نتایج جستجو برای: vitro drug release

تعداد نتایج: 1119490  

Diclofenac sodium as ophthalmic dosage form is used in patients treatment of eye pain, swelling and redness recovering from cataract surgery but it faces the bioavailability limitation of eye drops due to effective protective mechanisms and corneal barrier functions in the eyes. Therefore, this investigation was aimed to develop ocular film formulations to achieve controlled drug release. Drug ...

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...

A Gadad A Kulkarni P Dandagi S Kerur V Mastiholimath

The aim of this study is to formulate a novel ophthalmic nanosuspension (ONS), an alternative carrier system to traditional colloidal carriers for controlled release (CR) of acyclovir (ACV). In the present study, ONS is employed to avoid some of major disadvantages of colloidal carriers systems such as instability in cul de sac and short half life by increasing efficiency of drug encapsulation ...

AS Kiran BS Ashok Kumar D Sheshadri Shaker KV Satish N Narayana Swamy N Suresh,

      An oral suspension could a suitable dosage form for the geriatric patients. The calcium alginate coated ion exchange resinate of propranolol hydrochloride were prepared using Amberlite IR-120 by solvent evaporation. Microcapsules of propranolol hydrochloride resinate were prepared by solvent evaporation technique,the suspensions were prepared by using deionised water as the vehicle. Methy...

The study aimed at determining the effect of acid modified porcine mucin powder on the release and permeation of insulin in transdermal patches. Various batches of insulin patches were prepared by solvent casting method using polysorbate 80 as emulsifying agent and acid treated and untreated mucin powders as base. The patches were evaluated for their physical properties, folding endurance, moi...

Abu Shara Shamsur Rouf Abul Kalam Lutful Kabir, Harun-Or- Rashid Md. Zakir Hossaina

     The purpose of this work was to develop once daily sustained release (SR) matrix tablets of naproxen, an anti-inflammatory agent. The tablets were prepared by wet granulation method along with hydrophilic matrix materials like Methocel K 15M CR and Methocel K 100M CR. The granules were evaluated for bulk density, angle of repose, compressibility index, total porosity and drug content. The ...

Diclofenac sodium as ophthalmic dosage form is used in patients treatment of eye pain, swelling and redness recovering from cataract surgery but it faces the bioavailability limitation of eye drops due to effective protective mechanisms and corneal barrier functions in the eyes. Therefore, this investigation was aimed to develop ocular film formulations to achieve controlled drug release. Drug ...

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: :research in pharmaceutical sciences 0
sara salatin 1research center for pharmaceutical nanotechnology, tabriz university of medical science, tabriz, i.r. iran. 2student research committee, tabriz university of medical science, tabriz, i.r. iran. jaleh barar 1research center for pharmaceutical nanotechnology, tabriz university of medical science, tabriz, i.r. iran. 3department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, i.r. iran. mohammad barzegar-jalali 3department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, i.r. iran. khosro adibkia 3department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, i.r. iran. 4drug applied research center and faculty of pharmacy, tabriz university of medical sciences, tabriz, i.r. iran. farhad kiafar 3department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, i.r. iran. 5zahravi pharmaceutical company, tabriz, i.r. iran. mitra jelvehgari 3department of pharmaceutics, faculty of pharmacy, tabriz university of medical sciences, tabriz, i.r. iran. 4drug applied research center and faculty of pharmacy, tabriz university of medical sciences, tabriz, i.r. iran.

rivastigmine hydrogen tartrate (rht), one of the potential cholinesterase inhibitors, has received great attention as a new drug candidate for the treatment of alzheimer's disease. however, the bioavailability of rht from the conventional pharmaceutical forms is low because of the presence of the blood brain barrier. the main aim of the present study was to prepare positively charged eudragit r...

Journal: :iranian journal of pharmaceutical research 0
pankaj kumar soa university, bhubneshwar, orissa, india ashok laxmanrao ganure sahyadri college of pharmacy, sangola, solapur, india bharat bhusan subudhi school of pharmaceutical sciences, siksha o anusandhan university, bhubaneswar, india shubhanjali shukla department of pharmaceutics, indian institute of technology (banaras hindu university), varanasi, india

the present investigation deals with the development of controlled release tablets of salbutamol sulphate using graft copolymers (st-g-pmma and ast-g-pmma) of starch and acetylated starch. drug excipient compatibility was spectroscopically analyzed via ft-ir, which confirmed no interaction between drug and other excipients. formulations were evaluated for physical characteristics like hardness,...

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