60 research outputs found
High resolution micro arthrography of hard and soft tissues in a murine model
SummaryObjectiveRecent developments on high resolution micro computed tomography (μCT) allow imaging of soft tissues in small animal joints. Nevertheless, μCT images cannot distinguish soft tissues from synovial fluid due to their similar mass density, limiting the 3D assessment of soft tissues volume and thickness. This study aimed to evaluate a lead chromate contrast agent for μCΤ arthrography of rat knee joints ex vivo.DesignIntact tibiofemoral rat joints were injected with the contrast agent at different concentrations and imaged using a μCT at 2.7 μm isotropic voxel size. Cartilage thickness was measured using an automated procedure, validated against histological measurements, and analyzed as a function of μCT image resolution. Changes in hard and soft tissues were also analyzed in tibiofemoral joints 4 weeks after surgical destabilization of the medial meniscus (DMM).ResultsThe contrast agent diffused well throughout the whole knee cavity without penetrating the tissues, therefore providing high contrast at the boundaries between soft tissues and synovial fluid space. Thickness analysis of cartilage demonstrated a high similarity between histology and μ-arthrography approaches (R2 = 0.90). Four weeks after surgical DMM, the development of osteophytes (Oph) and cartilage ulcerations was recognizable with μCT, as well as a slight increase in trabecular bone porosity, and decrease in trabecular thickness.ConclusionsA lead chromate-based contrast agent allowed discriminating the synovial fluid from soft tissues of intact knee joints, and thus made possible both qualitative and quantitative assessment of hard and soft tissues in both intact and DMM tibiofemoral joints using high resolution μCT
Synthesis and Functionalization of Cyclic Sulfonimidamides: A Novel Chiral Heterocyclic Carboxylic Acid Bioisostere
SN 2018bsz: A Type I superluminous supernova with aspherical circumstellar material
We present a spectroscopic analysis of the most nearby Type I superluminous supernova (SLSN-I), SN 2018bsz. The photometric evolution of SN 2018bsz has several surprising features, including an unusual pre-peak plateau and evidence for rapid formation of dust greater than or similar to 200 d post-peak. We show here that the spectroscopic and polarimetric properties of SN 2018bsz are also unique. While its spectroscopic evolution closely resembles SLSNe-I, with early O II absorption and C II P Cygni profiles followed by Ca, Mg, Fe, and other O features, a multi-component H alpha profile appearing at similar to 30 d post-maximum is the most atypical. The H alpha is at first characterised by two emission components, one at similar to+3000 km s(-1) and a second at similar to - 7500 km s(-1), with a third, near-zero-velocity component appearing after a delay. The blue and central components can be described by Gaussian profiles of intermediate width (FWHM similar to 2000-6000 km s(-1)), but the red component is significantly broader (FWHM greater than or similar to 10000 km s(-1)) and Lorentzian. The blue H alpha component evolves towards a lower-velocity offset before abruptly fading at similar to + 100 d post-maximum brightness, concurrently with a light curve break. Multi-component profiles are observed in other hydrogen lines, including Pa beta, and in lines of Ca II and He I. Spectropolarimetry obtained before (10.2 d) and after (38.4 d) the appearance of the H lines shows a large shift on the Stokes Q - U plane consistent with SN 2018bsz undergoing radical changes in its projected geometry. Assuming the supernova is almost unpolarised at 10.2 d, the continuum polarisation at 38.4 d reaches P similar to 1.8%, implying an aspherical configuration. We propose that the observed evolution of SN 2018bsz can be explained by highly aspherical, possibly disk-like, circumstellar material (CSM) with several emitting regions. After the supernova explosion, the CSM is quickly overtaken by the ejecta, but as the photosphere starts to recede, the different CSM regions re-emerge, producing the peculiar line profiles. Based on the first appearance of H alpha, we can constrain the distance of the CSM to be less than similar to 6.5 x 10(15) cm (430 AU), or even lower (less than or similar to 87 AU) if the pre-peak plateau is related to an eruption that created the CSM. The presence of CSM has been inferred previously for other SLSNe-I, both directly and indirectly. However, it is not clear whether the rare properties of SN 2018bsz can be generalised for SLSNe-I, for example in the context of pulsational pair instability, or whether they are the result of an uncommon evolutionary path, possibly involving a binary companion
Asymmetric Synthesis of a Glucagon Receptor Antagonist via Friedel–Crafts Alkylation of Indole with Chiral α‑Phenyl Benzyl Cation
Development of a practical asymmetric synthesis of a
glucagon receptor
antagonist drug candidate for the treatment of type 2 diabetes is
described. The antagonist consists of a 1,1,2,2-tetrasubstituted ethane
core substituted with a propyl and three aryl groups including a fluoro-indole.
The key steps to construct the ethane core and the two stereogenic
centers involved a ketone arylation, an asymmetric hydrogenation via
dynamic kinetic resolution, and an <i>anti</i>-selective
Friedel–Crafts alkylation of a fluoro-indole with a chiral
α-phenyl benzyl cation. We also developed two new efficient
syntheses of the fluoro-indole, including an unusual Larock-type indole
synthesis and a Sugasawa-heteroannulation route. The described convergent
synthesis was used to prepare drug substance in 52% overall yield
and 99% ee on multikilogram scales
Asymmetric Synthesis of a Glucagon Receptor Antagonist via Friedel–Crafts Alkylation of Indole with Chiral α‑Phenyl Benzyl Cation
Development of a practical asymmetric synthesis of a
glucagon receptor
antagonist drug candidate for the treatment of type 2 diabetes is
described. The antagonist consists of a 1,1,2,2-tetrasubstituted ethane
core substituted with a propyl and three aryl groups including a fluoro-indole.
The key steps to construct the ethane core and the two stereogenic
centers involved a ketone arylation, an asymmetric hydrogenation via
dynamic kinetic resolution, and an <i>anti</i>-selective
Friedel–Crafts alkylation of a fluoro-indole with a chiral
α-phenyl benzyl cation. We also developed two new efficient
syntheses of the fluoro-indole, including an unusual Larock-type indole
synthesis and a Sugasawa-heteroannulation route. The described convergent
synthesis was used to prepare drug substance in 52% overall yield
and 99% ee on multikilogram scales
Highly Enantioselective Diels−Alder Reactions of Danishefsky Type Dienes with Electron-Deficient Alkenes Catalyzed by Yb(III)-BINAMIDE Complexes
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