Single-side access, isotropic resolution and multispectral 3D photoacoustic imaging with rotate-translate scanning of ultrasonic detector array

TL;DR

This paper presents a novel rotate-translate scanning method for 3D photoacoustic imaging that achieves near-isotropic resolution and multispectral capabilities using a single-side access ultrasound array.

Contribution

Introduction of a rotate-translate scanning scheme that significantly improves resolution and image quality in 3D photoacoustic imaging with a planar detector array.

Findings

Achieved ~170 μm isotropic resolution over 8.5 mm cube.

Demonstrated multispectral imaging with ultrafast wavelength shifting.

Validated the approach in vitro for potential in vivo applications.

Abstract

Photoacoustic imaging can achieve high-resolution three-dimensional visualization of optical absorbers at penetration depths ~ 1 cm in biological tissues by detecting optically-induced high ultrasound frequencies. Tomographic acquisition with ultrasound linear arrays offers an easy implementation of single-side access, parallelized and high-frequency detection, but usually comes with an image quality impaired by the directionality of the detectors. Indeed, a simple translation of the array perpendicularly to its median imaging plane is often used, but results both in a poor resolution in the translation direction and in strong limited view artifacts. To improve the spatial resolution and the visibility of complex structures while keeping a planar detection geometry, we introduce, in this paper, a novel rotate-translate scanning scheme, and investigate the performance of a scanner implemented at 15 MHz center frequency. The developed system achieved a quasi-isotropic uniform 3D resolution of ~170 um over a cubic volume of side length 8.5 mm, i.e. an improvement in the resolution in the translation direction by almost one order of magnitude. Dual wavelength imaging was also demonstrated with ultrafast wavelength shifting. The validity of our approach was shown in vitro. We discuss the ability to enable in vivo imaging for preclinical and clinical studies.