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S. Mattsson / Medical Physics in the Baltic States 7 (2009) 6 - 10<br />

of a single-tube x-ray or by the necessity of rapid tube<br />

current adaptation [5].<br />

Imaging of a given material mixture using dual-source<br />

CT is performed with two X-ray beams of different<br />

effective photon energies. The combined absorption<br />

spectrum of the mixture is sampled at two points of the<br />

energy spectrum. These two data points, together with<br />

a priori knowledge of the mixture’s components and<br />

their relative densities, can be used to determine the<br />

concentration of three materials in each voxel<br />

examined.<br />

CT with flat panel detectors<br />

Large-area flat panel detectors are now more and more<br />

used as an alternative to the conventional CT [6].<br />

Examples of use are 1) routine interventional and<br />

intraoperative imaging using C-arm-based<br />

interventional flat panel detector CT e.g in connection<br />

with brachytherapy, 2) CT image-guided external<br />

tumor therapy, which is one of the fastest growing<br />

applications. Attaching a standard X-ray tube and a flat<br />

panel detector to a rotating linear accelerator allows for<br />

CT imaging of the patient on the therapy couch. The<br />

system is capable of producing images of soft tissue<br />

with good spatial resolution at acceptable imaging<br />

doses [7]. 3) CT for dedicated maxillo-facial scanning<br />

[8] and 4) CT for dedicated imaging of the breast. Last,<br />

but not least, 5) flat panel detector technology has also<br />

been used in standard CTs [9, 10].<br />

The development of the flat panel detector technology<br />

has stimulated much of the developments and research<br />

in 3D imaging. Micro-CT also receives increasing<br />

attention due the interest in molecular and small-animal<br />

imaging.<br />

In external beam radiotherapy, the use of the treatment<br />

beam for imaging is of high interest because this<br />

application requires no additional hardware and the<br />

image obtained gives an exact image of the treatment.<br />

Such imaging has been possible thanks to the<br />

development of electronic portal imaging devices<br />

(EPID). Megavoltage cone beam computed<br />

tomography can be used for treatment planning in 3D<br />

conformal radiotherapy and IMRT, adaptive radiation<br />

therapy, single fraction palliative treatment and for the<br />

treatment of patients with metal prostheses.<br />

2.2.2. Tomosynthesis<br />

Tomosynthesis is a form of limited angle tomography<br />

that produces “slice” images from a series of projection<br />

images acquired as the X-ray tube moves over a<br />

prescribed angular range, typically from – 25 degrees<br />

to + 25 degrees in relation to the angle for the ordinary<br />

projection image. Because the projection images are<br />

not acquired over a full 360° rotation around the<br />

patient, the resolution in the z direction i.e., in the<br />

depth direction perpendicular to the x-y plane of the<br />

projection images is limited. However, the spatial<br />

8<br />

resolution in the x-y plane of the reconstructed slices is<br />

often superior to CT, and the ease of use in conjunction<br />

with conventional radiography makes tomosynthesis a<br />

potentially quite useful imaging modality [11].<br />

3. Molecular imaging<br />

Nuclear medicine or molecular imaging is based on an<br />

i.v. injection, oral administration or inhalation of a<br />

radioactive tracer. Upon administration one awaits<br />

distribution and accumulation of the tracer in the<br />

region of interest, e.g. an organ or a tumour. The<br />

emitted radiation is mapped by a collimator (planar<br />

nuclear medicine and SPECT) or coincidence using<br />

two detectors (PET), 2D or 3D, iterative reconstruction<br />

or filtered back projection, and attenuation correction.<br />

Focus in imaging has changed from structures to a<br />

combination of structures and functions, creating a<br />

renewed interest for nuclear medicine methods, which<br />

can visualise physiologic functions and metabolism in<br />

the human body and also have a potential for molecular<br />

imaging. This will be of high importance for the<br />

advancement of molecular medicine [12], drug<br />

development and delivery techniques [13].<br />

3.1. Planar nuclear medicine<br />

The basic measurement instrument in nuclear medicine<br />

is still the gamma cameras using a NaI(Tl) scintillator<br />

block coupled to an array of photomultiplier tubes. In<br />

recent years there has been a growing interest in<br />

developing compact gamma cameras to improve<br />

nuclear medicine imaging. These are of three types:<br />

1. One or more scintillation crystals coupled to a<br />

single position-sensitive photomultiplier tube<br />

2. A position-sensitive solid-state detector<br />

3. An array of scintillation crystals coupled to an<br />

array of solid-state photo detectors.<br />

Type 1 cameras are expensive, have significant dead<br />

area, and have geometric distortion and non-uniform<br />

gain that can vary with both time and count rate. Type<br />

2 cameras have been under development for over 20<br />

years. The best candidate for room temperature<br />

operation is CdZnTe, a high-atomic-number, solid-state<br />

crystal. However CdZnTe tends to be expensive and is<br />

difficult to manufacture in volumes large enough to<br />

form arrays of useful imaging size. Type 3 cameras<br />

typically use silicon photodiode arrays.<br />

3.2. SPECT<br />

Conventional nuclear medicine images compress the 3dimensional<br />

(3D) distributions of radiotracers into a 2dimensional<br />

image. Tomographic images remove these<br />

difficulties but at the price of longer acquisition times,<br />

poorer spatial resolution, and the susceptibility to<br />

artefacts. Recent advances in SPECT instrumentation

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