Results 41 to 50 of about 346 (137)

Formulation and In-Vitro Evaluation of Darifenacin Hydrobromide as Buccal Films

open access: yesIraqi Journal of Pharmaceutical Sciences, 2019
Darifenacin hydrobromide (DH) is the more recent uroselective M3 receptor antagonist for treating uncomplicated overactive bladder (OAB). This study was aimed to formulate DH as fast dissolving buccal films (FDBFs) using a solvent casting method to ...
Ishraq k. Abbas   +2 more
doaj   +1 more source

Improvement of Meloxicam Solubility Using a β-Cyclodextrin Complex Prepared via the Kneading Method and Incorporated into an Orally Disintegrating Tablet [PDF]

open access: yesAdvanced Pharmaceutical Bulletin, 2016
Purpose: The aim of this research was to formulate and develop an orally disintegrating tablet (ODT) that incorporated a MEL/β-CD complex, using a quality by design (QbD) approach to enhance solubility and drug release.
Ahmad Ainurofiq   +6 more
doaj   +1 more source

The effects of croscarmellose sodium concentration on the physicochemical characteristics of orodispersible tablets of atenolol [PDF]

open access: yesPharmaciana, 2018
Hypertension is the most common cardiovascular diseases suffered by geriatric patients. Their physiological changes make the administration of conventional tablets less effective, especially regarding compliance.
Nani Parfati, Karina Citra Rani
doaj   +1 more source

Development of fast dispersible aceclofenac tablets: Effect of functionality of superdisintegrants

open access: yesIndian Journal of Pharmaceutical Sciences, 2008
Aceclofenac, a non-steroidal antiinflammatory drug, is used for posttraumatic pain and rheumatoid arthritis. Aceclofenac fast-dispersible tablets have been prepared by direct compression method. Effect of superdisintegrants (such as, croscarmellose sodium, sodium starch glycolate and crospovidone) on wetting time, disintegration time, drug content, in ...
Setty, C. Mallikarjuna   +3 more
openaire   +3 more sources

Synthesis of MCC–PEG Conjugate and Its Evaluation as a Superdisintegrant [PDF]

open access: yesAAPS PharmSciTech, 2010
PEGylated conjugate of microcrystalline cellulose (MCC) was synthesized by reacting MCC with polyethylene glycol (PEG) 200 in the presence of catalyst at elevated temperature. Conjugation between MCC and PEG was confirmed by FT-IR and (1)H NMR studies.
Mangesh R, Bhalekar   +2 more
openaire   +2 more sources

Oligohydramnios and fetal outcome in term pregnancy

open access: yesZanco Journal of Medical Sciences, 2020
Background and objective: Orally disintegrating film is a solid dosage form made as an alternative for tablets for pediatric and geriatric patients who have difficulty in swallowing.
Hazha Azad Ibrahim, Zainab Muhsin Zween
doaj   +1 more source

Development and optimization of dispersible tablet of Bacopa monnieri with improved functionality for memory enhancement

open access: yesJournal of Pharmacy and Bioallied Sciences, 2017
Introduction: The Bacopa monnieri is traditional Ayurvedic medicine, and reported for memory-enhancing effects. The Bacoside is poorly soluble, bitter in taste and responsible for the memory enhancement action.
Vaishali Tejas Thakkar   +7 more
doaj   +1 more source

Formulation of a fast-dissolving oral film using gelatin and sodium carboxymethyl cellulose

open access: yesZanco Journal of Medical Sciences, 2020
Background and objective: Orally disintegrating film is a solid dosage form made as an alternative for tablets for pediatric and geriatric patients who have difficulty in swallowing.
Jwan Mohammed Ahmed   +2 more
doaj   +1 more source

Formulation and Optimization of Oral Fast Dissolving

open access: yesIraqi Journal of Pharmaceutical Sciences, 2017
Prochloperazine maleate (PCM) is one of the most prescribed phenothiazine. The purpose of the present research was to develop fast dissolving tablets of PCM with β-cyclodextrin inclusion complex. Tablets prepared  by wet granulation with sublimation and
Dua'a K. Ahmed, Balkis A. Kamal
doaj  

Preparation and characterization of timed drug delivery system of sumatriptan using natural polymers

open access: yesIraqi Journal of Pharmaceutical Sciences, 2018
Pulsatile drug delivery systems are time-controlled dosage forms which are designed to release the active pharmaceutical ingredient after a predetermined lag time to synchronize the disease circadian rhythm.
Mina Shihab Al-anbagi   +2 more
doaj   +1 more source

Home - About - Disclaimer - Privacy