نتایج جستجو برای: dissolution rate
تعداد نتایج: 977513 فیلتر نتایج به سال:
− Fenofibrate has been used for many years to lower cholesterol levels and its pharmacokinetic profile is well understood. However, due to its low solubility in water, it has low bioavailability after oral administration. In order to improve the dissolution rate, fenofibrate was formulated into a self-microemulsifying drug delivery systems (SMEDDS). We used pseudo-ternary phase diagrams to eval...
the in vitro dissolution of plasma-sprayed hydroxyapatite (pha) coatings with different characteristics, produced by various spraying conditions, in a tris-buffered solution at ph 7.4 was experimentally studied through the measurement of calcium ions release with inductively coupled plasma atomic emission spectroscopy (icp-aes), and then modeled. three coating characteristics, the crystallinity...
In vitro dissolution behaviors of CaTiO3 thin films deposited with ion beam assisted deposition (IBAD) and sputter-deposition techniques were investigated using Rutherford backscattering spectrometry (RBS) and Auger electron spectroscopy (AES). In vitro test was carried out by immersion in a simulated body fluid at 37 C for 5, 24, and 888 h. The dissolution of titanium ions from CaTiO3 film was...
Biorelevant in vitro dissolution is a useful technique for qualitative forecasting of the in vivo behavior of a formulation. A biorelevant dissolution medium for simvastatin was developed with a lower concentration of surfactant (0.1% sodium lauryl sulfate, SLS) in the medium as compared with the 0.5% SLS concentration stated in the USP monograph. The slower dissolution rate of simvastatin tabl...
Background and purpose: The increasing effect of liquisolid systems on dissolution behavior of poor soluble drugs has been proved. In this research, the effect of glycerin, as a nonvolatile solvent, on release profile of indomethacin was evaluated. Materials and methods: The Avicel as carrier and silica as coating powder material in 20: 1 ratio were used. Indomethacin was dispersed in glyc...
The present study deals with characterization of dispersions of a poorly water-soluble drug, celecoxib (CLX) in polyvinyl caprolactame-polyvinyl acetate-polyethylene glycol graft copolymer (Soluplus(®) (SOL)) prepared by different techniques. Dispersions of CLX in SOL at different ratios (2:1, 1:1, 1:2, 1:4 and 1:6) were prepared by spray drying, conventional solvent evaporation and melting met...
At oxic/anoxic transition zones, manganese release from (hydr)oxide minerals into aqueous solution is a dynamic balance between mineral dissolution and Mn2+(aq) oxidation and precipitation, which are processes respectively promoted by organic reductants and molecular oxygen. We employ a flow-through atomic force microscope reactor (AFM-R) to investigate the reductive dissolution of the [010] su...
the effects of crystallization of indomethacin as a poorly water-soluble drug in aqueous surfactant solutions (using the basket method), on the drug dissolution behavior was investigated.a significant enhancement of drug dissolution was observed for for the dissolution rates of crystals treated with hydrophilic surfactants, tween 80 and sodium lauryl sulfate (sls). however, asing arlacel 60 as ...
The present research was aimed to develop the meclizine hydrochloride-polyethylene glycol 20000 solid dispersions to enhance the solubility and dissolution rate. They were prepared using solvent evaporation method and evaluated for solubility studies, drug-carrier compatibility studies and in vitro dissolution studies. From the solubility studies, formulation F4 was selected to prepare the fast...
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