ABSTRACT
The thermoacoustic (TA) contrast mechanism relies on rapid tissue heating and subsequent thermal expansion. TA computerized tomography (TCT) is therefore inverse source imaging. The TA contrast mechanism provides information complementary to that revealed by current diagnostic imaging techniques, but has been limited to just a few centimeters depth penetration. In this article, whole organ TCT is demonstrated on a large swine kidney. TA sinograms show that TA signal generated by high-power, very high frequency (VHF) electromagnetic pulses is detectable after travel through 6 cm of soft tissue. Reconstructed images provide resolution sufficient to track progression of calyces throughout the kidney. Because VHF electromagnetic energy can easily penetrate the abdomen of large adults, our results indicate that whole organ TA imaging is feasible in vivo, provided an ultrasound array can be placed near the region of interest. Pulses of 22 to 25 kW with carrier frequency 108 MHz and 900 ns pulse width were applied at a 100-Hz pulse repetition frequency to generate a 13-kV/m electric field and TA signal. Only 2 to 5 mJ was absorbed in the kidney per pulse, causing temperature and pressure jumps of only 5e-6°C and 4 Pa averaged throughout the 141-g specimen. TA pulses were detected by focused, single-element transducers (V306, Panametrics), amplified by 54 dB and averaged 64 times to reduce electronic noise. Data were measured over a cylindrical measurement aperture of radius 5 cm and length 6 cm, by rotating the specimen 1.8 degrees between tomographic views and translating 2 mm between slices. Reconstruction via filtered backprojection yields in-plane resolution better than 5 mm, but suffers significant blurring between planes. Both in-plane resolution and slice sensitivity profile could be improved by applying shorter irradiation pulsewidths and using less directional transducers. Both hardware changes would be recommended for a clinical prototype.
