نتایج جستجو برای: release

تعداد نتایج: 214420  

HR Patel MM Patel

The aim of the present study was to prepare and evaluate an osmotically controlled mucoadhesive cup-core (OCMC) containing aceclofenac. A special technique was used while preparing an OCMC. Stability of OCMC was determined in natural human saliva, and it was found that both pH and device are stable in human saliva. OCMC was evaluated by weight uniformity, thickness, hardness, friability, swelli...

Fatemeh Pourhashem Mohammad Reza Avadi

The goal of this study was to design and evaluate extended - release system of the hypnotic agent, Zolpidemtartrate usefulness for the treatment of insomnia. The half-life of this drug is about 1.9 - 3 hours that indicatingit a candidate for the extended release formulation. Our investigation relates to development of extendeddrug delivery system based on Hydroxy propyl methyl cellulose (HPMCK4...

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,...

H Mehrgan SA Mortazavi

In this study, the effects of various hydrophilic (HPMC and Carbopol 971) and plastic (Ethylcellulose and Eudragit RL100) polymers on the release profile of diltiazem HCl from matrix tablets were evaluated in-vitro. For this purpose, tablets containing 60 mg of diltiazem HCl along with various amounts of the aforementioned polymers were prepared using the wet granulation technique. Tablets prep...

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,...

Journal: :iranian journal of basic medical sciences 0
shulai zhou children’s hospital, zhejiang university school of medicine, hangzhou, zhejiang, 310003 china lichao gao children’s hospital, zhejiang university school of medicine, hangzhou, zhejiang, 310003 china fangqi gong children’s hospital, zhejiang university school of medicine, hangzhou, zhejiang, 310003 china xiaoyang chen children’s hospital, zhejiang university school of medicine, hangzhou, zhejiang, 310003 china

objective(s): this study was designed to investigate the effect of receptor for advanced glycation end products (rage), s100a12 and c-reactive protein (crp) on the release of circulating endothelial cells (cecs) from human coronary artery endothelial cells (hcaecs). materials and methods: hcaecs were cultured in increasing concentration of crp (0, 12.5, 25, 50μg/ml) or s100a12 protein (0, 4, 10...

Journal: :iranian journal of pharmaceutical sciences 0
golnar dorraj department of pharmaceutics and nanotechnology, school of pharmacy, shahid beheshti university of medical sciences, po box: 14155-6153, tehran, iran. hamid r. moghimi department of pharmaceutics and nanotechnology, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. pharmaceutical sciences research center, shahid beheshti university of medical sciences, tehran, iran.

preparation and characterization of thermoresponsive in-situ forming poloxamer hydrogel for controlled release of nile red-loaded solid lipid nanoparticles. nanoparticles (nps) are cleared rapidly from systemic circulation and do not provide sustained action in most cases. to solve this problem, this investigation introduces an erodible in-situ forming gel system as potential vehicles for prolo...

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...

Journal: :iranian journal of pharmaceutical research 0
a attar nasseri r aboofazeli t needham t needham

ketorolac tromethamine (kt) containing microemulsion-based gels (mbgs) have been formulated, based on the previous phase diagram studies, using a pharmaceutically acceptable surfactant (soybean lecithin; epikuron 200) and oil (isopropyl myristate; ipm) and the effect of formulation variables on the release profile of the drug from mbgs through intact guinea pig skin and various artificial membr...

Journal: :iranian journal of pharmaceutical sciences 0
mohammad mehdi mahboobian department of pharmaceutics, school of pharmacy and protein technology research center , shahid beheshti university of medical sciences, tehran, iran. seyed mohsen foroutan department of pharmaceutics, school of pharmacy and protein technology research center , shahid beheshti university of medical sciences, tehran, iran. reza aboofazeli department of pharmaceutics, school of pharmacy and protein technology research center , shahid beheshti university of medical sciences, tehran, iran.

the aim of this investigation was to design and develop nanoemulsions (nes) as novel ophthalmic delivery systems for brinzolamide (bzd). phase behavior of quaternary systems composed of triacetin and capryoltm 90 (selected oils, screened through the solubility studies), various surfactants (namely, cremophor rh 40, brij 35, labrasol and tyloxapol), transcutol p (as co-surfactant) and water a...

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