Tomographic imaging started with clinical X-ray computed tomography (CT) in 1972 (Hounsfield 1973). Since then, CT technology has rapidly advanced and clinical CT became radiology’s powerhouse. In addition to clinical CT imaging, there is increasing need for preclinical exams such as scans of tissue samples, organs or whole animals (in vitro or in vivo) that are used as models to evaluate human diseases and therapies (IEEE 2004). For example, noninvasive imaging of mice gains in importance due to recent advances in mouse genomics and the production of transgenic mouse models. Longitudinal studies that use a single animal population can provide internally consistent long-term data and help to reduce the number of animals used and to cut down the costs.
This chapter will further be restricted to those widely used scanners that employ an area detector and therefore acquire the data in cone-beam geometry. Neither former generations of micro-CT scanners that use only a single detector row or even a single detector element nor scanners based on cyclotron radiation that require expensive electron accelerators and therefore are hardly available will be discussed here.
Basic CT principles are discussed at first. Then, we will detail today’s micro-CT design followed by considerations about image noise, spatial resolution and dose. To become aware of potential pitfalls, the chapter finishes with discussing sources of image artifacts. Besides one image showing nondestructive material testing, our focus lies in small animal imaging and imaging of tissue samples.
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Kachelrieß, M. (2008). Micro-CT. In: Semmler, W., Schwaiger, M. (eds) Molecular Imaging I. Handbook of Experimental Pharmacology, vol 185/1. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-72718-7_2
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