نتایج جستجو برای: floating drug delivery system

تعداد نتایج: 2866942  

2014
Upendra Nagaich Vandana Chaudhary Jaya Nagaich Neha Gulati S. D. Tonpay

Gastroretentive drug delivery system i.e. floating microspheres of an H2 receptor antagonist drug ‘famotidine’ was successfully prepared using combination of polymer as hydroxyl propyl ethyl cellulose K15M (HPMC K15M) and cellulose acetate via non-aqueous solvent evaporation (oil-in-water) technique. Famotidine loaded floating microsphere formulations were prepared by dissolving polymer in solv...

2004
Mukesh C. Gohel Pavak R. Mehta Rikita K. Dave Nehal H. Bariya

Introduction A modified release drug delivery system with prolonged residence time in the stomach is of particular interest for drugs: (a) that are locally acting in the stomach, (b) that have an absorption window in the stomach or in the upper part of small intestine, (c) that are unstable in the intestinal or colonic environments, or (d) have low solubility at high pH values. Systems that pro...

2012
Furquan Nazimuddin Khan Mohamed Hassan G. Dehghan

Atorvastatin calcium, a lipid-lowering drug, is much less bioavailable because of reduced solubility in acidic media. Multiple-unit floating microcapsules of Atorvastatin calcium (ATC) were developed to expand the gastric residence time of the drug, as ATC has maximum rate of absorption in the upper GI tract. Floating microcapsules were prepared by Emulsion-solvent evaporation technique through...

Journal: :iranian journal of pharmaceutical research 0
f atyabi r vahabzadeh r dinarvand

in the long-term management of ulcerative colitis patients, repeat dosing maybe required. since 5-asa is largely absorbed from the upper intestine, selective delivery of drugs into the colon may be regarded as a better method of drug delivery with fewer side effects and a higher efficacy. the aim of this study was to prepare and evaluate a double coated multiparticulate system for 5-asa deliver...

2014
Swati C. Jagdale Vishnu M. Suryawanshi Sudhir V. Pandya Bhanudas S. Kuchekar Aniruddha R. Chabukswar

Lisinopril is an angiotensin-converting enzyme (ACE) inhibitor, primarily used for the treatment of hypertension, congestive heart failure, and heart attack. It belongs to BCS class III having a half-life of 12 hrs and 25% bioavailability. The purpose of the present work was to develop a press-coated, floating-pulsatile drug delivery system. The core tablet was formulated using the super-disint...

Journal: :Journal of Drug Delivery Science and Technology 2021

In this study, we developed a simple and easy method to use bicarbonate buffer solutions for dissolution tests. A floating lid was newly introduced prevent the evaporation of CO2 from (the method). This used evaluate profiles 5-aminosalicylic acid (5-ASA) colonic delivery tablets with pH-sensitive film coating (5-ASA CDT) (Asacol® 400 mg tablet generic products B). sodium solution added test ve...

Journal: :Asian Journal of Pharmaceutical and Clinical Research 2021

Objective: The aim of this study was to design and optimize lipid based beads for multiunit floating drug delivery ramipril.
 Methods: prepared by melt-solidification method. In the investigation 32 full factorial used investigate joint influence two formulation variable amount Gelucire (X1) Tween 20 (X2) as independent percentage release in 1 (Y1), 6 (Y2), 12 h (Y3) dependent variable. 43...

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