نتایج جستجو برای: release studies

تعداد نتایج: 1608617  

M. Karthikeyan M.K. Deepa,

      The objective of the present study was to develop floating microspheres of cefpodoxime proxetil in order to achieve an extended retention in the upper GIT, which may result in enhanced absorption and thereby improved bioavailability. The microspheres were prepared by non-aqueous solvent evaporation method using polymers such as hydroxyl propyl methyl cellulose (HPMC K 15 M), ethyl cellulo...

Journal: :iranian journal of veterinary medicine 0
katayoun kiani phd student, department of pharmacology, faculty of veterinary medicine, university of tehran, tehran, iran. ali rassouli department of pharmacology, faculty of veterinary medicine, university of tehran, tehran, iran yalda hosseinzadeh ardakani department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran hamid akbari javar department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran sakineh khanamani falahatipour department of pharmacology, faculty of veterinary medicine, university of tehran, tehran, iran pegah khosraviyan department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran taghi zahraee salehi

background: sustained release delivery system can reduce the dosage frequency and maintain the therapeutic level of drugs for a longer time. biodegradable, biocompatible and thermosensitive chitosan-beta-glycerophosphate (c-gp) solutions can solidify at body temperature and maintain their physical integrity for a longer duration. objectives: to develop a novel delivery system based on the integ...

Journal: :iranian journal of pharmaceutical research 0
a attar nasseri r aboofazeli t needham t needham

ketorolac tromethamine (kt) containing microemulsion-based gels (mbgs) have been formulated, based on the previous phase diagram studies, using a pharmaceutically acceptable surfactant (soybean lecithin; epikuron 200) and oil (isopropyl myristate; ipm) and the effect of formulation variables on the release profile of the drug from mbgs through intact guinea pig skin and various artificial membr...

Journal: :nanomedicine research journal 0
mitra amoli diva department of chemistry, payam noor university (pnu), tehran, iran kamyar pourghazi department of novel medical technologies, darupakhsh pharmaceutical co., tehran, iran

objective(s): researchers have intended to reformulate drugs so that they may be more safely used in human body. polymer science and nanotechnology have great roles in this field. the aim of this paper is to introduce an efficient drug delivery vehicle which can perform both targeted and controlled antibiotic release using magnetic nanoparticles grafted ph-responsive polymer.  methods: fe3o4 na...

Journal: :iranian journal of pharmaceutical research 0
pankaj kumar soa university, bhubneshwar, orissa, india ashok laxmanrao ganure sahyadri college of pharmacy, sangola, solapur, india bharat bhusan subudhi school of pharmaceutical sciences, siksha o anusandhan university, bhubaneswar, india shubhanjali shukla department of pharmaceutics, indian institute of technology (banaras hindu university), varanasi, india

the present investigation deals with the development of controlled release tablets of salbutamol sulphate using graft copolymers (st-g-pmma and ast-g-pmma) of starch and acetylated starch. drug excipient compatibility was spectroscopically analyzed via ft-ir, which confirmed no interaction between drug and other excipients. formulations were evaluated for physical characteristics like hardness,...

بلورچیان, دکتر نوشین, داداش‌زاده, دکترسیمین, نصرالهی نصرآباد, دکتر اعظم,

Abstract Introduction: Preparation of tramadol HCl sustained release delivery system as an analgesic drug could improve its efficacy, reduce side effects and increase patient compliance. Objective: The aim of the present study was to prepare tramadol HCl loaded microspheres and coat them by solvent evaporation (ESE) method, in order to obtain an appropriate sustained release behavior and to p...

Journal: :research in pharmaceutical sciences 0
h v chavda m s patel c n patel

the objective of the present study was to design an oral controlled drug delivery system for sparingly soluble diclofenac sodium (dcl) using guar gum as triple-layer matrix tablets. matrix tablet granules containing 30% (d1), 40% (d2) or 50% (d3) of guar gum were prepared by the conventional wet granulation technique. matrix tablets of diclofenac sodium were prepared by compressing three layers...

Journal: :iranian journal of basic medical sciences 0
saieede soltani drug applied research center, tabriz university of medical sciences, tabriz, iran student research committee, tabriz university of medical sciences, tabriz, iran parvin zakeri-milani liver and gastrointestinal diseases research center, tabriz university of medical sciences, tabriz, iran department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, iran mohammad barzegar-jalali department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, iran mitra jelvehgari drug applied research center, tabriz university of medical sciences, tabriz, iran

objective(s): ketotifen fumarate (kf) is a selective and noncompetitive histamine antagonist (h1-receptor) that is used topically in the treatment of allergic conditions of rhinitis and conjunctivitis. the aim of this study was to formulate and improve an ophthalmic delivery system of kf.ocular nanoparticles were prepared with the objective of reducing the frequency of administration and obtain...

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