X-ray microtomography

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3D rendering of a µCT scan of a leaf piece, resolution circa 40 µm/voxel.

X-ray microtomography, like tomography and x-ray computed tomography, uses x-rays to create cross-sections of a physical object that can be used to recreate a virtual model (3D model) without destroying the original model. The prefix micro- (symbol: µ) is used to indicate that the pixel sizes of the cross-sections are in the micrometre range.[1] These pixel sizes have also resulted in the terms high-resolution x-ray tomography, micro–computed tomography (micro-CT or µCT), and similar terms. Sometimes the terms high-resolution CT (HRCT) and micro-CT are differentiated,[2] but in other cases the term high-resolution micro-CT is used.[3] Virtually all tomography today is computed tomography.

Micro-CT has applications both in medical imaging and in industrial computed tomography. In general, there are two types of scanner setups. In one setup, the X-ray source and detector are typically stationary during the scan while the sample/animal rotates. The second setup, much more like a clinical CT scanner, is gantry based where the animal/specimen is stationary in space while the X-ray tube and detector rotate around. These scanners are typically used for small animals (in vivo scanners), biomedical samples, foods, microfossils, and other studies for which minute detail is desired.

The first X-ray microtomography system was conceived and built by Jim Elliott in the early 1980s. The first published X-ray microtomographic images were reconstructed slices of a small tropical snail, with pixel size about 50 micrometers.[4]

Working principle[edit]

Imaging system[edit]

Fan beam reconstruction[edit]

The fan-beam system is based on a one-dimensional (1D) X-ray detector and an electronic X-ray source, creating 2D cross-sections of the object. Typically used in human computed tomography systems.

Cone beam reconstruction[edit]

The cone-beam system is based on a 2D X-ray detector (camera) and an electronic X-ray source, creating projection images that later will be used to reconstruct the image cross-sections.

Open/Closed systems[edit]

Open X-ray system[edit]

In an open system, X-rays may escape or leak out, thus the operator must stay behind a shield, have special protective clothing, or operate the scanner from a distance or a different room. Typical examples of these scanners are the human versions, or designed for big objects.

Closed X-ray system[edit]

In a closed system, X-ray shielding is put around the scanner so the operator can put the scanner on a desk or special table. Although the scanner is shielded, care must be taken and the operator usually carries a dose meter, since X-rays have a tendency to be absorbed by metal and then re-emitted like an antenna. Although a typical scanner will produce a relatively harmless volume of X-rays, repeated scannings in a short timeframe could pose a danger.

Closed systems tend to become very heavy because lead is used to shield the X-rays. Therefore, the smaller scanners only have a small space for samples.

3D image reconstruction[edit]

The principle[edit]

Because microtomography scanners offer isotropic, or near isotropic, resolution, display of images does not need to be restricted to the conventional axial images. Instead, it is possible for a software program to build a volume by 'stacking' the individual slices one on top of the other. The program may then display the volume in an alternative manner.

Volume rendering[edit]

Volume rendering is a technique used to display a 2D projection of a 3D discretely sampled data set, as produced by a microtomography scanner. Usually these are acquired in a regular pattern (e.g., one slice every millimeter) and usually have a regular number of image pixels in a regular pattern. This is an example of a regular volumetric grid, with each volume element, or voxel represented by a single value that is obtained by sampling the immediate area surrounding the voxel.

Image segmentation[edit]

Where different structures have similar threshold density, it can become impossible to separate them simply by adjusting volume rendering parameters. The solution is called segmentation, a manual or automatic procedure that can remove the unwanted structures from the image.

Typical use[edit]

Biomedical[edit]

  • Both in vitro and in vivo small animal imaging
  • Human skin samples
  • Bone samples, ranging in size from rodents to human biopsies
  • Lung imaging using respiratory gating
  • Cardiovascular imaging using cardiac gating
  • Tumor imaging (may require contrast agents)
  • Soft tissue imaging[5]
  • Insects[6]

Electronics[edit]

  • Small electronic components. E.g. DRAM IC in plastic case.

Microdevices[edit]

Composite materials and metallic foams[edit]

Polymers, plastics[edit]

Diamonds[edit]

  • Detecting defects in a diamond and finding the best way to cut it.

Food and seeds[edit]

Wood and paper[edit]

Building materials[edit]

Geology[edit]

Microfossils[edit]

  • Bentonic foraminifers

Space[edit]

Stereo images[edit]

  • Visualizing with blue and green or blue filters to see depth

Others[edit]

References[edit]

  1. ^ X-Ray Microtomography at the US National Library of Medicine Medical Subject Headings (MeSH)
  2. ^ Dame Carroll JR, Chandra A, Jones AS, Berend N, Magnussen JS, King GG (2006-07-26), "Airway dimensions measured from micro-computed tomography and high-resolution computed tomography", Eur Respir J 28 (4): 712–720, PMID 16870669. 
  3. ^ Duan J, Hu C, Chen H (2013-01-07), "High-resolution micro-CT for morphologic and quantitative assessment of the sinusoid in human cavernous hemangioma of the liver", PLOS ONE 8 (1): e53507, doi:10.1371/journal.pone.0053507, PMID 23308240. 
  4. ^ Elliott, J. C.; Dover, S. D. (1982). "X-ray microtomography". Journal of Microscopy 126 (2): 211. doi:10.1111/j.1365-2818.1982.tb00376.x. 
  5. ^ Mizutani, R; Suzuki, Y (2012). "X-ray microtomography in biology". Micron (Oxford, England : 1993) 43 (2–3): 104–15. doi:10.1016/j.micron.2011.10.002. PMID 22036251. 
  6. ^ Van De Kamp, T.; Vagovic, P.; Baumbach, T.; Riedel, A. (2011). "A Biological Screw in a Beetle's Leg". Science 333 (6038): 52. doi:10.1126/science.1204245. PMID 21719669. 
  7. ^ Gerard van Dalen, Han Blonk, Henrie van Aalst, Cris Luengo Hendriks 3-D Imaging of Foods Using X-Ray Microtomography. G.I.T. Imaging & Microscopy (March 2003), pp. 18–21
  8. ^ Jurewicz, A. J. G.; Jones, S. M.; Tsapin, A.; Mih, D. T.; Connolly, H. C., Jr.; Graham, G. A. (2003). "Locating Stardust-like Particles in Aerogel Using X-Ray Techniques". Lunar and Planetary Science. XXXIV. 
  9. ^ Tsuchiyama, A.; Uesugi, M.; Matsushima, T.; Michikami, T.; Kadono, T.; Nakamura, T.; Uesugi, K.; Nakano, T.; Sandford, S. A. (2011). "Three-Dimensional Structure of Hayabusa Samples: Origin and Evolution of Itokawa Regolith". Science 333 (6046): 1125–8. doi:10.1126/science.1207807. PMID 21868671. 

External links[edit]