نتایج جستجو برای: among powder formulations

تعداد نتایج: 1234364  

2013
Natalie Glube Lea von Moos Guus Duchateau

PURPOSE In vitro disintegration and dissolution are routine methods used to assess the performance and quality of oral dosage forms. The purpose of the current work was to determine the potential for interaction between capsule shell material and a green tea extract and the impact it can have on the release. METHODS A green tea extract was formulated into simple powder-in-capsule formulations...

Journal: :Jurnal farmasi sains dan praktis 2022

The main components for tablet formulations are the fillers, binders, crushers, thinners and lubricants. Among these components, binders play a key role on powder cohesion properties during formation of granules. In this study, turmeric extract tablets were formulated using 15 g extract, 35 aerosil, 12.8 lactose, 1% magnesium stearate, 200 ml aquadest gelatin as binder. To evaluate effect formu...

2013
Sergey V. Dorozhkin

In early 1980s, researchers discovered self-setting calcium orthophosphate cements, which are bioactive and biodegradable grafting bioceramics in the form of a powder and a liquid. After mixing, both phases form pastes, which set and harden forming either a non-stoichiometric calcium deficient hydroxyapatite or brushite. Since both of them are remarkably biocompartible, bioresorbable and osteoc...

اکبری , جعفر, سررشته دار , شیرین, سعیدی , مجید, عنایتی فرد , رضا,

Background and purpose: The increasing effect of liquisolid systems on dissolution behavior of poor soluble drugs has been proved. In this research, the effect of glycerin, as a nonvolatile solvent, on release profile of indomethacin was evaluated. Materials and methods: The Avicel as carrier and silica as coating powder material in 20: 1 ratio were used. Indomethacin was dispersed in glyc...

2009

SUMMARY Roller compacted hydrophilic polymer combinations were used to formulate verapamil hydrochloride (HCl) extended release hydrophilic matrix tablets. The effect of roller compaction (RC) parameters on the properties of blended polymers, tablets and drug release were investigated. RC granulation improved the powder properties without affecting the pharmacotechnical properties or the drug r...

2014
Supriya Patil Vinit Patil Amol Shete Rajendra Doijad

The objectives of present investigations were to optimize concentration of oil, surfactant and cosurfactant by pseudoternary phase diagrams and to develop a stable formulation of self emulsifying drug delivery system (SEDDS) in order to enhance the dissolution rate of poorly soluble Irbesartan (IBS) by SEDDS. Pseudoternary phase diagrams were constructed to identify the self emulsifying region....

Journal: :International journal of pharmaceutics 2010
M Sherry Ku Weiyi Li Wendy Dulin Fran Donahue Dominique Cade Hassan Benameur Keith Hutchison

This Part I paper describes the qualification of a new high performance hypromellose (hydroxypropyl methylcellulose, HPMC) capsule shell which contains no gelling agent and is dissolution friendly. The development history and the test results for a series of quality attributes including scanning electron microscopy, hygroscopicity, machineability, weight variation, powder leakage, mechanical st...

2014
Sabera Khatun Kumar B. Sutradhar

In recent years natural polymers have been widely used because of their effectiveness and availability over synthetic polymers. In this present investigation matrix tablets of Metformin hydrochloride were formulated using Water hyacinth powder and its rate retardant activity was studied. Tablets were prepared using wet granulation method with 8% starch as granulating agent and 5, 10, 15, 20, 25...

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