In this paper we develop two mathematical models to predict the release kinetics of a water soluble drug from a polymer/excipient matrix tablet. The first of our models consists of a random walk on a weighted graph, where the vertices of the graph represent particles of a drug, excipient and polymer, respectively. The graph itself is the contact graph of a multidisperse random sphere packing. The second model describes the dissolution and the subsequent diffusion of the active drug out of a porous matrix using a system of a partial differential equations. The predictions of both models show good qualitative agreement with experimental release curves. The models will provide tools for designing better controlled release devices
This paper presents a comparative study between the data collected in a drug dissolution experiment ...
In this paper a new model describing drug release from a polymer matrix tablet is presented. The uti...
In this paper a new model describing drug release from a polymer matrix tablet is presented. The uti...
A model for simulating the drug release from a swelling and dissolving polymer tablet is presented a...
A model for simulating the drug release from a swelling and dissolving polymer tablet is presented a...
2noThis paper deals with the physical and mathematical modelling description of drug release from ma...
A model for simulating the drug release from a swelling and dissolving polymer tablet is presented a...
This work deals with the modeling of drug release from solid pharmaceutical systems (matrices) for o...
This work deals with the modeling of drug release from solid pharmaceutical systems (matrices) for o...
This work deals with the modeling of drug release from solid pharmaceutical systems (matrices) for o...
This work deals with the modeling of drug release from solid pharmaceutical systems (matrices) for o...
In this work, mathematical models have been developed describing drug release from film-coated reser...
Hydrogels are materials largely used in the formulation of pharmaceuticals since, in principle, the...
The ability to develop predictive mathematical models of therapeutic release from pharmaceutical for...
Purpose: To study the effects of drug concentration and spatial distribution of the medicament, in p...
This paper presents a comparative study between the data collected in a drug dissolution experiment ...
In this paper a new model describing drug release from a polymer matrix tablet is presented. The uti...
In this paper a new model describing drug release from a polymer matrix tablet is presented. The uti...
A model for simulating the drug release from a swelling and dissolving polymer tablet is presented a...
A model for simulating the drug release from a swelling and dissolving polymer tablet is presented a...
2noThis paper deals with the physical and mathematical modelling description of drug release from ma...
A model for simulating the drug release from a swelling and dissolving polymer tablet is presented a...
This work deals with the modeling of drug release from solid pharmaceutical systems (matrices) for o...
This work deals with the modeling of drug release from solid pharmaceutical systems (matrices) for o...
This work deals with the modeling of drug release from solid pharmaceutical systems (matrices) for o...
This work deals with the modeling of drug release from solid pharmaceutical systems (matrices) for o...
In this work, mathematical models have been developed describing drug release from film-coated reser...
Hydrogels are materials largely used in the formulation of pharmaceuticals since, in principle, the...
The ability to develop predictive mathematical models of therapeutic release from pharmaceutical for...
Purpose: To study the effects of drug concentration and spatial distribution of the medicament, in p...
This paper presents a comparative study between the data collected in a drug dissolution experiment ...
In this paper a new model describing drug release from a polymer matrix tablet is presented. The uti...
In this paper a new model describing drug release from a polymer matrix tablet is presented. The uti...