Current diagnosis of prostate cancer relies on histological analysis of tissue samples acquired by biopsy, which could benefit from real-time identification of suspicious lesions. Photoacoustic tomography has the potential to provide real-time targets for prostate biopsy guidance with chemical selectivity, but light delivered from the rectal cavity has been unable to penetrate to the anterior prostate. To overcome this barrier, a urethral device with cylindrical illumination is developed for whole-prostate imaging, and its performance as a function of angular light coupling is evaluated with a prostate-mimicking phantom.

Microwaves, which have a ∼10-cm wavelength, can penetrate deeper into tissue than photons, heralding exciting deep tissue applications such as modulation or imaging via the thermoacoustic effect. Thermoacoustic conversion efficiency is however very low, even with an exogenous contrast agent. We break this low-conversion limit, using a split ring resonator to effectively collect and confine the microwaves into a submillimeter hot spot for ultrasound emission and achieve a conversion efficiency over 2000 times higher than other reported thermoacoustic contrast agents. Importantly, the frequency of emitted ultrasound can be precisely tuned and multiplexed by modulation of the microwave pulses. Such performance is inaccessible by a piezoelectric-based transducer or a photoacoustic emitter and, therefore, split ring resonators open up new opportunities to study the frequency response of cells in ultrasonic biomodulation. For applications in deep tissue localization, a split ring resonator can be used as a wireless, battery-free ultrasound beacon placed under a breast phantom.

No abstract