... SMEDDS are a promising approach for the formulation of drugs with poor aqueous solubility. The oral delivery of hydrophobic drugs can be made possible by SMEDDS, which have been shown to substantially improve oral ...
... the drug and is closed by an erodible tablet ...that drug release from the pulsatile capsule exhibited an initial lag period, followed by a stage of rapid drug ...rapid drug release from the ...
... this drug since the incidence of G6PD genetic anomaly is particularly high in areas where malaria is endemic, 35 a situation that calls for new methods addressed to the targeted delivery of PQ active ...
... The drug release from the bees wax microspheres was found sufficient for oral delivery and the drug release profile was significantly affected by the properties of wax used in the prepar[r] ...
... A blend of PDEA based hydrogel with polyurethane was prepared having good film forming properties and adequate for drugdelivery applications. The blending of PDEA with PU modifies the interactions as ...
... drugs. Drug release rate of the high amylose starch excipients crosslinked using epichlorohydrin has been reported to increase with increasing cross-linking degree of the polymer (Lenaerts et al, ...
... of self-deception. We have shown in this study that self-deception in addicts tends to become chronic or dissolve depending on the presence of addiction- related and craving core ...that ...
... Results. Many of the drugs employed for the treatment of neurodegenerative diseases are not capable of going through the blood-brain-barrier (BBB) and reach the brain with enough concentration, being unable to apply ...
... of drug released from Ibuprofen osmotic drugdelivery system coated with cellulose acetate membrane was ...percentage drug release of osmotic pump controlled Ibuprofen tablet using 10 % and 20 ...