… solubility in the ointment base faster than the diffusion speed of the dissolved drug particles
there. This assumption is important because diffused particle is immediately replaced by the …

… higher dissolution rate than … drug release than the physical mixture (p < 0.05) in time points
at 5 and 10 min. Besides, while all the samples showed fast dissolution behavior, the release …

… loading ASDs (≤10% DL) in this study, irrespective of polymer type, drug and polymer
release congruently with the dissolving tablet surface retaining its initial homogeneous …

… Therefore, the controlled-release effect and drug dissolution enhancement can be achieved
through polymer properties (such as degree of polymerization and degree of hydrolysis), …

… drug release properties and kinetics of the drug release model. Kinetic models help describe
the release … , optimizing the drug delivery device's design, evaluating the drug release rate, …

… drug release profiles can be divided into three stages according to the rate of drug release.
… the rate of PEG release also decreased, indicating that PEG dissolution was caused by fiber …

… Thus, during the above crosslink process, the dissolved drug in DMSO could be effectively
loaded inside the hydrogels' porous structures as an injectable peritumoral implant. The …

… drug release is a popular advanced drug controlled release … strong platform for developing
biphasic release dosage forms. In this … In vitro drug dissolution tests: a drug release profiles of …

… Moreover, poorly water soluble drugs like carvedilol and IBU loaded into PCL nanofibrous …
in dissolution 12 . To overcome the problem of dissolution and release of poor drug releasing …

… drug degradation and assure consistent deposition of drug-… The in-vitro drug release rate
was optimised by varying drug … to dissolution medium, thus, exhibited a fast drug release, ie …