Mucoadhesive polymeric (carbopol 934) suspension of ciprofloxacin was prepared by
ultrasonication and optimized with the aim of developing an oral controlled release gastro …

Glipizide (GLZ) is an oral hypoglycemic agent, which is a weakly aqueous soluble drug. The
solubility values of GLZ in various neat solvents are scarce in the literature. Hence, the …

Baicalin-polyvinylpyrrolidone (PVP) coprecipitate was prepared by the solvent method of
solid dispersion technology to improve the dissolution rate of baicalin. The coprecipitate was …

Abstract Poly (2-ethyl-2-oxazoline)(PEOX), a biocompatible polymer considered as
pseudopolypeptide, was introduced as a potential alternative to the commonly used …

Background: Eprosartan mesylate (EM) is a poorly aqueous soluble drug belonging to BCS-
class II suffers from low bioavailability (13%). The present study involves an effort for …

Methods: The ciprofloxacin and Carbopol were mixed in water in a drug: polymer ratio of 1: 5
(w/w) and homogenized to produce uniform composites. X-ray powder diffraction analysis of …

The most crucial variable that affects a drug's bioavailability is its aqueous solubility. One of
the most significant issues facing the pharmaceutical business is improving water solubility …

Praziquantel (PZQ) is an anthelmintic of choice in the treatment of schistosomiasis. Solvent
evaporation technique produced three different Solid Dispersions (SD)(drug: polymer, w/w) …

In the present study various crystalline forms of glipizide were prepared in order to enhance
dissolution rate of glipizide and to evaluate the stability of developed forms. Four different …

Disintegration and dissolution are the in vitro performance test procedures for a drug to be
developed and its formulation to be selected for in vivo studies, specifically for orally …