Heteronuclear Spectral Editing 402</p> <p>8.7.1 Proton‐observed, Carbon‐edited (POCE) MRS 402</p> <p>8.7.2 Polarization Transfer – INEPT and DEPT 407</p> <p>8.8 Broadband Decoupling 410</p> <p>8.9 Sensitivity 414</p> <p>8.10 Two‐dimensional NMR Spectroscopy 415</p> <p>8.10.1 Correlation Spectroscopy (COSY) 416</p> <p>8.10.2 J‐resolved Spectroscopy (JRES) 422</p> <p>8.10.3 In vivo 2D NMR Methods 424</p> <p>Exercises 429</p> <p>References 432</p> <p><b>9 Spectral Quantification </b><b>439</b></p> <p>9.1 Introduction 439</p> <p>9.2 Data Acquisition 440</p> <p>9.2.1 Magnetic Field Homogeneity 440</p> <p>9.2.2 Spatial Localization 442</p> <p>9.2.3 Water Suppression 442</p> <p>9.2.4 Sensitivity 442</p> <p>9.3 Data Preprocessing 443</p> <p>9.3.1 Phased‐array Coil Combination 443</p> <p>9.3.2 Phasing and Frequency Alignment 444</p> <p>9.3.3 Line‐shape Correction 444</p> <p>9.3.4 Removal of Residual Water 444</p> <p>9.3.5 Baseline Correction 446</p> <p>9.4 Data Quantification 447</p> <p>9.4.1 Time‐ and Frequency‐domain Parameters 447</p> <p>9.4.2 Prior Knowledge 450</p> <p>9.4.3 Spectral Fitting Algorithms 453</p> <p>9.4.4 Error Estimation 457</p> <p>9.5 Data Calibration 460</p> <p>9.5.1 Partial Saturation 461</p> <p>9.5.2 Nuclear Overhauser Effects 462</p> <p>9.5.3 Transverse Relaxation 462</p> <p>9.5.4 Diffusion 462</p> <p>9.5.5 Scalar Coupling 462</p> <p>9.5.6 Localization 463</p> <p>9.5.7 Frequency‐dependent Amplitude‐ and Phase Distortions 463</p> <p>9.5.8 NMR Visibility 463</p> <p>9.5.9 Internal Concentration Reference 464</p> <p>9.5.10 External Concentration Reference 466</p> <p>9.5.11 Phantom Replacement Concentration Reference 466</p> <p>Exercises 467</p> <p>References 469</p> <p><b>10 Hardware </b><b>473</b></p> <p>10.1 Introduction 473</p> <p>10.2 Magnets 473</p> <p>10.3 Magnetic Field Homogeneity 478</p> <p>10.3.1 Origins of Magnetic Field Inhomogeneity 478</p> <p>10.3.2 Effects of Magnetic Field Inhomogeneity 482</p> <p>10.3.3 Principles of Spherical Harmonic Shimming 485</p> <p>10.3.4 Practical Spherical Harmonic Shimming 489</p> <p>10.3.5 Alternative Shimming Strategies 491</p> <p>10.4 Magnetic Field Gradients 493</p> <p>10.4.1 Eddy Currents 498</p> <p>10.4.2 Preemphasis 499</p> <p>10.4.3 Active Shielding 503</p> <p>10.5 Radiofrequency (RF) Coils 503</p> <p>10.5.1 Electrical Circuit Analysis 503</p> <p>10.5.2 RF Coil Performance 509</p> <p>10.5.3 Spatial Field Properties 510</p> <p>10.5.3.1 Longitudinal Magnetic Fields 512</p> <p>10.5.3.2 Transverse Magnetic Fields 513</p> <p>10.5.4 Principle of Reciprocity 514</p> <p>10.5.4.1 Electromagnetic Wave Propagation 515</p> <p>10.5.5 Parallel Transmission 517</p> <p>10.5.6 RF Power and Specific Absorption Rate (SAR) 519</p> <p>10.5.7 Specialized RF Coils 520</p> <p>10.5.7.1 Combined Transmit and Receive RF Coils 521</p> <p>10.5.7.2 Phased‐Array Coils 522</p> <p>10.5.7.3 1H‐[13C] and 13C‐[1H] RF Coils 522</p> <p>10.5.7.4 Cooled and Superconducting RF Coils 525</p> <p>10.6 Complete MR System 526</p> <p>10.6.1 RF Transmission 526</p> <p>10.6.2 Signal Reception 527</p> <p>10.6.3 Quadrature Detection 528</p> <p>10.6.4 Dynamic Range 529</p> <p>10.6.5 Gradient and Shim Systems 530</p> <p>Exercises 531</p> <p>References 534</p> <p><b>Appendix A 541</b></p> <p>A.1 Matrix Calculations 541</p> <p>A.2 Trigonometric Equations 543</p> <p>A.3 Fourier Transformation 543</p> <p>A.3.1 Introduction 543</p> <p>A.3.2 Properties 544</p> <p>A.3.2.1 Linearity 544</p> <p>A.3.2.2 Time and Frequency Shifting 544</p> <p>A.3.2.3 Scaling 545</p> <p>A.3.2.4 Convolution 545</p> <p>A.3.3 Discrete Fourier Transformation 545</p> <p>A.4 Product Operator Formalism 546</p> <p>A.4.1 Cartesian Product Operators 546</p> <p>A.4.2 Shift (Lowering and Raising) Operators 548</p> <p>References 550</p> <p>Further Reading 551</p> <p>Index 553</p>
<p><b>Robin A. de Graaf, PhD,</b> is Professor at Yale University, School of Medicine, Department of Radiology and Biomedical Imaging, USA.
<p><b>Presents basic concepts, experimental methodology and data acquisition, and processing standards of</b> <b><i>in vivo</i></b><b> NMR spectroscopy</b> <p>This book covers, in detail, the technical and biophysical aspects of <i>in vivo</i> NMR techniques and includes novel developments in the field such as hyperpolarized NMR, dynamic <sup>13</sup>C NMR, automated shimming, and parallel acquisitions. Most of the techniques are described from an educational point of view, yet it still retains the practical aspects appreciated by experimental NMR spectroscopists. In addition, each chapter concludes with a number of exercises designed to review, and often extend, the presented NMR principles and techniques. <p>The third edition of <i>in vivo NMR Spectroscopy: Principles and Techniques</i> has been updated to include experimental detail on the developing area of hyperpolarization; a description of the semi-LASER sequence, which is now a method of choice; updated chemical shift data, including the addition of <sup>31</sup>P data; a troubleshooting section on common problems related to shimming, water suppression, and quantification; recent developments in data acquisition and processing standards; and MatLab scripts on the accompanying website to assist readers calculate radiofrequency pulses. <ul> <li>Provides an educational explanation and overview of <i>in vivo</i> NMR, while maintaining the practical aspects appreciated by experimental NMR spectroscopists</li> <li>Features more experimental methodology than previous editions</li> <li>End-of-chapter exercises that help drive home the principles and techniques and offer a more in-depth exploration of quantitative MR equations</li> <li>Designed to be used in conjunction with a teaching course on the subject</li> </ul> <p><i>in vivo NMR Spectroscopy: Principles and Techniques<sup>, </sup>3rd Edition</i> is aimed at all those involved in fundamental and/or diagnostic <i>in vivo</i> NMR, ranging from people working in dedicated <i>in vivo</i> NMR institutes, to radiologists in hospitals, researchers in high-resolution NMR and MRI, and in areas such as neurology, physiology, chemistry, and medical biology.

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