Back Cover: Focus ion beam tomography reveals subsurface multiwall carbon nanotubes in electrospun fibers that have preferentially segregated to the PMMA phase in a PDMS/PMMA blend. The carbon nanotubes could not be observed in single tomograms due to their orientation. The observed contrast is attributed to electron‐induced field effects. This is reported by Eva M. Campo, Douglas Yates, Benjamin Berson, Wudmir Rojas, Allen D. Winter, Mohan Ananth, Jorge J. Santiago‐Aviles and Eugene M. Terentjev, in article number https://doi.org/10.1002/mame.201600479.
Multimodal focused ion beam (FIB) imaging on a polydimethylsiloxane/poly(methyl methacrylate) (PMMA)/multiwall carbon nanotube (MWCNT) electrospun composite has been applied to discriminate the phase‐separated polymer blend and identify MWCNT fillers. Upon tomographic reconstruction, this discrimination has been possible through both atomic number and voltage contrast, the latter being enabled by preferential MWCNT segregation to PMMA. This study suggests that electrospinning could be affecting not only MWCNT alignment but also phase separation dynamics of immiscible polymers, yielding a porous structure throughout the fibers. This work opens the door to correlative materials science in polymer nanocomposites through FIB tomography, where voltage contrast is a main actor.
Mixed-type autoimmune hemolytic anemia (AIHA) is a term used to describe hemolysis occurring in the context of both warm and cold reactive autoantibodies to red blood cells. Immune thrombocytopenia (ITP) is an acquired form of thrombocytopenia potentially complicated by hemorrhage due to autoantibodies reactive with platelets and megakaryocytes. Diagnosis of ITP requires exclusion of other known causes of thrombocytopenia. AIHA and ITP may be primary disorders or associated with lymphoproliferative, autoimmune, or viral infections. Here, we report a rare case of simultaneous mixed-type autoimmune hemolytic anemia with immune thrombocytopenia following severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection treated with Paxlovid followed by Rhinovirus infection.
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