Repaglinide (REP) loaded solid-lipid nanoparticles (SLNs) for intranasal administration is
the subject of the current work aiming enhancement of diabetes pharmacotherapy. SLNs …

Repaglinide (RPG) is poorly water soluble drug BCS (Low solubility, High permeability). The
objective of this study was to enhance the dissolution of RPG for oral drug delivery. RPG …

Background Association of long hydrocarbon chain with alginate molecule imparts surface
active properties and increases chain flexibility. Purpose This work studied the efficacy of …

The recent work primarily set out to evaluate and synthesize the Repaglinide (RG) solid
dispersion. The medicine rifampicin is classified as a class II biopharmaceutical due to its …

The recent study's objective was to prepare and evaluate the Repaglinide (RG) solid
dispersion. RG is poorly water soluble, BCS class II drug. Repaglinide solid dispersion (RG …

The purpose of this research work was to improve the aqueous solubility and dissolution
rate of carbamzepine by solid dispersion (SD) technique. Polyethylene Glycol 6000 …

The objective of this research was to develop a liquisolid (LS) formulation of dl-α tocopherol
acetate with improved dissolution properties and evaluate its strength to excipient …

The main aim and objective of present investigation was to formulate and evaluate pulsatile
drug delivery system for Antiinflammatory drugs like piroxicam. Chrono modulated drug …

Oral drug delivery is the most widely used route of administration for decades among all the
routes that have been employed for the systemic delivery of drug via various pharmaceutical …