Details

Biomedical Imaging


Biomedical Imaging

Principles and Applications
1. Aufl.

von: Reiner Salzer

120,99 €

Verlag: Wiley
Format: PDF
Veröffentl.: 09.04.2012
ISBN/EAN: 9781118271902
Sprache: englisch
Anzahl Seiten: 448

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Beschreibungen

This book presents and describes imaging technologies that can be used to study chemical processes and structural interactions in dynamic systems, principally in biomedical systems. The imaging technologies, largely biomedical imaging technologies such as MRT, Fluorescence mapping, raman mapping, nanoESCA, and CARS microscopy, have been selected according to their application range and to the chemical information content of their data. These technologies allow for the analysis and evaluation of delicate biological samples, which must not be disturbed during the profess. Ultimately, this may mean fewer animal lab tests and clinical trials.
<p>Preface xv</p> <p>Contributors xvii</p> <p><b>1 Evaluation of Spectroscopic Images 1<br /></b><i>Patrick</i> <i>W.T.</i> <i>Krooshof,</i> <i>Geert</i> <i>J.</i> <i>Postma,</i> <i>Willem</i> <i>J.</i> <i>Melssen,</i> <i>and</i> <i>Lutgarde</i> <i>M.C.</i> <i>Buydens</i></p> <p>1.1 Introduction 1</p> <p>1.2 Data Analysis 2</p> <p>1.2.1 Similarity Measures 3</p> <p>1.2.2 Unsupervised Pattern Recognition 4</p> <p>1.2.2.1 Partitional Clustering 4</p> <p>1.2.2.2 Hierarchical Clustering 6</p> <p>1.2.2.3 Density-Based Clustering 7</p> <p>1.2.3 Supervised Pattern Recognition 9</p> <p>1.2.3.1 Probability of Class Membership 9</p> <p>1.3 Applications 11</p> <p>1.3.1 Brain Tumor Diagnosis 11</p> <p>1.3.2 MRS Data Processing 12</p> <p>1.3.2.1 Removing MRS Artifacts 12</p> <p>1.3.2.2 MRS Data Quantitation 13</p> <p>1.3.3 MRI Data Processing 14</p> <p>1.3.3.1 Image Registration 15</p> <p>1.3.4 Combining MRI and MRS Data 16</p> <p>1.3.4.1 Reference Data Set 16</p> <p>1.3.5 Probability of Class Memberships 17</p> <p>1.3.6 Class Membership of Individual Voxels 18</p> <p>1.3.7 Classification of Individual Voxels 20</p> <p>1.3.8 Clustering into Segments 22</p> <p>1.3.9 Classification of Segments 23</p> <p>1.3.10 Future Directions 24</p> <p>References 25</p> <p><b>2 Evaluation of Tomographic Data 30<br /></b><i>Jorg</i> <i>van</i> <i>den</i> <i>Hoff</i></p> <p>2.1 Introduction 30</p> <p>2.2 Image Reconstruction 33</p> <p>2.3 Image Data Representation: Pixel Size and Image Resolution 34</p> <p>2.4 Consequences of Limited Spatial Resolution 39</p> <p>2.5 Tomographic Data Evaluation: Tasks 46</p> <p>2.5.1 Software Tools 46</p> <p>2.5.2 Data Access 47</p> <p>2.5.3 Image Processing 47</p> <p>2.5.3.1 Slice Averaging 48</p> <p>2.5.3.2 Image Smoothing 48</p> <p>2.5.3.3 Coregistration and Resampling 51</p> <p>2.5.4 Visualization 52</p> <p>2.5.4.1 Maximum Intensity Projection (MIP) 52</p> <p>2.5.4.2 Volume Rendering and Segmentation 54</p> <p>2.5.5 Dynamic Tomographic Data 56</p> <p>2.5.5.1 Parametric Imaging 57</p> <p>2.5.5.2 Compartment Modeling of Tomographic Data 57</p> <p>2.6 Summary 61</p> <p>References 61</p> <p><b>3 X-Ray Imaging 63<br /></b><i>Volker</i> <i>Hietschold</i></p> <p>3.1 Basics 63</p> <p>3.1.1 History 63</p> <p>3.1.2 Basic Physics 64</p> <p>3.2 Instrumentation 66</p> <p>3.2.1 Components 66</p> <p>3.2.1.1 Beam Generation 66</p> <p>3.2.1.2 Reduction of Scattered Radiation 67</p> <p>3.2.1.3 Image Detection 69</p> <p>3.3 Clinical Applications 76</p> <p>3.3.1 Diagnostic Devices 76</p> <p>3.3.1.1 Projection Radiography 76</p> <p>3.3.1.2 Mammography 78</p> <p>3.3.1.3 Fluoroscopy 81</p> <p>3.3.1.4 Angiography 82</p> <p>3.3.1.5 Portable Devices 84</p> <p>3.3.2 High Voltage and Image Quality 85</p> <p>3.3.3 Tomography/Tomosynthesis 87</p> <p>3.3.4 Dual Energy Imaging 87</p> <p>3.3.5 Computer Applications 88</p> <p>3.3.6 Interventional Radiology 92</p> <p>3.4 Radiation Exposure to Patients and Employees 92</p> <p>References 95</p> <p><b>4 Computed Tomography 97<br /></b><i>Stefan</i> <i>Ulzheimer</i> <i>and</i> <i>Thomas</i> <i>Flohr</i></p> <p>4.1 Basics 97</p> <p>4.1.1 History 97</p> <p>4.1.2 Basic Physics and Image Reconstruction 100</p> <p>4.2 Instrumentation 102</p> <p>4.2.1 Gantry 102</p> <p>4.2.2 X-ray Tube and Generator 103</p> <p>4.2.3 MDCT Detector Design and Slice Collimation 103</p> <p>4.2.4 Data Rates and Data Transmission 107</p> <p>4.2.5 Dual Source CT 107</p> <p>4.3 Measurement Techniques 109</p> <p>4.3.1 MDCT Sequential (Axial) Scanning 109</p> <p>4.3.2 MDCT Spiral (Helical) Scanning 109</p> <p>4.3.2.1 Pitch 110</p> <p>4.3.2.2 Collimated and Effective Slice Width 110</p> <p>4.3.2.3 Multislice Linear Interpolation and z-Filtering 111</p> <p>4.3.2.4 Three-Dimensional Backprojection and Adaptive Multiple Plane Reconstruction (AMPR) 114</p> <p>4.3.2.5 Double z-Sampling 114</p> <p>4.3.3 ECG-Triggered and ECG-Gated Cardiovascular CT 115</p> <p>4.3.3.1 Principles of ECG-Triggering and ECG-Gating 115</p> <p>4.3.3.2 ECG-Gated Single-Segment and Multisegment Reconstruction 118</p> <p>4.4 Applications 119</p> <p>4.4.1 Clinical Applications of Computed Tomography 119</p> <p>4.4.2 Radiation Dose in Typical Clinical Applications and Methods for Dose Reduction 122</p> <p>4.5 Outlook 125</p> <p>References 127</p> <p><b>5 Magnetic Resonance Technology 131<br /></b><i>Boguslaw</i> <i>Tomanek</i> <i>and</i> <i>Jonathan</i> <i>C.</i> <i>Sharp</i></p> <p>5.1 Introduction 131</p> <p>5.2 Magnetic Nuclei Spin in a Magnetic Field 133</p> <p>5.2.1 A Pulsed rf Field Resonates with Magnetized Nuclei 135</p> <p>5.2.2 The MR Signal 137</p> <p>5.2.3 Spin Interactions Have Characteristic Relaxation Times 138</p> <p>5.3 Image Creation 139</p> <p>5.3.1 Slice Selection 139</p> <p>5.3.2 The Signal Comes Back—The Spin Echo 142</p> <p>5.3.3 Gradient Echo 143</p> <p>5.4 Image Reconstruction 145</p> <p>5.4.1 Sequence Parameters 146</p> <p>5.5 Image Resolution 148</p> <p>5.6 Noise in the Image—SNR 149</p> <p>5.7 Image Weighting and Pulse Sequence Parameters TE and TR 150</p> <p>5.7.1 <i>T</i><sub>2</sub>-Weighted Imaging 150</p> <p>5.7.2 <i>T</i><sup>∗</sup><sub>2</sub> -Weighted Imaging 151</p> <p>5.7.3 Proton-Density-Weighted Imaging 152</p> <p>5.7.4 <i>T</i><sub>1</sub>-Weighted Imaging 152</p> <p>5.8 A Menagerie of Pulse Sequences 152</p> <p>5.8.1 EPI 154</p> <p>5.8.2 FSE 154</p> <p>5.8.3 Inversion-Recovery 155</p> <p>5.8.4 DWI 156</p> <p>5.8.5 MRA 158</p> <p>5.8.6 Perfusion 159</p> <p>5.9 Enhanced Diagnostic Capabilities of MRI—Contrast Agents 159</p> <p>5.10 Molecular MRI 159</p> <p>5.11 Reading the Mind—Functional MRI 160</p> <p>5.12 Magnetic Resonance Spectroscopy 161</p> <p>5.12.1 Single Voxel Spectroscopy 163</p> <p>5.12.2 Spectroscopic Imaging 163</p> <p>5.13 MR Hardware 164</p> <p>5.13.1 Magnets 164</p> <p>5.13.2 Shimming 167</p> <p>5.13.3 Rf Shielding 168</p> <p>5.13.4 Gradient System 168</p> <p>5.13.5 MR Electronics—The Console 169</p> <p>5.13.6 Rf Coils 170</p> <p>5.14 MRI Safety 171</p> <p>5.14.1 Magnet Safety 171</p> <p>5.14.2 Gradient Safety 173</p> <p>5.15 Imaging Artefacts in MRI 173</p> <p>5.15.1 High Field Effects 174</p> <p>5.16 Advanced MR Technology and Its Possible Future 175</p> <p>References 175</p> <p><b>6 Toward A 3D View of Cellular Architecture: Correlative Light Microscopy and Electron Tomography 180<br /></b><i>Jack</i> <i>A.</i> <i>Valentijn,</i> <i>Linda</i> <i>F.</i> <i>van</i> <i>Driel,</i> <i>Karen</i> <i>A.</i> <i>Jansen,</i> <i>Karine</i> <i>M.</i> <i>Valentijn,</i> <i>and</i> <i>Abraham</i> <i>J.</i> <i>Koster</i></p> <p>6.1 Introduction 180</p> <p>6.2 Historical Perspective 181</p> <p>6.3 Stains for CLEM 182</p> <p>6.4 Probes for CLEM 183</p> <p>6.4.1 Probes to Detect Exogenous Proteins 183</p> <p>6.4.1.1 Green Fluorescent Protein 183</p> <p>6.4.1.2 Tetracysteine Tags 186</p> <p>6.4.1.3 Theme Variations: Split GFP and GFP-4C 187</p> <p>6.4.2 Probes to Detect Endogenous Proteins 188</p> <p>6.4.2.1 Antifluorochrome Antibodies 189</p> <p>6.4.2.2 Combined Fluorescent and Gold Probes 189</p> <p>6.4.2.3 Quantum Dots 190</p> <p>6.4.2.4 Dendrimers 191</p> <p>6.4.3 Probes to Detect Nonproteinaceous Molecules 192</p> <p>6.5 CLEM Applications 193</p> <p>6.5.1 Diagnostic Electron Microscopy 193</p> <p>6.5.2 Ultrastructural Neuroanatomy 194</p> <p>6.5.3 Live-Cell Imaging 196</p> <p>6.5.4 Electron Tomography 197</p> <p>6.5.5 Cryoelectron Microscopy 198</p> <p>6.5.6 Immuno Electron Microscopy 201</p> <p>6.6 Future Perspective 202</p> <p>References 205</p> <p><b>7 Tracer Imaging 215<br /></b><i>Rainer</i> <i>Hinz</i></p> <p>7.1 Introduction 215</p> <p>7.2 Instrumentation 216</p> <p>7.2.1 Radioisotope Production 216</p> <p>7.2.2 Radiochemistry and Radiopharmacy 219</p> <p>7.2.3 Imaging Devices 220</p> <p>7.2.4 Peripheral Detectors and Bioanalysis 225</p> <p>7.3 Measurement Techniques 228</p> <p>7.3.1 Tomographic Image Reconstruction 228</p> <p>7.3.2 Quantification Methods 229</p> <p>7.3.2.1 The Flow Model 230</p> <p>7.3.2.2 The Irreversible Model for Deoxyglucose 230</p> <p>7.3.2.3 The Neuroreceptor Binding Model 233</p> <p>7.4 Applications 234</p> <p>7.4.1 Neuroscience 234</p> <p>7.4.1.1 Cerebral Blood Flow 234</p> <p>7.4.1.2 Neurotransmitter Systems 235</p> <p>7.4.1.3 Metabolic and Other Processes 238</p> <p>7.4.2 Cardiology 240</p> <p>7.4.3 Oncology 240</p> <p>7.4.3.1 Angiogenesis 240</p> <p>7.4.3.2 Proliferation 241</p> <p>7.4.3.3 Hypoxia 241</p> <p>7.4.3.4 Apoptosis 242</p> <p>7.4.3.5 Receptor Imaging 242</p> <p>7.4.3.6 Imaging Gene Therapy 243</p> <p>7.4.4 Molecular Imaging for Research in Drug Development 243</p> <p>7.4.5 Small Animal Imaging 244</p> <p>References 244</p> <p><b>8 Fluorescence Imaging 248<br /></b><i>Nikolaos</i> <i>C.</i> <i>Deliolanis,</i> <i>Christian</i> <i>P.</i> <i>Schultz,</i> <i>and</i> <i>Vasilis</i> <i>Ntziachristos</i></p> <p>8.1 Introduction 248</p> <p>8.2 Contrast Mechanisms 249</p> <p>8.2.1 Endogenous Contrast 249</p> <p>8.2.2 Exogenous Contrast 251</p> <p>8.3 Direct Methods: Fluorescent Probes 251</p> <p>8.4 Indirect Methods: Fluorescent Proteins 252</p> <p>8.5 Microscopy 253</p> <p>8.5.1 Optical Microscopy 253</p> <p>8.5.2 Fluorescence Microscopy 254</p> <p>8.6 Macroscopic Imaging/Tomography 260</p> <p>8.7 Planar Imaging 260</p> <p>8.8 Tomography 262</p> <p>8.8.1 Diffuse Optical Tomography 266</p> <p>8.8.2 Fluorescence Tomography 266</p> <p>8.9 Conclusion 267</p> <p>References 268</p> <p><b>9 Infrared and Raman Spectroscopic Imaging 275<br /></b><i>Gerald</i> <i>Steiner</i></p> <p>9.1 Introduction 275</p> <p>9.2 Instrumentation 278</p> <p>9.2.1 Infrared Imaging 278</p> <p>9.2.2 Near-Infrared Imaging 281</p> <p>9.3 Raman Imaging 282</p> <p>9.4 Sampling Techniques 283</p> <p>9.5 Data Analysis and Image Evaluation 285</p> <p>9.5.1 Data Preprocessing 287</p> <p>9.5.2 Feature Selection 287</p> <p>9.5.3 Spectral Classification 288</p> <p>9.5.4 Image Processing Including Pattern Recognition 292</p> <p>9.6 Applications 292</p> <p>9.6.1 Single Cells 292</p> <p>9.6.2 Tissue Sections 292</p> <p>9.6.2.1 Brain Tissue 294</p> <p>9.6.2.2 Skin Tissue 295</p> <p>9.6.2.3 Breast Tissue 298</p> <p>9.6.2.4 Bone Tissue 299</p> <p>9.6.3 Diagnosis of Hemodynamics 300</p> <p>References 301</p> <p><b>10 Coherent Anti-Stokes Raman Scattering Microscopy 304<br /></b><i>Annika</i> <i>Enejder,</i> <i>Christoph</i> <i>Heinrich,</i> <i>Christian</i> <i>Brackmann,</i> <i>Stefan</i> <i>Bernet,</i> <i>and</i> <i>Monika</i> <i>Ritsch-Marte</i></p> <p>10.1 Basics 304</p> <p>10.1.1 Introduction 304</p> <p>10.2 Theory 306</p> <p>10.3 CARS Microscopy in Practice 309</p> <p>10.4 Instrumentation 310</p> <p>10.5 Laser Sources 311</p> <p>10.6 Data Acquisition 314</p> <p>10.7 Measurement Techniques 316</p> <p>10.7.1 Excitation Geometry 316</p> <p>10.7.2 Detection Geometry 318</p> <p>10.7.3 Time-Resolved Detection 319</p> <p>10.7.4 Phase-Sensitive Detection 319</p> <p>10.7.5 Amplitude-Modulated Detection 320</p> <p>10.8 Applications 320</p> <p>10.8.1 Imaging of Biological Membranes 321</p> <p>10.8.2 Studies of Functional Nutrients 321</p> <p>10.8.3 Lipid Dynamics and Metabolism in Living Cells and Organisms 322</p> <p>10.8.4 Cell Hydrodynamics 324</p> <p>10.8.5 Tumor Cells 325</p> <p>10.8.6 Tissue Imaging 325</p> <p>10.8.7 Imaging of Proteins and DNA 326</p> <p>10.9 Conclusions 326</p> <p>References 327</p> <p><b>11 Biomedical Sonography 331<br /></b><i>Georg</i> <i>Schmitz</i></p> <p>11.1 Basic Principles 331</p> <p>11.1.1 Introduction 331</p> <p>11.1.2 Ultrasonic Wave Propagation in Biological Tissues 332</p> <p>11.1.3 Diffraction and Radiation of Sound 333</p> <p>11.1.4 Acoustic Scattering 337</p> <p>11.1.5 Acoustic Losses 338</p> <p>11.1.6 Doppler Effect 339</p> <p>11.1.7 Nonlinear Wave Propagation 339</p> <p>11.1.8 Biological Effects of Ultrasound 340</p> <p>11.1.8.1 Thermal Effects 340</p> <p>11.1.8.2 Cavitation Effects 340</p> <p>11.2 Instrumentation of Real-Time Ultrasound Imaging 341</p> <p>11.2.1 Pulse-Echo Imaging Principle 341</p> <p>11.2.2 Ultrasonic Transducers 342</p> <p>11.2.3 Beamforming 344</p> <p>11.2.3.1 Beamforming Electronics 344</p> <p>11.2.3.2 Array Beamforming 345</p> <p>11.3 Measurement Techniques of Real-Time Ultrasound Imaging 347</p> <p>11.3.1 Doppler Measurement Techniques 347</p> <p>11.3.1.1 Continuous Wave Doppler 347</p> <p>11.3.1.2 Pulsed Wave Doppler 349</p> <p>11.3.1.3 Color Doppler Imaging and Power Doppler Imaging 351</p> <p>11.3.2 Ultrasound Contrast Agents and Nonlinear Imaging 353</p> <p>11.3.2.1 Ultrasound Contrast Media 353</p> <p>11.3.2.2 Harmonic Imaging Techniques 356</p> <p>11.3.2.3 Perfusion Imaging Techniques 357</p> <p>11.3.2.4 Targeted Imaging 358</p> <p>11.4 Application Examples of Biomedical Sonography 359</p> <p>11.4.1 B-Mode, M-Mode, and 3D Imaging 359</p> <p>11.4.2 Flow and Perfusion Imaging 362</p> <p>References 365</p> <p><b>12 Acoustic Microscopy for Biomedical Applications 368<br /></b><i>Jurgen</i> <i>Bereiter-Hahn</i></p> <p>12.1 Sound Waves and Basics of Acoustic Microscopy 368</p> <p>12.1.1 Propagation of Sound Waves 369</p> <p>12.1.2 Main Applications of Acoustic Microscopy 371</p> <p>12.1.3 Parameters to Be Determined and General Introduction into Microscopy with Ultrasound 371</p> <p>12.2 Types of Acoustic Microscopy 372</p> <p>12.2.1 Scanning Laser Acoustic Microscope (LSAM) 373</p> <p>12.2.2 Pulse-Echo Mode: Reflection-Based Acoustic Microscopy 373</p> <p>12.2.2.1 Reflected Amplitude Measurements 379</p> <p>12.2.2.2 V(z) Imaging 380</p> <p>12.2.2.3 V(f) Imaging 382</p> <p>12.2.2.4 Interference-Fringe-Based Image Analysis 383</p> <p>12.2.2.5 Determination of Phase and the Complex Amplitude 386</p> <p>12.2.2.6 Combining <i>V</i> <i>(f)</i> with Reflected Amplitude and Phase Imaging 386</p> <p>12.2.2.7 Time-Resolved SAM and Full Signal Analysis 388</p> <p>12.3 Biomedical Applications of Acoustic Microscopy 391</p> <p>12.3.1 Influence of Fixation on Acoustic Parameters of Cells and Tissues 391</p> <p>12.3.2 Acoustic Microscopy of Cells in Culture 392</p> <p>12.3.3 Technical Requirements 393</p> <p>12.3.3.1 Mechanical Stability 393</p> <p>12.3.3.2 Frequency 393</p> <p>12.3.3.3 Coupling Fluid 393</p> <p>12.3.3.4 Time of Image Acquisition 394</p> <p>12.3.4 What Is Revealed by SAM: Interpretation of SAM Images 394</p> <p>12.3.4.1 Sound Velocity, Elasticity, and the Cytoskeleton 395</p> <p>12.3.4.2 Attenuation 400</p> <p>12.3.4.3 Viewing Subcellular Structures 401</p> <p>12.3.5 Conclusions 401</p> <p>12.4 Examples of Tissue Investigations using SAM 403</p> <p>12.4.1 Hard Tissues 404</p> <p>12.4.2 Cardiovascular Tissues 405</p> <p>12.4.3 Other Soft Tissues 406</p> <p>References 406</p>
<p>“This would be highly beneficial to scientists and engineers seeking careers in biomedical imaging.”  (<i>Journal<br /> of Biomedical Optics</i>, 1 December 2012) </p> <p>“The text is expertly integrated with high-quality figures and includes an index. This book is suitable for researchers and engineers in a variety of disciplines. I highly recommend it as a comprehensive introduction to nanofabrication techniques.”  (<i>Optics & Photonics News</i>, 1 October 2012)</p>
<p><b>REINER SALZER, PHD,</b> is a professor at the Institute for Analytical Chemistry at Technische Universität in Dresden, Germany.
<p><b>A WALK THROUGH THE EXCITING FIELD OF MULTIMODALITY IMAGING AND ITS CLINICAL APPLICATIONS</b> <p>This book offers a unique approach to biomedical imaging. Unlike other books on the market that cover just one or several modalities, <i>Biomedical Imaging: Principles and Applications</i> describes all important biomedical imaging modalities, showing how to capitalize on their combined strengths when investigating processes and interactions in dynamic systems. <p>Geared to non-experts looking for quick guidance on what modalities to choose for their work without getting bogged down in technical details, the book discusses technical fundamentals, molecular background, evaluation procedures, and case studies of clinical applications. With an emphasis on technologies known for their application range and the chemical information content of their data, the book covers such established modalities as X-ray, CT, MRI, and tracer imaging, as well as technologies using light or sound, including fluorescence and Raman imaging, CARS microscopy, sonography, and acoustic microscopy. <p>Including more than 200 figures (many in color) to help clarify the text, <i>Biomedical Imaging</i>: <ul> <li>Reviews the current state of image-based diagnostic medicine as well as methods and tools for visualization</li> <li>Covers for each modality the basics of how it works, information parameters, instrumentation, and applications</li> <li>Compares the strengths and weaknesses of different imaging technologies</li> <li>Focuses on current and emerging applications for chemical analysis in extremely delicate samples</li> <li>Explains the utility of multimodality imaging in the rapidly expanding field of biophotonics</li> </ul> <p>An excellent startup guide for researchers and clinicians wishing to combine different imaging technologies for a true multimodality approach to problem solving, <i>Biomedical Imaging</i> is also a useful reference for engineers who need to understand the biomedical basis of the measured data.

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