نتایج جستجو برای: fractional release profile

تعداد نتایج: 488099  

Journal: :iranian journal of pharmaceutical research 0
r dinarvand e rahmani e farbod

a topical o/w cream containing tretinoin microspheres was prepared. gelatin microspheres of tretinoin were prepared using coacervation method. these microspheres contained about 50% w/w tretinoin. the particle size range of microspheres was between 90-150 m m. in vitro drug release from microspheres and a cream formulation was studied. it was shown that drug release from microspheres followed h...

Journal: :Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 2009
Branka Ivić Svetlana Ibrić Gabriele Betz Zorica Djurić

The purpose of the study was to screen the effects of formulation factors on the in vitro release profile of diclofenac sodium from matrix pellets compressed into multiple unit pellet system (MUPS) tablets using design of experiment (DOE). Extended release of diclofenac sodium was accomplished using Carbopol 71G as matrix substance. According to Fractional Factorial Design FFD 2(3-1) four formu...

Journal: :iranian journal of pharmaceutical research 0
h tabandeh tb guilani

a sustained-release tablet formulation should ideally have a proper release profile insensitive to moderate changes in tablet hardness that is usually encountered in manufacturing. in this study, matrix aspirin (acetylsalicylic acid) tablets with ethylcellulose (ec), eudragit rs100 (rs), and eudragit s100 (s) were prepared by direct compression. the release behaviors were then studied in two co...

2013
Thekkethil Shefeeq Naseem Ahmad

An exact solution has been obtained for the release kinetics of a solute from a cylindrical non-erodible polymeric matrix into a finite external volume when the initial solute loading is greater than the solubility limit in the matrix. The moving boundary solution is derived based on the combination of variable method. The formulas of the moving boundary and the fractional solute release are gi...

Abstract The main aim of this study was to prepare and evaluate the extended - release system of an anxiolytic substance. Alprazolam is a short-acting benzodiazepine with general properties similar to those of diazepam. Our studies focused on the development of extended drug delivery system based on Hydroxy Propyl Methyl Cellulose (HPMC 4000cps) as retard agent and polyvinylpyrrolidone (PVP k30...

E Farbod E Rahmani R Dinarvand

A topical o/w cream containing tretinoin microspheres was prepared. Gelatin microspheres of tretinoin were prepared using coacervation method. These microspheres contained about 50% w/w tretinoin. The particle size range of microspheres was between 90-150 m m. In vitro drug release from microspheres and a cream formulation was studied. It was shown that drug release from microspheres followed H...

Journal: :iranian journal of veterinary medicine 0
sakineh khanamani falahatipour department of pharmacology, faculty of veterinary medicine, university of tehran, tehran, iran ali rasooli 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 associate prof. dept pharmaceutics, faculty of pharmacy, tehran university of medical sciences, tehran, iran. katayoun kiani dept pharmacology, faculty of vet med, university of tehran, tehran, iran. taghi zahraee salehi prof. and head of dept microbiology, faculty of vet med, university oftehran, tehran, iran.

background: the development of injectable sustained-release products are of great interest to veterinary pharmaceuticals and animal health business. recently, great attention has been paid to in situ gel-forming chitosan/beta-glycerophosphate (chitosan/β-gp) solutions due to their good biodegradability and thermosensitivity. objectives: the general aim of this study was to prepare a novel in si...

E Farbod E Rahmani R Dinarvand

A topical o/w cream containing tretinoin microspheres was prepared. Gelatin microspheres of tretinoin were prepared using coacervation method. These microspheres contained about 50% w/w tretinoin. The particle size range of microspheres was between 90-150 m m. In vitro drug release from microspheres and a cream formulation was studied. It was shown that drug release from microspheres followed H...

Journal: :iranian journal of pharmaceutical research 0
seyed alireza mortazavi department of pharmaceutics, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. sanaz pishrochi department of pharmaceutics, pharmaceutical sciences branch, islamic azad university, tehran, iran. zahra jafari azar department of pharmaceutics, pharmaceutical sciences branch, islamic azad university, tehran, iran.

in this study, tretinoin microemulsion has been formulated based on phase diagram studies by changing the amounts and proportions of inactive ingredients, such as surfactants, co-surfactants and oils. the effects of these variables have been determined on microemulsion formation, particle size of the dispersed phase and release profile of tretinoin from microemulsion through dialysis membrane. ...

Journal: :research in pharmaceutical sciences 0

alpha-1antitrypsin (a1at) deficiency, an inherited disorder, has been shown to be the cause of lung diseases such as emphysema and chronic obstructive pulmonary disease. one of the treatment strategies to provide appropriate and adequate concentrations of a1at in the lungsis the application of nanoparticles (nps) in pulmonary drug delivery. in the current study, biocompatible nanohydrogels were...

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