نتایج جستجو برای: release matrix tablet

تعداد نتایج: 594442  

Abdesh Singh, Kamla Pathak, Manish Kumar,

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 ...

Drug delivery via buccal mucosa by means of buccoadhesive formulations offer distinct advantages over peroral administration. Recently, plant gums and exudates have been screened for their use as pharmaceutical adjuvants. The aim of this study is to evaluate matrix tablets containing Plantago psyllium seed mucilage in addition to carbopol as a mucoadhesive agent, and propranolol hydrochloride a...

Journal: :iranian journal of pharmaceutical sciences 0
majid saeedi department of pharmaceutics, faculty of pharmacy, mazandaran university of medical sciences jafar akbari department of pharmaceutics, faculty of pharmacy, mazandaran university of medical sciences, sari, iran. katayoun morteza-semnani department of medicinal chemistry, faculty of pharmacy, mazandaran university of medical sciences, sari, iran ali azarashk department of pharmaceutics, faculty of pharmacy, mazandaran university of medical sciences, sari, iran.

drug delivery via buccal mucosa by means of buccoadhesive formulations offer distinct advantages over peroral administration. recently, plant gums and exudates have been screened for their use as pharmaceutical adjuvants. the aim of this study is to evaluate matrix tablets containing plantago psyllium seed mucilage in addition to carbopol as a mucoadhesive agent, and propranolol hydrochloride a...

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...

2010
E. I. Nep B. R. Conway

Matrix-based tablets using 40 %w/w grewia gum were prepared by direct compression to contain cimetidine as novel drug. The formulations were compared with similar formulations using hydroxypropyl methylcelluose (Methocel), gum arabic, carboxy methylcellulose (Blanose), or ethyl cellulose (Ethocel) as polymer matrix. Also binary composite matrices containing grewia gum and the reference polymers...

Journal: :iranian journal of pharmaceutical research 0
seyed alireza mortazavi department of pharmaceutics, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. yasaman ghadjahani pharmaceutical sciences branch islamic azad university, tehran, iran hoda mahmoodi pharmaceutical sciences branch islamic azad university, tehran, iran farzaneh mehtarpour pharmaceutical sciences branch islamic azad university, tehran, iran zahra jaffariazar pharmaceutical sciences branch islamic azad university, tehran, iran

the purpose of this study was preparation and evaluation of sustained release matrix type ocular mini-tablets of timolol maleate, as a potential formulation for the treatment of glaucoma. following the initial studies on timolol maleate powder, it was formulated into ocular mini-tablets. the polymers investigated in this study included cellulose derivatives (hec, cmc, ec) and carbopol971p. mann...

Journal: :The Journal of pharmacy and pharmacology 1999
T Dürig G M Venkatesh R Fassihi

The effects of the amounts of lubricants (magnesium stearate 0-5% and talc 0-3%) and changes in compaction rate and tablet porosity on the mechanism of drug release from high drug-load controlled-release theophylline tablets have been examined. Drug release was satisfactorily described by a surface-erosion model that takes into account the geometry of the tablet, differential radial and axial e...

Journal: :Drug Delivery 2009
Nahla S. Barakat Ibrahim M. Elbagory Alanood S. Almurshedi

The objective of this study was to investigate the effect of lipophilic (Compritol 888 ATO) and hydrophilic components (combination of HPMC and Avicel) on the release of carbamazepine from granules and corresponding tablet. Wet granulation followed by compression was employed for preparation of granules and tablets. The matrix swelling behavior was investigated. The dissolution profiles of each...

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