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A sparse array offers a significant reduction in the complexity of ultrasonic imaging systems by decreasing the number of active elements and associated electrical circuits needed to form a focused beam. Consequently, for 1-D arrays, it has been adopted in the development of miniaturized systems such as portable, handheld, or smartphone-based systems. Previously, we developed an analytic method that can design a pair of 1-D periodic sparse arrays (PSAs) satisfying three specific constraints, which are the array size, desired grating lobe level, and sparseness factor (SF). In this study, we further developed our method by incorporating aperture weighting functions, which take the form of tapered rectangular functions to introduce null points on the beam pattern. These null points effectively suppress grating lobes generated by a matching pair of arrays. The design process commences with determining transmit and receive PSA patterns, followed by deriving corresponding aperture weighting functions. First, aperture functions of a base and weighting arrays are convolved, which is then upsampled to the targeted array size. Finally, the upsampled aperture is convolved to an aperture function of a subarray, resulting in weighted PSAs (wPSAs). Pulsed wave (PW) simulation confirmed improved grating lobe suppression with wPSAs compared to PSAs. Phantom imaging experiments using a 1-D phased array validated the enhanced contrast due to suppressed grating lobes but at the cost of small degradation in lateral resolution. The signal-to-noise ratio (SNR) also gradually declined with the greater SFs, but no significant difference in SNR was observed between wPSAs and PSAs. Finally, in vivo echocardiography imaging highlighted the clinical potential of wPSAs, particularly with high SFs. Overall, these results suggest that wPSAs can effectively enhance contrast compared to PSAs under the given SF or, alternatively, wPSA with greater SFs can achieve comparable image quality to PSAs with lower SFs. In conclusion, the wPSA approach holds promise for further reducing the complexity of ultrasound imaging systems.

Implementation of a high-frequency ultrasound (HFUS) beamformer is computationally challenging because of its high sampling rate. This article introduces an efficient beamformer with sub-Nyquist sampling (or bandpass sampling) that is suitable for HFUS imaging. Our approach used channel radio frequency data sampled at bandpass sampling rate (i.e., 4/ 3f c ) and postfiltering-based interpolation to reduce the computational complexity. A polyphase structure for interpolation was used to further reduce the computational burden while maintaining an adequate delay resolution ( δ ). The performance of the proposed beamformer (i.e., 4/ 3f c sampling with sixfold interpolation, δ = 8f c ) was compared with that of the conventional method (i.e., 4f c sampling with fourfold interpolation, δ = 16f c ). Ultrafast coherent compounding imaging was used in simulation, in vitro and in vivo imaging experiments. Axial/lateral resolution and contrast-to-noise ratio (CNR) values were measured for quantitative evaluation. The number of transmit pulse cycles was varied from 1 to 3 using two transducers with different fractional bandwidths (67% and 98%). In the simulation, the proposed and conventional methods showed the similar -6-dB axial beam widths (63.5 and 61.5 μm , respectively) from the two-cycle transmit pulse using the transducer with a bandwidth of 67%. In vitro and in vivo imaging experiments were performed using a Verasonics ultrasound research platform equipped with a high-frequency array transducer (20-46 MHz). The in vitro imaging results using a wire target showed consistent results with the simulation study (i.e., disparity at -6-dB axial resolution). The in vivo feasibility study with a murine mouse model with breast cancer was also performed, and the proposed method yielded a similar image quality compared with the conventional method. From these studies, it was demonstrated that the proposed HFUS beamformer based on the bandpass sampling can substantially reduce the computational complexity while minimizing the loss of spatial resolution for HFUS imaging.

Ultrasound imaging using a matrix array allows real-time multi-planar volumetric imaging. To enhance image quality, the matrix array should provide fast volumetric ultrasound imaging with spatially consistent focusing in the lateral and elevational directions. However, because of the significantly increased data size, dealing with massive and continuous data acquisition is a significant challenge. We have designed an imaging acquisition sequence that handles volumetric data efficiently using a single 256-channel Verasonics ultrasound research platform multiplexed with a 1024-element matrix array. The developed sequence has been applied for building an ultrasonic pupilometer. Our results demonstrate the capability of the developed approach for structural visualization of an ex vivo porcine eye and the temporal response of the modeled eye pupil with moving iris at the volume rate of 30 Hz. Our study provides a fundamental ground for researchers to establish their own volumetric ultrasound imaging platform and could stimulate the development of new volumetric ultrasound approaches and applications.

This paper introduces a configurable combined laser, ultrasound, and elasticity (CLUE) imaging platform. The CLUE platform enables imaging sequences capable of simultaneously providing quantitative acoustic, optical, and mechanical contrast for comprehensive diagnosis and monitoring of complex diseases, such as cancer. The CLUE imaging platform was developed on a Verasonics ultrasound scanner integrated with a pulsed laser, and it was designed to be modular and scalable to allow researchers to create their own specific imaging sequences efficiently. The CLUE imaging platform and sequence were demonstrated in a tissue-mimicking phantom containing a stiff inclusion labeled with optically-activated nanodroplets and in an ex vivo mouse spleen. We have shown that CLUE imaging can simultaneously capture multi-functional imaging signals providing quantitative information on tissue.

Phase-change perfluorohexane nanodroplets (PFHnDs) are a new class of recondensable submicrometer-sized contrast agents that have potential for contrast-enhanced and super-resolution ultrasound imaging with an ability to reach extravascular targets. The PFHnDs can be optically triggered to undergo vaporization, resulting in spatially stationary, temporally transient microbubbles. The vaporized PFHnDs are hyperechoic in ultrasound imaging for several to hundreds of milliseconds before recondensing to their native, hypoechoic, liquid nanodroplet state. The decay of echogenicity, i.e., the dynamic behavior of the ultrasound signal from optically triggered PFHnDs in ultrasound imaging, can be captured using high-frame-rate ultrasound imaging. We explore the possibility to manipulate the echogenicity dynamics of optically triggered PFHnDs in ultrasound imaging by changing the phase of the ultrasound imaging pulse. Specifically, the ultrasound imaging system was programmed to transmit two imaging pulses with inverse polarities. We show that the imaging pulse phase can affect the amplitude and the temporal behavior of PFHnD echogenicity in ultrasound imaging. The results of this study demonstrate that the ultrasound echogenicity is significantly increased (about 78% improvement) and the hyperechoic timespan of optically triggered PFHnDs is significantly longer (about four times) if the nanodroplets are imaged by an ultrasound pulse starting with rarefactional pressure versus a pulse starting with compressional pressure. Our finding has direct and significant implications for contrast-enhanced ultrasound imaging of droplets in applications such as super-resolution imaging and molecular imaging where detection of individual or low-concentration PFHnDs is required.

Objective: The purpose of this study was to introduce combined multiwavelength photoacoustic (PA) and plane-wave ultrasound (US) imaging referred to as mwPA/pwUS imaging capable of probing the rapid dynamic behavior of optically activated phase-change contrast agents., Methods: A dedicated mwPA/pwUS imaging sequence was developed based on a programmable US system synchronized with a tunable laser to irradiate tissue with laser pulses at desired optical wavelengths and to acquire post laser pulse PA images followed by ultrafast plane-wave US images. To evaluate the mwPA/pwUS imaging, a capillary filled with optically responsive perfluorohexane nanodroplets (PFHnDs) containing a dye with the peak absorption at 760 nm was imaged with optical wavelengths ranging from 700 to 940 nm. The differences between post-laser ultrafast US images [i.e., differential US (ΔUS)] were taken to visualize the recondensation dynamics of PFHnDs at each wavelength., Results: The PA images of PFHnDs showed higher contrast near 760 nm wavelength, corresponding to the peak absorption of the dye encapsulated in the PFHnDs. Moreover, the ΔUS signals immediately after 760-nm pulsed laser irradiation were also high due to the increased US contrast associated with vaporized PFHnDs., Conclusion: The mwPA/pwUS imaging allowed for the US-based optical spectroscopic characterization of PFHnDs and their dynamics., Significance: The introduced mwPA/pwUS imaging sequence can be used in various clinical applications where both spectroscopic PA imaging of endogenous and/or exogenous chromophores and ultrafast US imaging of phase-change nanodroplets are desired.

Super-resolution imaging with moving microbubbles has shown potential in identifying fine details of deep-lying vascular compartments. To image the extravascular targets, this paper has employed nanometer-sized, optically triggered perfluorohexane nanodroplets (PFHnDs). In response to pulsed laser irradiation, the PFHnDs repeatedly vaporize and stochastically recondense, resulting in random changes of ultrasound signals. Our previous study has shown that the stochastic recondensation of the PFHnDs can be used to isolate individual PFHnDs for super-resolution imaging. This paper introduces an improved method for super-resolution imaging with ultrafast ultrasound imaging of PFHnDs. The previous method was based on subtraction of two consecutive ultrasound images to detect signals from recondensed, isolated droplets, whereas our current method compounds respective multiple pre- and post-recondensation ultrafast ultrasound images prior to subtraction to improve the spatial resolution further. To evaluate the axial and lateral resolutions of our method, we repeatedly imaged a phantom containing PFHnDs using a programmable ultrasound system synchronized with a pulsed laser system. As a result, our method improved the lateral and axial resolutions by 54% and 68%, respectively, over the previous super-resolution imaging approach, indicating that it can be used for localizing extravascular molecular targets with superior accuracy.

Shear-wave elasticity imaging (SWEI) enables the quantitative assessment of the mechanical properties of tissue. In SWEI, the effective generation of acoustic radiation force is of paramount importance. Consequently, several research groups have investigated various transmit beamforming and pulse-sequencing methods. To further improve the efficiency of the shear-wave generation, and therefore, to increase the quality of SWEI, we introduce a technique referred to as "multiangle compound SWEI" (MAC-SWEI), which uses simultaneous multiangular push beams created by dual-phase transmit focusing. By applying a constant phase offset on every other element of an array transducer, dual-phase transmit focusing creates both main and grating lobes (i.e., multiangular push beams for pushing) to simultaneously generate shear waves with several wavefront angles. The shear waves propagating at different angles are separated by multidirectional filtering in the frequency domain, leading to the reconstruction of multiple spatially co-registered shear-wave velocity maps. To form a single-elasticity image, these maps are combined, while regions associated with known artifacts created by the push beams are omitted. Overall, we developed and tested the MAC-SWEI method using Field II quantitative simulations and the experiments performed using a programmable ultrasound imaging system. Our results suggest that MAC-SWEI with dual-phase transmit focusing may improve the quality of elasticity maps.