نتایج جستجو برای: release study

تعداد نتایج: 4123954  

The aim of this study was to develop a derivative of chitosan as pharmaceutical excipient used in sustained-release matrix tablets of poorly soluble drugs. A water-soluble quaternary ammonium carboxymethylchitosan was synthesized by a two-step reaction with carboxymethylchitosan (CMCTS), decylalkyl dimethyl ammonium and epichlorohydrin. The elemental analysis showed that the target product with...

HR Patel MM Patel

The aim of the present study was to prepare and evaluate an osmotically controlled mucoadhesive cup-core (OCMC) containing aceclofenac. A special technique was used while preparing an OCMC. Stability of OCMC was determined in natural human saliva, and it was found that both pH and device are stable in human saliva. OCMC was evaluated by weight uniformity, thickness, hardness, friability, swelli...

Journal: :iranian journal of pharmaceutical research 0
p khazaeli f hassanzadeh

microencapsulation has become a common technique in the production of controlled release dosage forms. many results have been reported, concerning the use of alginate beads as controlled release drug formulations. alginate has a unique gel-forming property in the presence of multivalent cations, in an aqueous medium. ibuprofen is an excellent analgesic and antipyretic, non-steroidal anti-inflam...

Journal: :research in pharmaceutical sciences 0

the aim of the current study was to design a porous osmotic pump–based drug delivery system for controlling the release of buspirone from the delivery system. the osmotic pump was successfully developed using symmetric membrane coating. the core of the tablets was prepared by direct compression technique and coated using dip-coating technique. drug release from the osmotic system was studied us...

Journal: :journal of reports in pharmaceutical sciences 0
ehsan ahmadi behzad shabazi komail sadr javadi ali fattahi

a great challenge in using natural polysaccharide as drug delivery system is their fast drug release. the purpose of the present study was to prepare and evaluate chitosan oligosaccharide (cho)-de-estrifiedtragacanth (det) core-shell nanoparticles for controled release of water soluble drugs. cho-det nanoparticles were prepared by microemulsion method and characterized by ft-ir spectroscopy. si...

Journal: :iranian journal of basic medical sciences 0
fatemeh sadeghi department of pharmaceutics, school of pharmacy and pharmaceutical research center, mashhad university of medical sciences, mashhad, iran fatemeh mosaffa school of pharmacy, mashhad university of medical sciences, mashhad, iran hadi afrasiabi garekani department of pharmaceutics, school of pharmacy and pharmaceutical research center, mashhad university of medical sciences, mashhad, iran

objective eudragits are widely used polymers in the production of oral sustained release dosage forms. the application of these polymers in the production of inert insoluble matrices has been investigated. however the effect of particle size, compaction force and presence of aerosil 200 as a glidant on the properties of eudragit rs and rl matrices prepared by direct compression of their physica...

B Mazumder B Nath BP Sahu LK Nath N Sharma P Kumar

The aim of this study was to formulate and evaluate microencapsulated controlled release preparations of a highly water/soluble drug, salbutamol sulphate by (water in oil) in oil emulsion technique using ethyl cellulose as the retardant material. Various processing and formulation parameters such as drug/polymer ratio, stirring speed, volume of processing medium were optimized to maximize the e...

 Events leading up to the release of toxic chemicals in the processing plants are one of the main hazards of chemical industries that can endanger employees and also people in neighborhood. In this study, DOW's Chemical Exposure Index (CEI) is used to determine hazard distances of possible toxic chemical releases in one of the South Pars gas refineries. To...

Objective(s): The purpose of this study was preparation and evaluation of PVA-Fe3O4 nanofibers as nanocarrier of doxorubicin (DOX) by measuring their drug release together with their in vitro cytotoxicity toward cancer cells at different pH values. Methods: Fe3O4 nanoparticles were synthesized by coprecipitation...

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