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      From Corrosion Casting to Virtual Dissection: Contrast‐Enhanced Vascular Imaging using Hafnium Oxide Nanocrystals

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          Abstract

          Vascular corrosion casting is a method used to visualize the three dimensional (3D) anatomy and branching pattern of blood vessels. A polymer resin is injected in the vascular system and, after curing, the surrounding tissue is removed. The latter often deforms or even fractures the fragile cast. Here, a method is proposed that does not require corrosion, and is based on in situ micro computed tomography (micro‐CT) scans. To overcome the lack of CT contrast between the polymer cast and the animals' surrounding soft tissue, hafnium oxide nanocrystals (HfO 2 NCs) are introduced as CT contrast agents into the resin. The NCs dramatically improve the overall CT contrast of the cast and allow for straightforward segmentation in the CT scans. Careful design of the NC surface chemistry ensures the colloidal stability of the NCs in the casting resin. Using only 5 m% of HfO 2 NCs, high‐quality cardiovascular casts of both zebrafish and mice can be automatically segmented using CT imaging software. This allows to differentiate even m‐scale details without having to alter the current resin injection methods. This new method of virtual dissection by visualizing casts in situ using contrast‐enhanced CT imaging greatly expands the application potential of the technique.

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          Angiotensin II promotes atherosclerotic lesions and aneurysms in apolipoprotein E-deficient mice.

          Increased plasma concentrations of angiotension II (Ang II) have been implicated in atherogenesis. To examine this relationship directly, we infused Ang II or vehicle for 1 month via osmotic minipumps into mature apoE(-/-) mice. These doses of Ang II did not alter arterial blood pressure, body weight, serum cholesterol concentrations, or distribution of lipoprotein cholesterol. However, Ang II infusions promoted an increased severity of aortic atherosclerotic lesions. These Ang II-induced lesions were predominantly lipid-laden macrophages and lymphocytes; moreover, Ang II promoted a marked increase in the number of macrophages present in the adventitial tissue underlying lesions. Unexpectedly, pronounced abdominal aortic aneurysms were present in apoE(-/-) mice infused with Ang II. Sequential sectioning of aneurysmal abdominal aorta revealed two major characteristics: an intact artery that is surrounded by a large remodeled adventitia, and a medial break with pronounced dilation and more modestly remodeled adventitial tissue. Although no atherosclerotic lesions were visible at the medial break point, the presence of hyperlipidemia was required because infusions of Ang II into apoE(+/+) mice failed to generate aneurysms. These results demonstrate that increased plasma concentrations of Ang II have profound and rapid effects on vascular pathology when combined with hyperlipidemia, in the absence of hemodynamic influences.
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            Simultaneous phase and amplitude extraction from a single defocused image of a homogeneous object.

            We demonstrate simultaneous phase and amplitude extraction from a single defocused image of a homogeneous object. Subject to the assumptions explicitly stated in the derivation, the algorithm solves the twin-image problem of in-line holography and is capable of analysing data obtained using X-ray microscopy, electron microscopy, neutron microscopy or visible-light microscopy, especially as they relate to defocus and point projection methods. Our simple, robust, non-iterative and computationally efficient method is applied to data obtained using an X-ray phase contrast ultramicroscope.
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              Surface modification of inorganic nanoparticles for development of organic–inorganic nanocomposites—A review

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Small Methods
                Small Methods
                Wiley
                2366-9608
                2366-9608
                January 10 2024
                Affiliations
                [1 ] Department of Chemistry Ghent University Ghent 9000 Belgium
                [2 ] Department of Chemistry University of Basel Basel 4058 Switzerland
                [3 ] Department of Biomolecular Medicine Ghent University Ghent 9000 Belgium
                [4 ] Center for X‐ray Tomography Ghent University Ghent 9000 Belgium
                [5 ] Laboratory of Veterinary Morphology Ghent University Merelbeke 9820 Belgium
                [6 ] Centre for Polymer Material Technologies Ghent University Ghent 9052 Belgium
                [7 ] Laboratory for Chemical Technology Ghent University Ghent 9052 Belgium
                [8 ] Swiss Light Source Paul Scherrer Institut Villigen PSI 5232 Switzerland
                [9 ] Swiss Nanoscience Institute University of Basel Basel 4056 Switzerland
                [10 ] Institute of Biomedical Engineering and Technology Ghent University Ghent 9000 Belgium
                Article
                10.1002/smtd.202301499
                0ee230de-1b93-48ee-8f21-058dbb730a9d
                © 2024

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