A Novel Rat Model to Simulate Positive Margins in the Wound Bed of a Resected Sarcoma.

Background: One reason for local recurrence is the presence of positive surgical margins after tumor resection. An animal model accurately representing the microtumor burden will improve our understanding of these surgical margins. Using a rat model, we report a new methodology for creating microscopic tumors.

Hybrid Core-Shell TiCN@SiO Nanoparticles in Percolation-Based Polyvinylidene Fluoride Dielectrics for Improved High-Voltage Capacitive Energy Storage.

Solid-state polymer dielectrics offer an exceptional dielectric breakdown, but require an enhanced energy density to be competitive with alternative electrolyte-based energy storage technologies. Therefore, this research introduces conductive titanium carbonitride (TiCN) nanoparticles in a polyvinylidene fluoride (PVDF) matrix to obtain flexible percolation-based nanodielectrics by ultrasonication-based suspension processing and hot pressing. Well-dispersed TiCN nanoparticles in PVDF were obtained for a wide range of filler volume fractions, and an exceptional peak in the dielectric constant equal to 1130 (0.

Opportunities in optical and electrical single-cell technologies to study microbial ecosystems.

New techniques are revolutionizing single-cell research, allowing us to study microbes at unprecedented scales and in unparalleled depth. This review highlights the state-of-the-art technologies in single-cell analysis in microbial ecology applications, with particular attention to both optical tools, i.e.

Full-electric microfluidic platform to capture, analyze and selectively release single cells.

Current single-cell technologies require large and expensive equipment, limiting their use to specialized labs. In this paper, we present for the first time a microfluidic device which demonstrates a combined method for full-electric cell capturing, analyzing, and selectively releasing with single-cell resolution. All functionalities are experimentally demonstrated on .

L-asparaginase anti-tumor activity in pancreatic cancer is dependent on its glutaminase activity and resistance is mediated by glutamine synthetase.

l-Asparaginase is a cornerstone of acute lymphoblastic leukemia (ALL) therapy since lymphoblasts lack asparagine synthetase (ASNS) and rely on extracellular asparagine availability for survival. Resistance mechanisms are associated with increased ASNS expression in ALL. However, the association between ASNS and l-Asparaginase efficacy in solid tumors remains unclear, thus limiting clinical development.