… over time and the remaining drug in the barrier at the end of … dissolution/absorption profiles
in DissolvIt. This study indicates that DissolvIt simulates dissolution and absorption of drugs in …

… dissolution systems and absorption models, which have been developed to evaluate dry
powder … , various in vitro dissolution testing methods developed for dry powder particles, and …

… process of absorption of drug from oral route dissolution is … drug powder is therefore
deagglomerated in the dry state. This may be used to increase the dissolution rate of drug powders …

… , the choice of a suitable dissolution medium Tool for Oral Drug Absorption: … dissolution of
two drug powders was highly dependent process in vivo and to predict oral drug absorption (9,…

… drug dissolution characteristics of powders. Figure 3 represents a typical drug dissolution
profile for the amount of drug dissolved … dissolution limitations to the oral absorption of drugs in …

… On the other hand, prolonged dissolution and slow absorption can increase drug residence
time in the airways and favor local therapeutic effect, depending on the deposition site and …

… of EZ from the EZ/LAC and EZ/MAN microparticles was markedly faster than that from EZ
powder, and the dissolution was faster at lower ratios of EZ. Considering the crystalline state of …

… absorption process is limited by drug dissolution rate in gastrointestinal media. Therefore,
enhancement of the dissolution rate of these drugs … drug powder transfer to an ultrafine powder …

… dissolution rate and subsequently the oral absorption and bioavailability of a model poorly
water-soluble drug… The powder collected was again stored in a desiccator until it was ready to …

… dissolution conditions and changing drug particle surface area to give a more realistic simulation
of drug dissolution in … the model to handle polydisperse drug powders, particle size and …