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Accurate evaluation of morphological changes in articular cartilage are necessary for early detection of osteoarthritis (OA). 3T magnetic resonance imaging (MRI) has highly sensitive contrast resolution and is widely used clinically to detect OA. However, synchrotron radiation phase-contrast imaging computed tomography (SR-PCI) can also provide contrast to tissue interfaces that do not have sufficient absorption differences, with the added benefit of very high spatial resolution. Here, MRI was compared with SR-PCI for quantitative evaluation of human articular cartilage. Medial tibial condyles were harvested from non-OA donors and from OA patients receiving knee replacement surgery. Both imaging methods revealed that average cartilage thickness and cartilage volume were significantly reduced in the OA group, compared to the non-OA group. When comparing modalities, the superior resolution of SR-PCI enabled more precise mapping of the cartilage surface relative to MRI. As a result, MRI showed significantly higher average cartilage thickness and cartilage volume, compared to SR-PCI. These data highlight the potential for high-resolution imaging of articular cartilage using SR-PCI as a solution for early OA diagnosis. Recognizing current limitations of using a synchrotron for clinical imaging, we discuss its nascent utility for preclinical models, particularly longitudinal studies of live animal models of OA. [ABSTRACT FROM AUTHOR]

Purpose: Multiple-image radiography (MIR) is an analyzer-based synchrotron X-ray imaging approach capable of dissociating absorption, refraction, and scattering components of X-ray interaction with the material. It generates additional image contrast mechanisms (besides absorption), especially in the case of soft tissues, while minimizing absorbed radiation dose. Our goal is to develop a contrast agent for MIR using ultrasound microbubbles by carrying out a systematic assessment of size, shell material, and concentration. Procedures: Microbubbles were synthesized with two different shell materials: phospholipid and polyvinyl-alcohol. Polydisperse perfluorobutane-filled lipid microbubbles were divided into five size groups using centrifugation. Two distributions of air-filled polymer microbubbles were generated: 2–3 µm and 3–4 µm. A subset of polymer microbubbles 3–4 µm had iron oxide nanoparticles incorporated into their shell or coated on their surface. Microbubbles were immobilized in agar with different concentrations: 5 × 107, 5 × 106, and 5 × 105 MBs/ml. MIR was conducted on the BioMedical Imaging and Therapy beamline at the Canadian Light Source. Three images were generated: Gaussian amplitude, refraction, and ultra-small-angle X-ray scattering (USAXS). The contrast signal was quantified by measuring mean pixel values and comparing them with agar. Results: No difference was detected in absorption or refraction images of all tested microbubbles. Using USAXS, a significant signal increase was observed with lipid microbubbles 6–10 µm at the highest concentration (p = 0.02), but no signal was observed at lower concentrations. Conclusions: These data indicate that lipid microbubbles 6–10 µm are candidates as contrast agents for MIR, specifically for USAXS. A minimum concentration of 5 × 107 microbubbles (lipid-shell 6–10 µm) per milliliter was needed to generate a detectable signal. [ABSTRACT FROM AUTHOR]

Aggregates of the diacid form of tetra(p-carboxyphenyl)porphyrin (TCPP) are found to be stabilized in aqueous solution at low pH in the presence of poly(vinyl alcohol). At pH values in the range from about 1 to 4, a split Sorer band is observed which is independent of counterion and tentatively assigned to a dimer species. As the pH is made lower than 1, the spectra evolve to reveal the presence of porphyrin aggregates. As in the case of the well-known aggregates of the related tetra(p-sulfonatophenyl)porphyrin (TSPP) diacid, the concentration of spectroscopically distinguishable aggregates increases with increasing ionic strength or decreasing pH. Unlike aggregates of TSPP, however, TCPP aggregates below pH 1 have visible absorption spectra which depend on the counterion, which is Cl[sup -] or NO[sub 3, sup -] in this study. In this work, we present visible absorption, light-scattering, and resonance Raman spectra of TCPP diacid in its monomer, dimer, and aggregated forms and attempt to understand the structural basis for counterion-dependent structure and excitonic coupling in the aggregates. Evidence is presented for intercalation of inorganic counterions between porphyrin molecules in the aggregate, an effect which to our knowledge has not been previously reported. [ABSTRACT FROM AUTHOR]

Using X-rays produced by a third generation synchrotron at the Pacific Northwest Consortium Collaborative Access Team (PNC-CAT), Advanced Photon Source (APS), Argonne National Laboratory, the distribution of Fe, Ni, Ga, and Ge in a sample of the Canyon Diablo iron meteorite has been mapped microscopically in situ with a 5 µm x 5 µm spatial resolution. The principal phases investigated were kamacite (α Fe/Ni alloy, <6 wt% Ni), cohenite [a carbide, (Fe, Ni, Co)3C], and schreibersite [a phosphide, (Fe,Ni)3P]. A non-microscopic X-ray absorption analysis at the P edge indicated the presence of both phosphide and phosphate in the sample. Extended X-ray absorption fine structure (EXAFS) analysis of Fe in kamacite reflects the known bcc structure of kamacite. EXAFS analysis of Ni, Ga, and Ge indicates that these elements substitute for Fe within the kamacite bcc structure. Absorption edge shifts for these same elements are generally small relative to the metals themselves, suggestive of a metallic environment. Initial findings also suggest that Ga preferentially partitions into schreibersite (phosphide) rather than cohenite (carbide), whereas Ge behaves differently and is found principally in the kamacite. These observations further the understanding of the Ge and Ga budget within the Canyon Diablo meteorite, and the work also illustrates the potential of the X-ray microprobe technique for the study of meteorites. Other potential uses of the X-ray microprobe are indicated. [ABSTRACT FROM AUTHOR]