نتایج جستجو برای: sustained drug release

تعداد نتایج: 840673  

Journal: :iranian journal of basic medical sciences 0
hadi afrasiabi garekani pharmaceutical research center, mashhad university of medical sciences, mashhad, iran department of pharmaceutics, school of pharmacy, mashhad university of medical sciences, mashhad, iran roshanak dolatabadi department of pharmaceutics, school of pharmacy, mashhad university of medical sciences, mashhad, iran abbas akhgari targeted drug delivery research center, mashhad university of medical sciences, mashhad, iran department of pharmaceutics, school of pharmacy, mashhad university of medical sciences, mashhad, iran mohammad reza abbaspour targeted drug delivery research center, mashhad university of medical sciences, mashhad, iran

objective(s): this study evaluates the effect of substitution of microcrystalline cellulose (mcc) with ethylcellulose (ec) on mechanical and release characteristics of theophylline pellets. materials and methods: the effect of addition of ec was investigated on characteristics of pellets with varying drug content prepared by extrusion-spheronization. also the effect of type of granulating liqui...

Journal: :iranian journal of pharmaceutical research 0
a kulkarni m bhatia

this study was performed to design bilayer regioselective floating tablets of atenolol and lovastatin to give immediate release of lovastatin and sustained release of atenolol. bilayer floating tablets comprised two layers, i.e immediate release and controlled release layers. the immediate release layer comprised sodium starch glycollate as a super disintegrant and the sustained release layer c...

Journal: :iranian journal of pharmaceutical sciences 0
n suresh assistant professor, department of pharmaceutics, sri k.v. college of pharmacy, chickballapur, karnataka, india bs ashok kumar department of pharmacognosy as kiran department of pharmaceutical chemistry n narayana swamy department of pharmaceutical chemistry d sheshadri shaker department of pharmacology, sri k.v. college of pharmacy, chickballapur, karnataka, india kv satish department of pharmaceutics

an oral suspension could a suitable dosage form for the geriatric patients. the calcium alginate coated ion exchange resinate of propranolol hydrochloride were prepared using amberlite ir-120 by solvent evaporation. microcapsules of propranolol hydrochloride resinate were prepared by solvent evaporation technique,the suspensions were prepared by using deionised water as the vehicle. methyl cell...

A Kulkarni M Bhatia

This study was performed to design bilayer regioselective floating tablets of atenolol and lovastatin to give immediate release of lovastatin and sustained release of atenolol. Bilayer floating tablets comprised two layers, i.e immediate release and controlled release layers. The immediate release layer comprised sodium starch glycollate as a super disintegrant and the sustained release layer c...

The present study deals with the fabrication of ibuprofen-mesoporous hydroxyapatite (IBU-MHA) particles via the incorporation of ibuprofen (IBU)—as a nonsteroidal anti-inflammatory drug—into mesoporous hydroxyapatite nanoparticles (MHANPs) using an impregnation process, as a novel drug delivery device. MHANPs were synthesized by a self-assembly process using cetyltrimethylammonium bromide (CTAB...

Journal: :research in pharmaceutical sciences 0
m jelvehgari m maghsoodi h nemati

the objective of the present investigation was to design a sustained release floating microcapsules of theophylline using two polymers of different permeability characteristics; eudragit rl 100 (eu rl) and cellulose acetate butyrate (cab) using the oil-in-oil emulsion solvent evaporation method. polymers were used separately and in combination to prepare different microcapsules. the effect of d...

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...

Journal: :iranian journal of pharmaceutical sciences 0
fatemah atyabi department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran afsaneh mohammadi department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran rassoul dinarvand department of pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran

the purpose of this study was to prepare and characterize nimodipine loaded microspheres using ethyl cellulose (ec) as a carrier polymer through an emulsion solvent evaporation method. these evaluations characterized the pattern of drug release from prepared microspheres. nimodipin loaded microspheres were prepared using an emulsification solvent evaporation method. the effect of process variab...

Journal: :iranian journal of pharmaceutical sciences 0
muhammad imran faculty of pharmacy, bhauddin zakaryia university, multan, pakistan. nazar muhammad ranjha faculty of pharmacy, bhauddin zakaryia university, multan, pakistan. rao khurram ayoub faculty of pharmacy, bhauddin zakaryia university, multan, pakistan.

the main objective of the present study was to formulate gastroretentive effervescent sustained release drug delivery systems of risperidone floating tablets with the help of methocel® k15, ethocel® standard 7fp premium, eudragit ® rs100 sustained release polymers to improve its safety profile, bioavailability and patient compliance. risperidone floating tablets were formulated by wet granulati...

H Valizadeh J Akbari K Morteza-Semnani M Saeedi M Tahernia R Enayatifard

The aim of this study was to develop an extended-release tablet formulation using a new in situ cross-linking method. The effects of polyvalent cations on theophylline release from tablets made with the polyanionic polymers sodium alginate and sodium carboxymethylcellulose, were investigated. Different miliequivalents of the di and tri-valent cation, Ca2+ and Al3+, were added to tablet form...

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