On the influence of solid-liquid mass transfer in the modelling of drug release from stents

In this paper we present a model of drug release from a drug eluting-stent and the subsequent drug transport in the arterial wall. In order to study the complete process, a two-phase mathematical model describing the transport of a drug between two coupled media of different properties and dimensions is presented. A system of partial differential equations describes both the solid-liquid transfer (dissolution) and diffusion processes in the polymeric substrate as well as diffusion, convection and reaction in the tissue layer.

Modelling the glycocalyx-endothelium-erythrocyte interaction in the microcirculation: a computational study

A novel, coarse-grained, single-framework 'Eulerian' model for blood flow in the microvascular circulation is presented and used to estimate the variations in flow properties that accrue from all of the following: (i) wall position variation, associated with the endothelial cells' (ECs) shape, (ii) glycocalyx layer (GL) effects and (iii) the particulate nature of blood. We stress that our new model is fully coupled and uses only a single Eulerian computational framework to recover complex effects, dispensing altogether with the need for, e.g. re-meshing and advected sets of Lagrangian points.

A general model of coupled drug release and tissue absorption for drug delivery devices

In this paper we present a general model of drug release from a drug delivery device and the subsequent transport in biological tissue. The model incorporates drug diffusion, dissolution and solubility in the polymer coating, coupled with diffusion, convection and reaction in the biological tissue. Each layer contains bound and free drug phases so that the resulting model is a coupled two-phase two-layer system of partial differential equations. One of the novelties is the generality of the model in each layer.

A 1D mechanistic model can predict duration of in-vivo drug release from drug-eluting stents

We present a general model of drug release from a drug delivery device and the subsequent transport in biological tissue. The model incorporates drug diffusion, dissolution and solubility in the polymer coating, coupled with diffusion, convection and reaction in the biological tissue. Each layer contains bound and free drug phases so that the resulting model is a coupled two-phase two-layer system of partial differential equations. One of the novelties is the generality of the model in each layer.

Chronology protection in the Kerr metric

We show that causality violation in a Kerr naked singularity spacetime is constrained by the existence of (radial) potential barriers. We extend to the class of vortical non-equatorial null geodesics confined to $$\theta $$? $$=$$= constant hyperboloids (boreal orbits) previous results concerning timelike ones (Calvani et al. in Gen Rel Gravit 9:155, 1978), showing that within this class of orbits, the causality principle is rigorously satisfied.