Marco Endrizzi

Low-dose phase contrast tomography with conventional x-ray sources

PURPOSE The edge illumination (EI) x-ray phase contrast imaging (XPCi) method has been recently further developed to perform tomographic and, thus, volumetric imaging. In this paper, the first tomographic EI XPCi images acquired with a conventional x-ray source at dose levels below that used for preclinical small animal imaging are presented. METHODS Two test objects, a biological sample and a custom-built phantom, were imaged with a laboratory-based EI XPCi setup in tomography mode. Tomographic maps that show the phase shift and attenuating properties of the object were reconstructed, and analyzed in terms of signal-to-noise ratio and quantitative accuracy. Dose measurements using thermoluminescence devices were performed. RESULTS The obtained images demonstrate that phase based imaging methods can provide superior results compared to attenuation based modalities for weakly attenuating samples also in 3D. Moreover, and, most importantly, they demonstrate the feasibility of low-dose imaging. In addition, the experimental results can be considered quantitative within the constraints imposed by polychromaticity. CONCLUSIONS The results, together with the methods dose efficiency and compatibility with conventional x-ray sources, indicate that tomographic EI XPCi can become an important tool for the routine imaging of biomedical samples.

Hard X-ray dark-field imaging with incoherent sample illumination

We report on a non-interferometric technique enabling dark-field imaging by using incoherent illumination and two achromatic optical elements. The simultaneous retrieval of absorption and differential phase images in the hard X-ray regime is also provided. We show that three projection images are sufficient to separate three signals: absorption, differential phase, and scattering. The method is highly efficient, also in terms of the dose delivered to the sample, flexible, robust against environmental vibrations, and scalable. It can be easily implemented in laboratories and translated into commercial systems, lending itself to a wide range of applications.

Sensitivity of laboratory based implementations of edge illumination X-ray phase-contrast imaging

We present a theoretical and experimental analysis of the angular sensitivity of edge illumination X-ray phase-contrast imaging in its implementation with conventional X-ray sources (sometimes referred to as the “coded-aperture” method). We study how the polychromaticity and finite source dimensions encountered in laboratory-based setups affect the detected signal. We also show that the sensitivity is independent of the period of the masks. Experimental images are presented and analyzed, proving that, despite the simple setup, high angular resolutions of a few hundred nanoradians can be obtained.

Visualization of small lesions in rat cartilage by means of laboratory-based x-ray phase contrast imaging

Being able to quantitatively assess articular cartilage in three-dimensions (3D) in small rodent animal models, with a simple laboratory set-up, would prove extremely important for the development of pre-clinical research focusing on cartilage pathologies such as osteoarthritis (OA). These models are becoming essential tools for the development of new drugs for OA, a disease affecting up to 1/3 of the population older than 50 years for which there is no cure except prosthetic surgery. However, due to limitations in imaging technology, high-throughput 3D structural imaging has not been achievable in small rodent models, thereby limiting their translational potential and their efficiency as research tools. We show that a simple laboratory system based on coded-aperture x-ray phase contrast imaging (CAXPCi) can correctly visualize the cartilage layer in slices of an excised rat tibia imaged both in air and in saline solution. Moreover, we show that small, surgically induced lesions are also correctly detected by the CAXPCi system, and we support this finding with histopathology examination. Following these successful proof-of-concept results in rat cartilage, we expect that an upgrade of the system to higher resolutions (currently underway) will enable extending the method to the imaging of mouse cartilage as well. From a technological standpoint, by showing the capability of the system to detect cartilage also in water, we demonstrate phase sensitivity comparable to other lab-based phase methods (e.g. grating interferometry). In conclusion, CAXPCi holds a strong potential for being adopted as a routine laboratory tool for non-destructive, high throughput assessment of 3D structural changes in murine articular cartilage, with a possible impact in the field similar to the revolution that conventional microCT brought into bone research.

Method for automatization of the alignment of a laboratory based x-ray phase contrast edge illumination system

Here we present a general alignment algorithm for an edge illumination x-ray phase contrast imaging system, which is used with the laboratory systems developed at UCL. It has the flexibility to be used with all current mask designs, and could also be applied to future synchrotron based systems. The algorithm has proved to be robust experimentally, and can be used for the automatization of future commercial systems through automatic alignment and alignment correction.

Quantitative evaluation of single-shot inline phase contrast imaging using an inverse compton x-ray source

Inverse compton scattering (ICS) x-ray sources are of current interest in biomedical imaging. We present an experimental demonstration of inline phase contrast imaging using a single picosecond pulse of the ICS source located at the BNL Accelerator Test Facility. The phase contrast effect is clearly observed. Its qualities are shown to be in agreement with the predictions of theoretical models through comparison of experimental and simulated images of a set of plastic wires of differing composition and size. Finally, we display an application of the technique to a biological sample, confirming the possibility of time-resolved imaging on the picosecond scale.

Theory and preliminary experimental verification of quantitative edge illumination x-ray phase contrast tomography

X-ray phase contrast imaging (XPCi) methods are sensitive to phase in addition to attenuation effects and, therefore, can achieve improved image contrast for weakly attenuating materials, such as often encountered in biomedical applications. Several XPCi methods exist, most of which have already been implemented in computed tomographic (CT) modality, thus allowing volumetric imaging. The Edge Illumination (EI) XPCi method had, until now, not been implemented as a CT modality. This article provides indications that quantitative 3D maps of an objects phase and attenuation can be reconstructed from EI XPCi measurements. Moreover, a theory for the reconstruction of combined phase and attenuation maps is presented. Both reconstruction strategies find applications in tissue characterisation and the identification of faint, weakly attenuating details. Experimental results for wires of known materials and for a biological object validate the theory and confirm the superiority of the phase over conventional, attenuation-based image contrast.

Absorption, refraction and scattering retrieval with an edge-illumination-based imaging setup

We have recently developed a new method based on edge-illumination for retrieving a three-image representation of the sample. A minimum of three intensity projections are required in order to retrieve the transmission, refraction and ultra-small-angle scattering properties of the sample. Here we show how the method can be adapted for particular cases in which some degree of a priori information about the sample might be available, limiting the number of required projections to two. Moreover, an iterative algorithm to correct for non-ideal optical elements is proposed and tested on numerical simulations, and finally validated on experimental data.

Single-image phase retrieval using an edge illumination X-ray phase-contrast imaging setup

A method enabling the retrieval of thickness or projected electron density of a sample from a single input image is derived theoretically and successfully demonstrated on experimental data.

Strategies for efficient and fast wave optics simulation of coded-aperture and other x-ray phase-contrast imaging methods

We derive a Fourier formulation of coded-aperture x-ray phase-contrast imaging, based on the wave theory of optics in the Fresnel approximation. We use this model to develop a flexible, efficient, and general simulation algorithm that can be easily adapted to other implementations of x-ray phase contrast imaging. Likewise, the algorithm enables a simple extension to 2D aperture designs, different acquisition schemes, etc. Problems related to numerical implementation of the algorithm are analyzed in detail, and simple rules are derived that enable us to avoid or at least mitigate them. Finally, comparisons with experimental data and data obtained with a different simulation algorithm are presented to validate the model and demonstrate its advantages in practical implementations. This also enabled us to demonstrate an increase in computational speed of more than one order of magnitude over a previous algorithm.