نتایج جستجو برای: in vitro drug release

تعداد نتایج: 17076627  

Journal: :jundishapur journal of natural pharmaceutical products 0
abbas akhgari nanotechnology research center and school of pharmacy, ahvaz jundishapur university of medical sciences, tel./fax: +98-6113738381, ir iran mohammadreza abbaspour nanotechnology research center and school of pharmacy, ahvaz jundishapur university of medical sciences, tel./fax: +98-6113738381, ir iran ; nanotechnology research center and school of pharmacy, ahvaz jundishapur university of medical sciences, tel./fax: +98-6113738381, ir iran meysam moradkhanizadeh nanotechnology research center and school of pharmacy, ahvaz jundishapur university of medical sciences, tel./fax: +98-6113738381, ir iran

conclusions it was shown that combination of pectin and eudragits can relatively control drug release in the upper gi. on the other hand, pectin degraded in the presence of pectinase and formulations were susceptible to the colonic media. results it was shown that in the presence of pectin, formulations without erl had a relative resistance to drug release in sgf. pellets containing pectin and ...

Journal: :international journal of nano dimension 0
p. srinivas department of pharmaceutics, sri venkateshwara college of pharmacy & research centre, affiliated to osmania university, hyderabad, india. t. sumapriya department of pharmaceutics, sri venkateshwara college of pharmacy & research centre, affiliated to osmania university, hyderabad, india.

the aim of the present study was to develop exemestane loaded polymeric nanoparticles for improved oral bioavailability of exemestane. exemestane loaded nanoparticles were prepared by solvent displacement method with eudragit rl 100 and eudragit l 100 as polymers and pluronic® f-68 as surfactant. the influence of various formulation factors (drug: polymer ratio and concentration of surfactant) ...

P. Srinivas, S. Pragna

The objective of the present study was to prepare controlled release formulation of Moxifloxacin hydrochloride ocular nanoparticles. The nanoparticles were prepared by solvent displacement method using Eudragit RL 100 as a polymer. Different formulations were prepared by varying the ratios of drug and polymer and varying the ratios of organic and aqueous phase. The formulations were evaluated i...

Inhalation delivery of aerosolized antibacterials is preferred over conventional methods of delivery for targeting lung infection. The present study is concerned with the development and characterization of a novel, spray dried, aerosolized, chitosan polyelectrolyte complex (PEC) based microparticles containing antibacterials for the treatment of lung infections.Chitosan polyelectrolyte complex...

Inhalation delivery of aerosolized antibacterials is preferred over conventional methods of delivery for targeting lung infection. The present study is concerned with the development and characterization of a novel, spray dried, aerosolized, chitosan polyelectrolyte complex (PEC) based microparticles containing antibacterials for the treatment of lung infections.Chitosan polyelectrolyte complex...

Golam Kibria, Monzurul Amin Roni Reza-ul Jalil

      Extended release formulation of alfuzosin, an a-antagonist used for prostatic hypertrophy, is available in market. It is convenient for older patients to take only one tablet a day. Marketed alfuzosin formulation is three layered geomatrix tablet that requires special facilities, high cost, more time and complex operation than normal direct compression formulation. Therefore, a less compl...

Silica aerogels are porous and extremely lightweight nano-materials shows interesting properties. These materials, because of biocompatibility, non-harmful to the body and special physical characteristics such as large surface area and low density have great potential for use in a drug delivery system (DDS). The focus of this study is the evaluation of the effects of silica aerogels on improvin...

Mitra Jelvehgari Nazila Derafshi Siavoush Dastmalch

Objective(s) The aim of this study was to formulate and evaluate microencapsulated controlled release preparations of theophylline using ethylcellulose as the retardant material with high entrapment efficiency. Materials and Methods Microspheres were prepared by water-in-oil-in-oil (W/O1/O2) emulsion-solvent diffusion (ESD). A mixed solvent system consisting of acetonitrile and dichloromet...

Journal: :nanomedicine journal 0
amir doustgani department of chemical engineering, university of zanjan, zanjan, iranسازمان اصلی تایید شده: دانشگاه زنجان (zanjan university)

objective(s): in this study, drug loaded electrospun nanofibrous mats were prepared and drug release and mechanism from prepared nanofibers were investigated.  materials and methods: paclitaxel (ptx) loaded polylactic acid (pla) nanofibers were prepared by electrospinning. the effects of process parameters, such as ptx concentration, tip to collector distance, voltage, temperature and flow rate...

A. Rezaei Mokarram H. Zolfagharian M.J. Alonso N. Mohammadpour Dounighi S.A. Mortazavi

  During last two decades, polysaccharides such as alginate (Alg) alone and in combination with other biopolymers are widely used in vaccine and drug delivery systems. The aim of the present work was to investigate the potential utility of microparticles made of alginate (Alg) as new vehicles for improving nasal vaccine delivery. For this purpose, diphtheria toxoid (DT) was chosen as a model an...

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