نتایج جستجو برای: release efficiency

تعداد نتایج: 594837  

Bizhan Malaekeh-Nikouei Mahmoud R. Jaafari Nigel M. Davies Sayyed A. Sajadi Tabassi,

        The purpose of this study was to prepare and characterize microspheres loaded by cyclosporine A(CyA)-cyclodextrin (CD) complex. To achieve this goal, PLGA microspheres loaded by CyA CD complex were prepared by multiple emulsificationsolvent evaporation methods.Morphology, size, encapsulation efficiency and drug release from these microspheres were evaluated. Microscopic evaluation of mi...

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...

Thymol, an important and advantageous component of many essential oils, has been applied as an antimicrobial agent in animals. To increase the duration of action of this compound in ruminants, it was decided here to prepare a controlled release carrier for thymol. Hydroxy propyl methyl cellulose (HPMC) and ethyl cellulose (EC) were used as the matrix polymer here. Mixtures of thymol with eight ...

Journal: :jundishapur journal of natural pharmaceutical products 0
masoud ali karami school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran behzad sharif makhmal zadeh school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; nanotechnology research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran maryam koochak school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran eskandar moghimipur school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

conclusions the results indicated that sod-loaded in sln was delivered into deep burned skin layer and induced high enzyme activity through the skin. low particle size, application of lecithin as surfactant and low crystallinity index (ci) percentage were important factors for increasing sod penetration through the burned rat skin. percentage of activity by sln dispersions through rat skin was ...

Thymol, an important and advantageous component of many essential oils, has been applied as an antimicrobial agent in animals. To increase the duration of action of this compound in ruminants, it was decided here to prepare a controlled release carrier for thymol. Hydroxy propyl methyl cellulose (HPMC) and ethyl cellulose (EC) were used as the matrix polymer here. Mixtures of thymol with eight ...

Background: Eptifibatide (Integrilin) is an intravenous (IV) peptide drug that selectively inhibits ligand binding to the platelet GP IIb/IIIa receptor. It is an efficient peptide drug, however has a short half-life. Therefore, antithrombotic agents like eptifibatide are required to become improved with a protected and targeted delivery system such as using nano-liposomes to the site of thrombu...

Journal: :iranian journal of pharmaceutical research 0
mitra jelvehgari department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, iran. drug applied reseach center, tabriz university of medical sciences, tabriz, iran. davoud hassanzadeh department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, iran. drug applied research center, tabriz university of medical sciences, tabriz, iran. farhad kiafar department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, iran. badir delf loveymi department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, iran. sara amiri department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, iran.

the objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic acid (ma) using two polymers with different characteristics as ethylcellulose (ec) and/or cellulose acetate phthalate (cap). microspheres were prepared by the modified emulsion solvent evaporation (mese). the effect of drug-polymer interaction was studied for each of microspheres. important param...

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 ...

Journal: :pharmaceutical and biomedical research 0
abdesh singh department of pharmaceutics, rajiv academy for pharmacy, mathura, u.p, india manish kumar department of pharmaceutics, rajiv academy for pharmacy, mathura, u.p, india kamla pathak department of pharmaceutics, rajiv academy for pharmacy, mathura, u.p, india

the present investigation was aimed at developing a novel colon targeted system of lornoxicam based on the use of a combination of ph dependent system (to prevent the premature release of drug in the upper git) and enzymatically degradation system (to ensure the specificity of drug release in the colon). the drug loaded guar gum microspheres prepared by emulsification cross-linking method were ...

As encapsulation of hydrophilic drugs in the solid lipid nanoparticles (SLNs) is still a challenging issue, the aim of this study was to prepare SLNs containing tramadol hydrochloride as a hydrophilic compound.The SLNs were prepared using glycerol monostearate (GMS), soy lecithin and tween 80 by double emulsification-solvent evaporation technique. The nanoparticles were optimized through a cent...

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