Binary polymeric amorphous carvedilol solid dispersions were prepared using solvent
method by varying solvent type, polymer type and carvedilol to polymer ratio in order to …

Aim: To investigate the potential of a thermosensitive intranasal formulation of raloxifene
hydrochloride (RH) for systemic delivery with the possibility of enhanced bioavailability and …

This investigation was undertaken to unveil the controlled drug delivery and preclinical anti-
hypertensive potential of a novel interpenetrating biopolymer-based network of karaya gum …

Objective: To design and develop liquid and solid self-nanoemulsifying drug delivery
systems (SNEDDS and S-SNEDDS) of felodipine (FLD) using Box–Behnken design (BBD) …

This study aimed to prepare colloidosome particles loaded with pyrazinamide (PZA). These
drug-loaded colloidosomes were prepared using an in situ gelation technique using a …

The study aimed to design and develop carvedilol loaded silk fibroin-casein nanoparticles
using 3 2 full factorial design. Silk fibroin and casein concentration were selected as the …

Lacidipine (LCDP) is a calcium-channel blocker with low aqueous solubility and
bioavailability. Nanoemulsion (NE) is one of the popular methods that has been used to …

This study demonstrates the use of factorial design for the preparation of microsponges of
carvedilol with nanometric pores using the response surface methodology and to establish …

The amorphous form of carvedilol phosphate (CVD) was obtained as a result of grinding.
The identity of the obtained amorphous form was confirmed by powder X-ray diffraction …

Background In the current work, co-rotating twin-screw processor (TSP) was utilized to
formulate solid crystal suspension (SCS) of carvedilol (CAR) for enhancing its solubility …