Ultrasound imaging is a wide spread technique used in medical imaging as well as in non-destructive testing. The technique offers many advantages such as real-time imaging, good resolution, prompt acquisition, ease of use, and low cost compared to other techniques such as x-ray imaging. However, the maximum frame rate achievable is limited as several beams must be emitted to compute a single image. For each emitted beam, one must wait for the wave to propagate back and forth, thus imposing a limit to the frame rate. Several attempts have been made to use less beams while maintaining image quality. Although efficiently increasing the frame rate, these techniques still use several transmit beams. Compressive Sensing (CS), a universal data completion scheme based on convex optimization, has been successfully applied to a number of imaging modalities over the past few years. Using a priori knowledge of the signal, it can compute an image using less data allowing for shorter acquisition times. In this paper, it is shown that a valid CS framework can be derived from ultrasound propagation theory, and that this framework can be used to compute images of scatterers using only one plane wave as a transmit beam.
Abstract. We present an integrated photoacoustic and ultrasonic three-dimensional (3-D) volumetric imaging system based on a two-dimensional (2-D) matrix array ultrasound probe. A wavelength-tunable dye laser pumped by a Q-switched Nd:YAG laser serves as the light source and a modified commercial ultrasound imaging system (iU22, Philips Healthcare) with a 2-D array transducer (X7-2, Philips Healthcare) detects both the pulse-echo ultrasound and photoacoustic signals. A multichannel data acquisition system acquires the RF channel data. The imaging system enables rendering of co-registered 3-D ultrasound and photoacoustic images without mechanical scanning. The resolution along the azimuth, elevation, and axial direction are measured to be 0.69, 0.90 and 0.84 mm for photoacoustic imaging. In vivo 3-D photoacoustic mapping of the sentinel lymph node was demonstrated in a rat model using methylene blue dye. These results highlight the clinical potential of 3-D PA imaging for identification of sentinel lymph nodes for cancer staging in humans.
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