نتایج جستجو برای: drug release profile

تعداد نتایج: 973228  

Journal: :iranian journal of pharmaceutical sciences 0
saini nish school of pharmaceutical sciences, shoolini university solan (h.p), india george mathew school of pharmaceutical sciences, shoolini university solan (h.p), india joseph lincy school of pharmaceutical sciences, shoolini university solan (h.p), india

the purpose of this review article is to characterize all of the parameters regarding the types, polymers used, and release kinetics of matrix tablets. matrix system was the earliest oral extended release platform for medicinal use. matrix tablets are most commonly used methods to modulate the release profile of drugs. they are much desirable and preferred for such therapy because they offer be...

A Shakeri-Zadeh, J Beik, M B Shiran, S Khoee S Khoei Z Abed,

Background: Drug nano-carriers are one of the most important tools for targeted cancer therapy so that undesired side effects of chemotherapy drugs are minimized. In this area, the use of ultrasound can be helpful in controlling drug release from nanoparticles to achieve higher treatment efficiency.Objective: Here, we studies the effects of ultrasound irradiation on the release profile of 5-flu...

Journal: :journal of biomedical physics and engineering 0
z abed 1medical physics department, school of medicine, tehran university of medical sciences (tums), tehran, iran j beik medical physics department, school of medicine, iran university of medical sciences (iums), tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) s khoee polymer chemistry department, school of sciences, university of tehran, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) s khoei medical physics department, school of medicine, iran university of medical sciences (iums), tehran, iranسازمان اصلی تایید شده: دانشگاه تهران (tehran university) a shakeri-zadeh medical physics department, school of medicine, iran university of medical sciences (iums), tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) m b shiran medical physics department, school of medicine, iran university of medical sciences (iums), tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

background: drug nano-carriers are one of the most important tools for targeted cancer therapy so that undesired side effects of chemotherapy drugs are minimized. in this area, the use of ultrasound can be helpful in controlling drug release from nanoparticles to achieve higher treatment efficiency. objective: here, we studies the effects of ultrasound irradiation on the release profile of 5-fl...

H Rahman MS Islam S Reza

Extended-release matrix tablets of diltiazem hydrochloride (DTZ) were prepared using waxy materials alone or in combination with Kollidon SR. Matrix waxy materials were carnauba wax (CW), bees wax (BW), cetyl alcohol (CA) and glyceryl monostearate (GMS). Dissolution studies were carried out by using a six stations USP XXII type 1 apparatus. The in vitro drug release study was done in 1000 ml ph...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه رازی - دانشکده علوم 1389

here, we report analysis of in vitro and in vivo drug release from an in situ formulation consisting of triamcinolone acetonide (tr) and poly(d,l-lactide-co-glycolide) (plga) and the additives glycofurol and hydroxyapatite nanoparticles (ha). we found that these additives enhanced drug release rate. we used the taguchi method to predict optimum formulation variables to minimise the initial burs...

H Rahman MS Islam S Reza

Extended-release matrix tablets of diltiazem hydrochloride (DTZ) were prepared using waxy materials alone or in combination with Kollidon SR. Matrix waxy materials were carnauba wax (CW), bees wax (BW), cetyl alcohol (CA) and glyceryl monostearate (GMS). Dissolution studies were carried out by using a six stations USP XXII type 1 apparatus. The in vitro drug release study was done in 1000 ml ph...

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 ...

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. ...

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. ...

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