Differential phase contrast and dark field neutron imaging

Objective. X-ray phase contrast imaging is a promising technique for future clinical diagnostic as it can provide enhanced contrast in soft tissues compared to traditional x-ray attenuation-contrast imaging. However, the strict requirements on the x-ray coherence and the precise alignment of optical elements limit its applications towards clinical use. To solve this problem, mesh-based x-ray phase contrast imaging method with one hexagonal mesh is proposed for easy alignment and better image visualization. Approach. The mesh produces structured illuminations and the detector captures its distortions to reconstruct the absorption, differential phase contrast (DPC) and dark-field (DF) images of the sample. In this work, we fabricated a hexagonal mesh to simultaneously retrieve DPC and DF signals in three different directions with single shot. A phase retrieval algorithm to obtain artifacts-free phase from DPC images with three different directions is put forward and false color dark-field image is also reconstructed with tri-directional images. Mesh-shifting method based on this hexagonal mesh modulator is also proposed to reconstruct images with better image quality at the expense of increased dose. Main results. In numerical simulations, the proposed hexagonal mesh outperforms the traditional square mesh in image evaluation metrics performance and false color visualization with the same radiation dose. The experimental results demonstrate its feasiblity in real imaging systems and its advantages in quantitive imaging and better visualization. The proposed hexagonal mesh is easy to fabricate and can be successfully applied to x-ray source with it spot size up to 300 μm. Significance. This work opens new possibilities for quantitative x-ray non-destructive imaging and may also be instructive for research fields such as x-ray structured illumination microscopy (SIM), x-ray spectral imaging and x-ray phase contrast and dark-field computed tomography (CT).

In grating-based x-ray differential phase contrast (DPC) imaging, the measured signal amplitude of the phase shift induced by an image object is proportional to the so-called system sensitivity. Therefore, to achieve a better signal-to-noise (SNR) for improved imaging performance, it is generally believed that one should increase the system sensitivity by reducing the period of the analyzer grating or increasing the distance between the phase grating and analyzer grating. The purpose of this work is to theoretically and experimentally demonstrate that there is an optimal system sensitivity to attain the highest SNR for a given task provided that the standard phase-stepping acquisition and phase retrieval methods are used. When system sensitivity goes beyond this optimal value, SNR decreases and the imaging performance deteriorates. Due to the fundamental fact that the measured phase signal is a cyclic variable, the phase wrapping effect is inevitable in DPC imaging when the system sensitivity increases. The phase wrapping effect appears in both signal and noise measurements. The effect in the signal measurement is manifested in the so-called signal statistical bias and such effect often impacts the accuracy of the measurement. The phase wrapping effect also appears in the noise variance measurement and impacts the precision of the measurement. A thorough theoretical analysis was performed in this work to demonstrate the quantitative impacts of phase wrapping on both signal bias and noise variance and thus on the actual system SNR. The joint effect of phase wrapping in both the signal bias and noise variance yields an optimal system sensitivity to achieve the highest SNR. Both extensive numerical simulation studies and experimental studies were performed to validate the theoretical analysis. Both theoretical analysis and experimental studies show that the SNR of the DPC signal is not always proportional to the sensitivity due to the cyclic nature of the signal and the phase wrapping effect. For a given refraction angle and exposure level, there exists an optimal sensitivity factor that maximizes the SNR, beyond which, increasing the sensitivity will decrease the SNR. Increase of system sensitivity does not always improve x-ray DPC imaging performance provided that the standard phase-stepping acquisition and phase retrieval methods are used.

Purpose: The anatomical noise power spectra (NPS) for differential phase contrast (DPC) and dark field (DF) imaging have recently been characterized using a power-law model with two parameters, alpha and beta, an innovative extension to the methodology used in x-ray attenuation based breast imaging such as mammography, DBT, or cone-beam CT. Beta values of 3.6, 2.6, and 1.3 have been measured for absorption, DPC, and DF respectively for cadaver breasts imaged in the coronal plane; these dramatic differences should be reflected in their detection performance. The purpose of this study was to determine the impact of anatomical noise on breast calcification detection and compare the detection performance of the three contrast mechanisms of a multi-contrast x-ray imaging system. Methods: In our studies, a calcification image object was segmented out of the multi-contrast images of a cadaver breast specimen. 50 measured total NPS were measured from breast cadavers directly. The ideal model observer detectability was calculated for a range of doses (5–100%) and a range of calcification sizes (diameter = 0.25–2.5 mm). Results: Overall we found the highest average detectability corresponded to DPC imaging (7.4 for 1 mm calc.), with DF the next highest (3.8 for 1 mm calc.), and absorption the lowest (3.2 for 1 mm calc.). However, absorption imaging also showed the slowest dependence on dose of the three modalities due to the significant anatomical noise. DPC showed a peak detectability for calcifications ∼1.25 mm in diameter, DF showed a peak for calcifications around 0.75 mm in diameter, and absorption imaging had no such peak in the range explored. Conclusion: Understanding imaging performance for DPC and DF is critical to transition these modalities to the clinic. The results presented here offer new insight into how these modalities complement absorption imaging to maximize the likelihood of detecting early breast cancers. J. Garrett, Y. Ge, K. Li: Nothing to disclose. G.-H. Chen: Research funded, GE Healthcare; Research funded, Siemens AX.

DeepPhase: Learning phase contrast signal from dual energy X-ray absorption images

Optical diffraction tomography (ODT) is a promising label-free imaging method capable of quantitatively measuring the three-dimensional (3D) refractive index distribution of transparent samples. In recent years, partially coherent ODT (PC-ODT) has attracted increasing attention due to its system simplicity and absence of laser speckle noise. Quantitative phase imaging (QPI) technologies represented by Fourier ptychographic microscopy (FPM), differential phase contrast (DPC) imaging and intensity diffraction tomography (IDT) need to collect several or hundreds of intensity images, which usually introduce motion artifacts when shooting fast-moving targets, leading to a decrease in image quality. Hence, a quantitative real-time phase microscopy (qRPM) for extended depth of field (DOF) imaging based on 3D single-shot differential phase contrast (ssDPC) imaging method is proposed in this research study. qRPM incorporates a microlens array (MLA) to simultaneously collect spatial information and angular information. In subsequent optical information processing, a deconvolution method is used to obtain intensity stacks under different illumination angles in a raw light field image. Importing the obtained intensity stack into the 3D DPC imaging model is able to finally obtain the 3D refractive index distribution. The captured four-dimensional light field information enables the reconstruction of 3D information in a single snapshot and extending the DOF of qRPM. The imaging capability of the proposed qRPM system is experimental verified on different samples, achieve single-exposure 3D label-free imaging with an extended DOF for 160 µm which is nearly 30 times higher than the traditional microscope system.

The single-shot x-ray Talbot-Lau interferometer-based differential phase contrast (DPC) imaging is able to accelerate time-consuming data acquisition; however, the extracted phase image suffers from severe image artifacts. Here, we propose to estimate the DPC image via a deep convolutional neural network (CNN) incorporated with the physical imaging model. Instead of training the CNN with thousands of labeled data beforehand, both phantom and biological specimen validation experiments show that high-quality DPC images can be automatically generated from only one single-shot projection image with a certain periodic moiré pattern. This work provides a new, to the best of our knowledge, paradigm for single-shot x-ray DPC imaging.

The separation of diffraction effects from phase contrast is a major challenge for differential phase contrast (DPC) imaging in scanning transmission electron microscopy (STEM). The application of electron beam precession has previously been proven successful in homogenizing the direct beam and improving the imaging of both long-range electric and magnetic fields. However, magnetic STEM-DPC imaging performed in a low magnification (LM) STEM mode suffers from significant aberrations of the probe forming lens and the consequent impediment of small precession angles. By investigating the application of precession path segmentation to LM-STEM precessed scans for the imaging of LSMO and FeAl thin film samples, the initially reported benefits of precession were discovered to be less substantial than originally assumed. The segmentation methodology reveals that precession induced beam phase shifts account for a large part of the DPC induction profile smoothing, and the precession path is non-circular, leading to streaking artifacts in the reconstructed induction maps.

We describe a simple and fast technique to perform ultrasound differential phase contrast (DPC) imaging in arbitrarily thick scattering media. Although configured in a reflection geometry, DPC is based on transmission imaging and is a direct analog of optical differential interference contrast. DPC exploits the memory effect and works in combination with standard pulse-echo imaging, with no additional hardware or data requirements, enabling complementary phase contrast (in the transverse direction) without any need for intensive numerical computation. We experimentally demonstrate the principle of DPC using tissue phantoms with calibrated speed-of-sound inclusions.

Portal vein imaging is an important method for investigating portal venous disorders. However, the diagnostic requirements are not usually satisfied when using single imaging techniques. Diagnostic accuracy can be improved by combining different imaging techniques. Contrast agents that can be used for combined imaging modalities are needed. In this study, the feasibility of using microbubbles containing gadolinium (MCG) as contrast agents for both phase contrast imaging (PCI) and magnetic resonance imaging (MRI) are investigated. MCG were made by encapsulating sulfur hexafluoride (SF6) gas with gadolinium and lyophilized powder. Absorption contrast imaging (ACI) and PCI of MCG were performed and compared in vitro. MCG were injected into the main portal trunk of living rats. PCI and MRI were performed at 2 min and 10 min after MCG injection, respectively. PCI exploited the differences in the refractive index and visibly showed the MCG, which were not detectable by ACI. PCI could facilitate clear revelation of the MCG-infused portal veins. The diameter of the portal veins could be determined by the largest MCG in the same portal vein. The minimum diameter of clearly detected portal veins was about 300 µm by MRI. These results indicate that MCG could enhance both PCI and MRI for imaging portal veins. The detection sensitivity of PCI and MRI could compensate for each other when using MCG contrast agents for animals.

We introduce a lock-in method to increase the phase contrast in incoherent Differential Phase Contrast (DPC) imaging. The use of a smart pixel detector with in-pixel signal demodulation, paired with synchronized illumination, provides the basis of a bit-efficient approach to DPC. The experiments show an increased sensitivity by a factor of 8, for equivalent standard DPC measurements; single-shot sensitivity of 0.7 mrad at a frame rate of 1400 fps is demonstrated. This new approach may open the way for the use of incoherent phase microscopy in biological applications where extreme phase sensitivity and millisecond response time is required.

Grating-based interferometry/tomography is being rapidly developed for non-destructive evaluation of additive manufacturing test articles. An application requiring an efficient workflow is extremely necessary for stress and fatigue testing samples. At present, scientific workflows play an important role for computational experiments in additive manufacturing 3D printing and interferometry/tomography imaging analysis. A clear workflow template allows scientists to process experiments easier and faster. Work flow library grows, but to find an appropriate workflow for their task is challenging. In our research, there are mainly three portions in the workflow, interferometry analysis, image reconstruction and 3D visualization. Currently, the hierarchy of workflows in interferom etry/tomography projects is Mathematica, TomoPy/ASTRA/Jupyter notebook, VisTrails and Dragonfly. In general, two methods of interferometry analysis have been used in the first portion of workflow, single-shot interferometry and stepped-grating interferometry. As for the second portion, with a Jupyter notebook, the reconstruction method ’Gridrec’ in TomoPy and ’SIRT’ (Simultaneous Iterative Reconstruction Technique) in ASTRA gener ated a powerful reconstruction volume for absorption projections and dark-field projections separately. For the last portion, Dragonfly developed by ORS (Object Research System) company is a 3D visualization software with powerful scripting capabilities implemented in Python macros. Meanwhile, the VisTrails workflow incorporated both interferometry anal ysis and image reconstruction portions into VisTrails modules. Workflows in VisTrails hide much of the complexity of Mathematica or Python programming from users. Instead, with a simple GUI, it is possible for users to make their interferometry/tomography workflows through VisTrails modules. Especially, for DPC (differential phase contrast) images in grating-based interferome try/tomography, we addressed the phase unwrapping issue with the method of 2D integra tion through generating phase images. With the algorithm, we have demonstrated the 2D integrated phase images denote a clearer contrast than DPC images.

The application of two approaches for high‐throughput, high‐resolution X‐ray phase contrast tomographic imaging being used at the tomographic microscopy and coherent radiology experiments (TOMCAT) beamline of the SLS is discussed and illustrated. Differential phase contrast (DPC) imaging, using a grating interferometer and a phase‐stepping technique, is integrated into the beamline environment at TOMCAT in terms of the fast acquisition and reconstruction of data and the availability to scan samples within an aqueous environment. A second phase contrast method is a modified transfer of intensity approach that can yield the 3D distribution of the decrement of the refractive index of a weakly absorbing object from a single tomographic dataset. The two methods are complementary to one another: the DPC method is characterised by a higher sensitivity and by moderate resolution with larger samples; the modified transfer of intensity approach is particularly suited for small specimens when high resolution (around 1 µm) is required. Both are being applied to investigations in the biological and materials science fields.

Grating-based X-ray and neutron interferometry tomography using phase-stepping methods generates large data sets. An improved algorithm is presented for solving for the parameters to calculate transmissions, differential phase contrast, and dark-field images. The method takes advantage of the vectorization inherent in high-level languages such as Mathematica and MATLAB and can solve a 16 × 1k × 1k data set in less than a second. In addition, the algorithm can function with partial data sets. This is demonstrated with processing of a 16-step grating data set with partial use of the original data chosen without any restriction. Also, we have calculated the reduced chi-square for the fit and notice the effect of grating support structural elements upon the differential phase contrast image and have explored expanded basis set representations to mitigate the impact.

A new technique for obtaining confocal differential phase contrast is outlined. It is shown that this method involving a single pinhole and a split detector is easier to align and calibrate than the standard method of two pinholes and two detectors. Experimental calibration curves, which show that this arrangement does perform differential phase contrast imaging and that it can be used to measure surface height variations of the order of λ/600 per micrometer, are presented. Confocal scanning-beam reflection and transmission differential phase contrast images are presented.

Quantitative differential phase-contrast (DPC) imaging is one of the commonly used methods for phase retrieval. However, quantitative DPC imaging requires several pairwise intensity measurements, which makes it difficult to monitor living cells in real-time. In this study, we present a single-shot quantitative DPC imaging method based on the combination of deep learning (DL) and color-encoded illumination. Our goal is to train a model that can generate an isotropic quantitative phase image (i.e., target) directly from a single-shot intensity measurement (i.e., input). The target phase image was reconstructed using a linear-gradient pupil with two-axis measurements, and the model input was the measured color intensities obtained from a radially asymmetric color-encoded illumination pattern. The DL-based model was trained, validated, and tested using thirteen different cell lines. The total number of training, validation, and testing images was 264 (10 cells), 10 (1 cell), and 40 (2 cells), respectively. Our results show that the DL-based phase images are visually similar to the ground-truth phase images and have a high structural similarity index (>0.98). Moreover, the phase difference between the ground-truth and DL-based phase images was smaller than 13%. Our study shows the feasibility of using DL to generate quantitative phase imaging from a single-shot intensity measurement.