ramipril has been researched along with carbitol* in 1 studies
1 other study(ies) available for ramipril and carbitol
Article | Year |
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Development and bioavailability assessment of ramipril nanoemulsion formulation.
The objective of our investigation was to design a thermodynamically stable and dilutable nanoemulsion formulation of Ramipril, with minimum surfactant concentration that could improve its solubility, stability and oral bioavailability. Formulations were taken from the o/w nanoemulsion region of phase diagrams, which were subjected to thermodynamic stability and dispersibility tests. The composition of optimized formulation was Sefsol 218 (20% w/w), Tween 80 (18% w/w), Carbitol (18% w/w) and standard buffer solution pH 5 (44% w/w) as oil, surfactant, cosurfactant and aqueous phase, respectively, containing 5 mg of ramipril showing drug release (95%), droplet size (80.9 nm), polydispersity (0.271), viscosity (10.68 cP), and infinite dilution capability. In vitro drug release of the nanoemulsion formulations was highly significant (p<0.01) as compared to marketed capsule formulation and drug suspension. The relative bioavailability of ramipril nanoemulsion to that of conventional capsule form was found to be 229.62% whereas to that of drug suspension was 539.49%. The present study revealed that ramipril nanoemulsion could be used as a liquid formulation for pediatric and geriatric patients and can be formulated as self-nanoemulsifying drug delivery system (SNEDDS) as a unit dosage form. Topics: Administration, Oral; Angiotensin-Converting Enzyme Inhibitors; Animals; Biological Availability; Buffers; Capsules; Chemistry, Pharmaceutical; Drug Compounding; Drug Stability; Emulsions; Ethylene Glycols; Hydrogen-Ion Concentration; Male; Models, Biological; Nanoparticles; Oils; Pharmaceutical Solutions; Phase Transition; Polysorbates; Ramipril; Rats; Rats, Wistar; Solubility; Surface-Active Agents; Technology, Pharmaceutical; Thermodynamics; Viscosity | 2007 |