… Depending on the preparation procedure, drug-loaded … review, we summarize the classification
system of lipid formulations, the mechanism underlying improved oral drug absorption by …

… improving the oral bioavailability of nintedanib. Self-microemulsifying drug delivery systems
… stability are considered ideal alternative oral drug delivery carriers for drugs with poor …

… self-microemulsifying drug delivery system (SMEDDS) for the model active pharmaceutical
ingredient (API) dipyridamole using exclusively excipients suitable for oral administration and …

… In vitro dissolution assay indicated that dipyridamole in SNEDDS dissolved rapidly, while …
opment of self-microemulsifying drug delivery systems for oral bioavailability enhancement of …

… ‘self-microemulsifying drug–delivery systems’ (SMEDDS). Since, by definition, microemulsions
are formed spontaneously, the term ‘SMEDDS’ is meaningless [50]. On the other hand, …

… study is to develop sustained release of dipyridamole, a poorly soluble weakly basic compound.
The solubility of dipyridamole is the limit step of its bioavailability. To improve this, direct …

… Type III formulations are also known as self microemulsifying drug delivery systems. These
kinds of formulations can be further categorized into two types, named type III A and type III B. …

… Aim of the study was to prepare dipyridamole (DPM) cocrystals to alter its physicochemical
properties as it is poorly soluble in water, 6.8 pH buffer and belongs to BCS class II. …

… enhance the oral bioavailability of candesartan cilexetil by presenting the drug in a pre-solubilized
form ready for absorption… inhibition potential to enhance its oral delivery. Also, the …

… The present research was aimed at development and optimization of dipyridamole … Self-microemulsifying
drug delivery system for improved oral bioavailability of dipyridamole: …