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Adrianzen Alvarez, D.

Publications and source records attributed to Adrianzen Alvarez, D..

2 recordsLinked to original sources

Metrics for studying the porous void space of packed particles

Characterizing porosity in packed particle assemblies is a complex task that requires advanced analytical tools. We present a visually rich and extensive library of global, pore-based, and other metrics for analyzing features of porosity in such assemblies. Our library includes over 25 descriptors of "3D pores" that are identified using our LOVAMAP software. By applying our metrics to a set of simulated packings that vary by particle size, shape, and stiffness, we reveal predictable relationships between particle and void space characteristics. We identify two fundamental parameters of a monodisperse particle system - particle diameter ({delta}) and void volume fraction ({phi}) - that govern several void space features, such as the total number of bottlenecks (i.e., doors between pores), the median value of the largest enclosed sphere across all pores in a packing, and the fraction of reaction-center "hotspots." Through regression analyses on transformations of{delta} and{phi} , we quantify multiple packing-descriptor relationships, demonstrating, for example, that packing properties scale linearly with the median values of length-based descriptors across assemblies. We further introduce approaches for computing the number of vertices, edges, and faces of 3D pores, allowing for approximation to simpler polyhedra. Additional metrics explore surface entrances into the particle scaffold, traversable paths through the void space, and size-based accessibility. Together, these descriptors, which have been bundled into LOVAMAP, offer new insights into particle-pore architecture and spatial organization.

bioengineering↗

Polymer-assisted intratumoral delivery of ethanol: Preclinical investigation of safety and efficacy in a murine breast cancer model

Focal tumor ablation with ethanol could provide benefits in low-resource settings because of its low overall cost, minimal imaging technology requirements, and acceptable clinical outcomes. Unfortunately, ethanol ablation is not commonly utilized because of a lack of predictability of the ablation zone, caused by inefficient retention of ethanol at the injection site. To create a predictable zone of ablation, we have developed a polymer-assisted ablation method using ethyl cellulose (EC) mixed with ethanol. EC is ethanol-soluble and water-insoluble, allowing for EC-ethanol to be injected as a liquid and precipitate into a solid, occluding the leakage of ethanol upon contact with tissue. The aims of this study were to compare the 1) safety, 2) release kinetics, 3) spatial distribution, 4) necrotic volume, and 5) overall survival of EC-ethanol to conventional ethanol ablation in a murine breast tumor model. Non-target tissue damage was monitored through localized adverse events recording, ethanol release kinetics with Raman spectroscopy, injectate distribution with in vivo imaging, target-tissue necrosis with NADH-diaphorase staining, and overall survival by proxy of tumor growth. EC-ethanol exhibited decreased localized adverse events, a slowing of the release rate of ethanol, more compact injection zones, 5-fold increase in target-tissue necrosis, and longer overall survival rates compared to the same volume of pure ethanol. A single 150 {micro}L dose of 6% EC-ethanol achieved a similar survival probability rates to six daily 50 {micro}L doses of pure ethanol used to simulate a slow-release of ethanol over 6 days. Taken together, these results demonstrate that EC-ethanol is safer and more effective than ethanol alone for ablating tumors. Graphical AbstractThe inclusion of ethylcellulose limits extra-tumoral leakage of ethanol and increases the target-tissue ablation. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=102 SRC="FIGDIR/small/123125v1_ufig1.gif" ALT="Figure 1"> View larger version (29K): org.highwire.dtl.DTLVardef@172afb5org.highwire.dtl.DTLVardef@6d96deorg.highwire.dtl.DTLVardef@cbdf9borg.highwire.dtl.DTLVardef@c56187_HPS_FORMAT_FIGEXP M_FIG C_FIG

cancer biology↗