Literature DB >> 21386141

Imaging of nanoparticles with dual-energy computed tomography.

J L Ducote1, Y Alivov, S Molloi.   

Abstract

A simulation study was performed to determine the feasibility and performance of imaging nanoparticles as contrast agents in dual-energy computed tomography. An analytical simulation model was used to model the relevant signal-to-noise ratio (SNR) in dual-energy imaging for the specific case of a three-material patient phantom consisting of water, calcium hydroxyapatite and contrast agent. Elemental gold and iodine were both considered as contrast agents. Simulations were performed for a range of monoenergetic (20-150 keV) and polyenergetic (20-150 kVp) beam spectra. A reference configuration was defined with beam energies of 80 and 140 kVp to match current clinical practice. The effect of adding a silver filter to the high-energy beam was also studied. A figure of merit (FOM), which normalized the dual-energy SNR to the square root of the patient integral dose, was calculated for all cases. The units of the FOM were keV(-1/2). A simple Rose model of detectability was used to estimate the minimum concentration of either elements needed to be detected (SNR > 5). For monoenergetic beams, the peak FOM of gold was 6.4 × 10(-6) keV(-1/2), while the peak FOM of iodine was 3.1 × 10(-6) keV(-1/2), a factor of approximately 2 greater for gold. For polyenergetic spectra, at the reference energies of 80 and 140 kVp, the FOM for gold and iodine was 1.65 × 10(-6) and 5.0 × 10(-7) keV(-1/2), respectively, a factor of approximately 3.3 greater. Also at these energies, the minimum detectable concentration of gold was estimated to be 58.5 mg mL(-1), while iodine was estimated to be 117.5 mg mL(-1). The results suggest that the imaging of a gold nanoparticle contrast agent is well suited to current conditions used in clinical imaging. The addition of a silver filter of 800 µm further increased the image quality of the gold signal by approximately 50% for the same absorbed dose to the patient.

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Year:  2011        PMID: 21386141      PMCID: PMC3153953          DOI: 10.1088/0031-9155/56/7/008

Source DB:  PubMed          Journal:  Phys Med Biol        ISSN: 0031-9155            Impact factor:   3.609


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