Controlling release from encapsulated drug-loaded devices: insights from modeling the dissolution front propagation
Dissolution of drug from its solid form to a dissolved form is an important consideration in the design and
optimization of drug delivery devices, particularly owing to the abundance of emerging compounds that are
extremely poorly soluble. When the solid dosage form is encapsulated, for example by the porous walls of an
implant, the impact of the encapsulant drug transport properties is a further confounding issue. In such a case,
dissolution and diffusion work in tandem to control the release of drug.