… solubility of the compound is on dissolution rate. Low dissolution rate influenced by poor
aqueous solubility … This is particularly important in oral drug administration where dissolution …

… due to poor aqueous solubility include increased chances of food effect, more frequent
incomplete drug release from the … Enhancement of solubility, dissolution rate and bioavailability of …

… was to develop self emulsifying drug delivery systems (SEDDS) of glipizide and to convert
it into solid SEDDS (S-SEDDS) using Syloid ® 244 FP as adsorbent. Solubility study, ternary …

… Self-nanoemulsifying drug delivery system (SNEDDS) containing oil (Phosal 53 MCT), …
Lutrol-E400) was prepared to enhance solubility and dissolution of lutein. Ternary phase diagram …

… drugs to enhance their thermodynamic stability, solubilization capacity, in vitro dissolution,
drug delivery … , ocular and oral drug delivery of IND in order to enhance its permeation, …

… system (solid SNEDDS) has been explored to improve the solubility and dissolution profile
of … area for drug solubilization leading to an enhanced solubility and dissolution of glipizide. …

… It is insoluble in aqueous solution of pH 4 and below; it is very slightly soluble … enhance
solubility and dissolution of poorly soluble drug by formulating self microemulsifying drug delivery …

… The present study aimed to develop novel suspended self-nanoemulsifying drug delivery
system (Su-SNEDDS) to enhance the solubility and dissolution rate. The Su-SNEDDS was …

… aqueous solubility. Overall, these results indicated that developed SNEDDS could be
successfully used to enhance solubility and dissolution rate of poorly soluble drugs such as TDL. …

… Hence, pharmaceutical research that focus on improving the … by enhancing solubility and
dissolution rate of poorly water-… the drug release as a fine colloidal particle, resulting enhanced …