TRAVELLING CHEMOTACTIC AGGREGATES AT MESOSCOPIC SCALE AND BISTABILITY

A model consisting of a kinetic equation for \run-and-tumble" biased bacteria motion, coupled with two reaction-diusion equations for chemical signals, is studied. It displays time- asymptotic propagation at constant velocity, i.e., aggregated travelling (exponential) layers. To capture them for various parameters, a well-balanced setup is based on both \Case's elementary solutions" and L-spline reconstruction. Far from the diusive regime, waves travelling at dierent velocities (bistability) are proved to coexist.

Linked Gauss-Diffusion processes for modeling a finite-size neuronal network

A Leaky Integrate-and-Fire (LIF) model with stochastic current-based linkages is considered to describe the firing activity of neurons interacting in a (2. ×. 2)-size feed-forward network. In the subthreshold regime and under the assumption that no more than one spike is exchanged between coupled neurons, the stochastic evolution of the neuronal membrane voltage is subject to random jumps due to interactions in the network. Linked Gauss-Diffusion processes are proposed to describe this dynamics and to provide estimates of the firing probability density of each neuron.

Mathematical modelling of variable porosity coatings for controlled drug release.

In this paper we investigate the extent to which variable porosity drug-eluting coatings can provide better control over drug release than coatings where the porosity is constant throughout. In particular, we aim to establish the potential benefits of replacing a single-layer with a two-layer coating of identical total thickness and initial drug mass. In our study, what distinguishes the layers (other than their individual thickness and initial drug loading) is the underlying microstructure, and in particular the effective porosity and the tortuosity of the material.

Combining Mathematical Modelling with In- Vitro Experiments to Predict In-Vivo Drug-Eluting Stent Kinetics,

In this paper we describe a combined in-vitro experimental and mathematical modelling approach to predict in-vivo drug-eluting stent kinetics. We coated stents with a mixture of sirolimus and a novel acrylic-based polymer in two different ratios. Our results indicate differential release kinetics between low and high drug dose formulations. Furthermore, mathematical model simulations of target receptor saturation suggest potential differences in efficacy.

Mathematical Modelling of Variable Porosity Coatings for Dual Drug Delivery

In this paper we describe a theoretical mathematical model of dual drug delivery from a durable polymer coated medical device. We demonstrate how the release rate of each drug may in principle be controlled by altering the initial loading configuration of the two drugs. By varying the underlying microstructure of polymer coating, further control may be obtained, providing the opportunity to tailor the release profile of each drug for the given application.

Alzheimer's disease: a mathematical model for onset and progression

In this article we propose a mathematical model for the onset and progression of Alzheimer's disease based on transport and diffusion equations. We regard brain neurons as a continuous medium and structure them by their degree of malfunctioning. Two different mechanisms are assumed to be relevant for the temporal evolution of the disease: i) diffusion and agglomeration of soluble polymers of amyloid, produced by damaged neurons and ii) neuron-to-neuron prion-like transmission.

Microscopic and macroscopic models for the onset and progression of Alzheimer's disease

In the first part of this paper we review a mathematical model for the onset and progression of Alzheimer's disease (AD) that was developed in subsequent steps over several years. The model is meant to describe the evolution of AD in vivo. In Achdou et al (2013 J. Math. Biol. 67 1369-92) we treated the problem at a microscopic scale, where the typical length scale is a multiple of the size of the soma of a single neuron. Subsequently, in Bertsch et al (2017 Math. Med. Biol.

GPU based detection of topological changes in Voronoi diagrams

The Voronoi diagrams are an important tool having theoretical and practical applications in a large number of fields. We present a new procedure, implemented as a set of CUDA kernels, which detects, in a general and efficient way, topological changes in case of dynamic Voronoi diagrams whose generating points move in time. The solution that we provide has been originally developed to identify plastic events during simulations of soft-glassy materials based on a lattice Boltzmann model with frustrated-short range attractive and mid/long-range repulsive-interactions.