27,934 research outputs found
Ultrasound localization microscopy to image and assess microvasculature in a rat kidney.
The recent development of ultrasound localization microscopy, where individual microbubbles (contrast agents) are detected and tracked within the vasculature, provides new opportunities for imaging the vasculature of entire organs with a spatial resolution below the diffraction limit. In stationary tissue, recent studies have demonstrated a theoretical resolution on the order of microns. In this work, single microbubbles were localized in vivo in a rat kidney using a dedicated high frame rate imaging sequence. Organ motion was tracked by assuming rigid motion (translation and rotation) and appropriate correction was applied. In contrast to previous work, coherence-based non-linear phase inversion processing was used to reject tissue echoes while maintaining echoes from very slowly moving microbubbles. Blood velocity in the small vessels was estimated by tracking microbubbles, demonstrating the potential of this technique to improve vascular characterization. Previous optical studies of microbubbles in vessels of approximately 20 microns have shown that expansion is constrained, suggesting that microbubble echoes would be difficult to detect in such regions. We therefore utilized the echoes from individual MBs as microscopic sensors of slow flow associated with such vessels and demonstrate that highly correlated, wideband echoes are detected from individual microbubbles in vessels with flow rates below 2âmm/s
Exploiting flow dynamics for super-resolution in contrast-enhanced ultrasound
Ultrasound localization microscopy offers new radiation-free diagnostic tools
for vascular imaging deep within the tissue. Sequential localization of echoes
returned from inert microbubbles with low-concentration within the bloodstream
reveal the vasculature with capillary resolution. Despite its high spatial
resolution, low microbubble concentrations dictate the acquisition of tens of
thousands of images, over the course of several seconds to tens of seconds, to
produce a single super-resolved image. %since each echo is required to be well
separated from adjacent microbubbles. Such long acquisition times and stringent
constraints on microbubble concentration are undesirable in many clinical
scenarios. To address these restrictions, sparsity-based approaches have
recently been developed. These methods reduce the total acquisition time
dramatically, while maintaining good spatial resolution in settings with
considerable microbubble overlap. %Yet, non of the reported methods exploit the
fact that microbubbles actually flow within the bloodstream. % to improve
recovery. Here, we further improve sparsity-based super-resolution ultrasound
imaging by exploiting the inherent flow of microbubbles and utilize their
motion kinematics. While doing so, we also provide quantitative measurements of
microbubble velocities. Our method relies on simultaneous tracking and
super-localization of individual microbubbles in a frame-by-frame manner, and
as such, may be suitable for real-time implementation. We demonstrate the
effectiveness of the proposed approach on both simulations and {\it in-vivo}
contrast enhanced human prostate scans, acquired with a clinically approved
scanner.Comment: 11 pages, 9 figure
Complementarity of PALM and SOFI for super-resolution live cell imaging of focal adhesions
Live cell imaging of focal adhesions requires a sufficiently high temporal
resolution, which remains a challenging task for super-resolution microscopy.
We have addressed this important issue by combining photo-activated
localization microscopy (PALM) with super-resolution optical fluctuation
imaging (SOFI). Using simulations and fixed cell focal adhesion images, we
investigated the complementarity between PALM and SOFI in terms of spatial and
temporal resolution. This PALM-SOFI framework was used to image focal adhesions
in living cells, while obtaining a temporal resolution below 10 s. We
visualized the dynamics of focal adhesions, and revealed local mean velocities
around 190 nm per minute. The complementarity of PALM and SOFI was assessed in
detail with a methodology that integrates a quantitative resolution and
signal-to-noise metric. This PALM and SOFI concept provides an enlarged
quantitative imaging framework, allowing unprecedented functional exploration
of focal adhesions through the estimation of molecular parameters such as the
fluorophore density and the photo-activation and photo-switching rates
On using gait to enhance frontal face extraction
Visual surveillance finds increasing deployment formonitoring urban environments. Operators need to be able to determine identity from surveillance images and often use face recognition for this purpose. In surveillance environments, it is necessary to handle pose variation of the human head, low frame rate, and low resolution input images. We describe the first use of gait to enable face acquisition and recognition, by analysis of 3-D head motion and gait trajectory, with super-resolution analysis. We use region- and distance-based refinement of head pose estimation. We develop a direct mapping to relate the 2-D image with a 3-D model. In gait trajectory analysis, we model the looming effect so as to obtain the correct face region. Based on head position and the gait trajectory, we can reconstruct high-quality frontal face images which are demonstrated to be suitable for face recognition. The contributions of this research include the construction of a 3-D model for pose estimation from planar imagery and the first use of gait information to enhance the face extraction process allowing for deployment in surveillance scenario
- âŠ