نتایج جستجو برای: drug release rate

تعداد نتایج: 1651239  

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

abstract ketotifen fumarate is a non-bronchodilator anti-asthmatic drug which inhibits the effects of certain endogenous substances known to be inflammatory mediators, and thereby exerts antiallergic activity. the present study describes the formulation of a sustained release nanoparticle (np) drug delivery system containing ketotifen, using poly (d,l lactide-co-glycolide acid) (plga). biodegra...

Ali Nokhodchi, Mitra Jelveghari Mohammad-Reza Siahi Siavoosh Dastmalchi

      Benzoyl peroxide (BPO) is a first-line topical treatment in acne vulgaris, and it is superior to antibiotics, because the bacteria do not develop resistance to it. Skin irritation is a common side effect, and it has been shown that controlled release of BPO from a delivery system to the skin could reduce the side effects while reducing percutaneous absorption. Therefore, the purpose of t...

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.<s...

Journal: :international journal of nanoscience and nanotechnology 2010
v. r. sinha d. ghai

the present work was aimed to design and develop self-nanoemulsifying drug delivery systems (snedds) with the objective to overcome the problems associated with the delivery of talinolol, a hydrophobic and poorly bioavailable drugs having ph dependant solubility. the solubility of talinolol in various oils, surfactants, cosurfactants and aqueous phases were determined to identify and select the...

Journal: :iranian journal of pharmaceutical research 0
z jaffariazar e damercheli

the aim of this study was preparation and evaluation of ciprofloxacin-containing minitablets for ocular use, in an attempt to obtain prolonged and controlled drug release to the anterior eye segment. following initial studies on ciprofloxacin powder, it was formulated into ocular minitablets. for this purpose, ciprofloxacin along with various amounts of different sustained release cellulose der...

E Damercheli SA Mortazavi Z Jaffariazar

The aim of this study was preparation and evaluation of ciprofloxacin-containing minitablets for ocular use, in an attempt to obtain prolonged and controlled drug release to the anterior eye segment. Following initial studies on ciprofloxacin powder, it was formulated into ocular minitablets. For this purpose, ciprofloxacin along with various amounts of different sustained release cellulose de...

E Damercheli SA Mortazavi Z Jaffariazar

The aim of this study was preparation and evaluation of ciprofloxacin-containing minitablets for ocular use, in an attempt to obtain prolonged and controlled drug release to the anterior eye segment. Following initial studies on ciprofloxacin powder, it was formulated into ocular minitablets. For this purpose, ciprofloxacin along with various amounts of different sustained release cellulose de...

Journal: :jundishapur journal of natural pharmaceutical products 0
abbas akhgari targeted drug delivery research center, school of pharmacy, mashhad university of medical sciences, mashhad, ir iran abdolmaohammad ghalambor dezfuli physics department, shahid chamran university, ahvaz, ir iran mohammadebrahim rezaei physics department, shahid chamran university, ahvaz, ir iran mohammad kiarsi nanotechnology research center, school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran mohammadreza abbaspour targeted drug delivery research center, school of pharmacy, mashhad university of medical sciences, mashhad, ir iran; targeted drug delivery research center, school of pharmacy, mashhad university of medical sciences, mashhad, ir iran. tel/fax: +98-5138823251

results the results showed that the fiber diameter and the amount of loratadine affected the drug release and the disappearance time of nanofibers. the smaller the fiber diameter and drug amount, the faster the solubility and the release time of nanofibers. conclusions it was concluded that electrospinning can be a suitable method for preparing fast-dissolving loratadine nanofibers. materials a...

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: :iranian journal of pharmaceutical research 0
reza masaeli dental biomaterials department, school of dentistry, tehran university of medical sciences, tehran, iran teherh sadat jafarzadeh kashi dental biomaterials department, school of dentistry, tehran university of medical sciences, tehran, iran rasoul dinarvand nanotechnology research centre, faculty of pharmacy, tehran university of medical sciences, tehran 1417614411, iran mohammadreza tahriri dental biomaterials department, school of dentistry, tehran university of medical sciences, tehran, iran vahid rakhshan department of anatomy, dental branch, islamic azad univesity mehdi esfandyari-manesh nanotechnology research center,tehran university of medical sciences, tehran, iran

microspheres formulated from poly (d,l-lactic-co-glycolide) (plga), a biodegradable polymer, have been extensively evaluated as a drug delivery system. in this study, the preparation, characterization and drug release properties of the plga microspheres were evaluated. simvastatin (sim)-loaded plga microspheres were prepared by oil-in-water emulsion/solvent evaporation method. the microspheres ...

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