Stainless-steel templates of various thicknesses (75, 200, 800, and 1600 µm) were used to apply propylene glycol/water gels containing methyl or propyl p -aminobenzoates to silicone rubber membranes, and drug delivery was studied with the use of the Bronaugh diffusion cell under conditions in which the drug was initially in thermodynamic equilibrium with respect to the application and membrane. Theoretical diffusion profiles were generated with the use of a model which assumes that diffusional gradients exist within the application. To use the model equation, previously derived for the initial condition in which the drug is in thermodynamic equilibrium with respect to the application and membrane, drug diffusivity in both the application an...
Topically applied anti-HIV microbicides are placed within a cultural, economic, and ethical context ...
In nanomedicine, an increasing interest has been allotted to local administration of drugs. For this...
In this paper we present a general model of drug release from a drug delivery device and the subsequ...
The mechanisms whereby drugs are delivered from thin applications into and through the skin are poor...
There are presently no standards for in vitro research dealing with the release and delivery of drug...
In order to understand the role of the formulation components in topical drug delivery it is necessa...
Regulatory approval of generic topical products is presently based upon extensive pharmacodynamic ef...
This chapter is aimed to illustrate and to discuss membrane applications in the delivery field focus...
Over recent decades, the use of in vitro diffusion cell studies to assess skin permeability has evol...
This thesis is concerned with the mathematical modelling of controlled drug release from a number of...
Synthetic membranes used in Franz diffusion cells for topical formulation quality assessment should ...
Purpose. The thermodynamic acitvity of drugs in topical vehicles is considered to significantly infl...
Purpose. In the present study we examined the relationship between solvent uptake into a model membr...
The aim of this study was to test the hypothesis that the most appropriate model for studying the di...
The aim of this study was to investigate the impact of formulation excipients and solubilizing addit...
Topically applied anti-HIV microbicides are placed within a cultural, economic, and ethical context ...
In nanomedicine, an increasing interest has been allotted to local administration of drugs. For this...
In this paper we present a general model of drug release from a drug delivery device and the subsequ...
The mechanisms whereby drugs are delivered from thin applications into and through the skin are poor...
There are presently no standards for in vitro research dealing with the release and delivery of drug...
In order to understand the role of the formulation components in topical drug delivery it is necessa...
Regulatory approval of generic topical products is presently based upon extensive pharmacodynamic ef...
This chapter is aimed to illustrate and to discuss membrane applications in the delivery field focus...
Over recent decades, the use of in vitro diffusion cell studies to assess skin permeability has evol...
This thesis is concerned with the mathematical modelling of controlled drug release from a number of...
Synthetic membranes used in Franz diffusion cells for topical formulation quality assessment should ...
Purpose. The thermodynamic acitvity of drugs in topical vehicles is considered to significantly infl...
Purpose. In the present study we examined the relationship between solvent uptake into a model membr...
The aim of this study was to test the hypothesis that the most appropriate model for studying the di...
The aim of this study was to investigate the impact of formulation excipients and solubilizing addit...
Topically applied anti-HIV microbicides are placed within a cultural, economic, and ethical context ...
In nanomedicine, an increasing interest has been allotted to local administration of drugs. For this...
In this paper we present a general model of drug release from a drug delivery device and the subsequ...