Syncytia are multinucleated cells that can occur due to virus infection of cells. Mathematical models in the form of ordinary differential equations can be used to simulate the growth of syncytia. Several novel ODE models can explain syncytia growth. Before employing these models on actual data, it is essential to analyze their structural (theoretical) and practical identifiability using computer software. Structural identifiability is an inherent property of each model and its parameters, referring to our ability to determine parameter values for the model given particular experimental measurements. Practical Identifiability analysis of a model is concerned with determining our ability to accurately determine parameter values given experimental error. Combining these two techniques enables us to determine whether or not the parameters of our syncytia models can be accurately determined. Obtaining accurate parameter values allows us to make conclusions about our data that can provide insight into the nature of the spread of syncytia. From this, we can plan experiments to parameterize the syncytia growth in the contexts of our models.

Mpox virus is a type of virus similar to smallpox that can cause diseases in humans. Several experiments have been done to collect data on how mpox evolves within an infected host. This data can be analyzed within the context of mathematical models to determine important characteristics of mpox. From this analysis, we can estimate the growth rate, reproduction number, and infecting time of mpox.  We can also construct confidence intervals to estimate the error in our predictions using bootstrapping.  Bootstrapping allows us to analyze parameter correlations within mpox data to understand how parameter values within the model affect each other in our model. From these values and confidence intervals, we can learn about how mpox evolves within the body over time. This information, in turn, may allow us to make predictions on how mpox evolves within people during infection that could inform future treatment regimens.

Iron zinc oxides are multifunctional materials with applications in luminescent devices, catalysis, spintronics, and gas sensors. Specifically, iron-doped zinc oxide (FeZnO) combines magnetic and chemical stability properties, making it suitable for technological and environmental applications. This study explores how synthesis parameters, including pH and dopant concentration, influence the morphology and properties of FeZnO nanoparticles. Hydrothermal synthesis was employed to prepare FeZnO with iron doping concentrations ranging from 1–10% and ZnO. Morphological and compositional analyses were performed using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). We also observed doped FeZnO antibacterial action for some of the synthesized samples in e-coli cultures. Future work will focus on improving dopant distribution, exploring antibacterial activity, and leveraging computational tools to refine material design for specific applications.

Oncolytic Herpes Simplex Viruses (oHSVs) target a wide range of different cells and specific mutations, allowing them to proliferate in tumor cells. Recent work has modified the virus to preferentially enter cells bearing epidermal growth factor receptors (EGFRs). This study focuses on characterizing the efficacy of different strains of EGFR-targeting oHSV by fitting a mathematical model that includes an interferon response to experimental data from U251 tumor-bearing mice. Using a combination of parameter fitting, optimization techniques, and ordinary differential equations (ODEs), we modeled tumor growth, viral dynamics, and immune response. Our findings suggest that an interferon-inclusive model best explains the growth and oHSV treatment of EGFR-bearing tumors. These results highlight the importance of immune interactions in oncolytic viral therapy and contribute to optimizing oHSV-based treatments for better clinical outcomes.

Among the most life-threatening diseases, cancer poses a major issue and affects over fifty million people worldwide. To overcome the challenges associated with conventional chemotherapy, affecting both cancerous and normal cells, here we develop folic acid-functionalized Graphene Quantum Dots (GQDs) targeted to folate receptors overexpressed in a variety of cancer cell lines. GQDs due to their high biocompatibility and intrinsic fluorescence-based imaging capabilities have recently emerged as promising theragnostic agents. In this project, we synthesized GQDs utilizing the bottom up synthesis method and functionalized them with folic acid. The efficacy of the Folic acid functionalized GQDs (FAGQDs) is evaluated through their internalization study in cancerous (HeLa) and normal (HEK-293) cells by utilizing the intrinsic fluorescence of FAGQDs.

The use of fluorescent compounds as biological markers or probes is widely used in assays for probing various properties, including but not limited to pH, temperature, or the presence of various proteins. This has allowed fluorescence to enter the fields of microscopy, diagnostics, and spectroscopy. Among the many dyes used for such applications are those that exhibit phosphorescence. Unlike fluorescence, which has a lifetime of several nanoseconds, phosphorescence lifetimes can be several seconds, allowing for the use of techniques such as gated detection, which can eliminate distracting background noise or Raman scattering. Since phosphorescence uses the triplet state rather than the singlet state, it requires less energy, which correlates with longer wavelengths. The phosphorescence emission of some dyes can extend from 425nm (blue) to 675nm (red), which encompasses almost the entire visible spectrum. This is especially useful when considering that longer wavelengths may be used when utilizing direct triplet state excitation, which allows for excitation wavelengths well into the visible range. The ability to utilize longer excitation wavelengths has numerous possibilities, among which include being safe to use with live cells, which opens the door for using phosphorescence as a technique for biological imaging. Not only does phosphorescence allow imaging to occur at longer wavelengths, which mitigates damage to cells and minimizes exposure to harmful ultraviolet radiation, but it also allows for much more affordable equipment and procedures, possibly making diagnostic care more accessible.

Multipartite viruses are a unique class of viruses that divide their genome into multiple segments, each packaged into a separate viral particle. Unlike traditional viruses, which encapsulate their entire genome within a single particle, multipartite viruses require all genome segments to infect the same host cell for successful replication. This study investigates the infection dynamics of multipartite viruses through mathematical modeling, with a focus on bipartite and tripartite viruses. By comparing their behavior to single-particle viruses, we analyze the factors influencing viral persistence and spread. Our results indicate that the higher number of particles in a virus, the harder it is to maintain an infection. While multipartite infections exhibit shorter durations of infections compared to single-particle infections, their ability to persist suggests a potential benefit. These findings can help develop an understanding into the adaptive mechanisms of multipartite viruses and contribute to a broader understanding of viral evolution and host-virus interactions.

Surface plasmon–coupled emission (SPCE) is a powerful phenomenon that utilizes the near-field interaction between excited fluorophores and thin metallic films, together with a glass substrate, to significantly improve fluorescence detection sensitivity. By coupling the fluorophore’s oscillating dipole to surface plasmons, SPCE channels a substantial fraction of the emitted photons into a defined angle, generating a highly directional and polarized emission that can achieve up to 50% light collection efficiency. This intrinsically wavelength-resolved emission not only simplifies optical system design but also elevates the signal-to-noise ratio by reducing background interference. Compared to conventional isotropic free-space fluorescence, SPCE’s strong directional control and enhanced collection enable the detection of analytes at extremely low limits. Hence, this paper elucidates how SPCE’s unique advantages can be leveraged to achieve highly sensitive detection of critical biomarkers, paving the way for more rapid and efficient diagnostic applications.

Micro- and nanoscale metal oxides are used in a variety of applications. ZnO and Ga2O3 semiconductors are two metal oxides that have a wide bandgap and find themselves used in today’s electronics, gas sensors, and photodetectors. These two materials are also used in a wide range of temperatures, which means that the chemical bond lengths, vibrational states, defect states, and band-gaps all should be variable. In our experiments, we investigate the T-dependencies of positions, intensities, and widths of Raman peaks/bands for micro- and nanoscale ZnO and Ga2O3. In our studies, in addition to the temperature-dependent Raman spectroscopy we employ scanning electron microscopy (morphology of particles), energy dispersive X-ray spectroscopy (stochiometry) and temperature-dependent photoluminescence spectroscopy (electronic structure).

Human Immunodeficiency Virus (HIV) can exist as syncytia-forming or non-syncytia-forming strains, each utilizing different mechanisms of infection. Understanding the competition between these strains is crucial, as syncytia formation has been linked to increased disease progression and immune system decline. This study develops a mathematical model to analyze their competition, incorporating parameters such as fusion rate, syncytia lifespan, and viral production. Stability analysis and simulations will determine conditions under which one strain dominates or both coexist. By varying key parameters, we aim to understand how syncytia formation influences viral dynamics and infection persistence, providing insights into HIV pathogenesis and potential treatment strategies.