1 US Pharmacopoeia National Formulary, "USP 26-NF21" Mack Printing Company 2439-, 2003
2 Shep, S., "Swelling system:a novel approach towards gastroretentive drug delivery system" 1 : 234-242, 2011
3 Serajuddin, A. T. M., "Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs" 88 : 1058-1066, 1999
4 Fouladi, F., "Preparation and in vitro evaluation of gastroretensive Bupropion hydrochloride tablets" 11 : 351-359, 2012
5 Saito, N., "Plural transformation-processes from spiral to coccoid Helicobacter pylori and its viability" 46 : 49-55, 2003
6 Baboota, S., "Physicochemical characterization, in vitro dissolution behavior, and pharmacodynamic studies of Rofecoxib-cyclodextrin inclusion compounds. Preparation and properties of Rofecoxib hydroxypropyl β-cyclodextrin inclusion complex: A technical note" 6 : 83-90, 2005
7 Siepmann, J., "Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose" 48 : 139-157, 2001
8 Xu, W. J., "In vitro dissolution and physicochemical characterizations of novel PVPbased solid dispersion containing valsartan prepared by a freezedrying method" 27 : 1799-1804, 2014
9 Ministry of Food and Drug Safety, "Guideline on validation of analytical procedure"
10 Kadivar, A., "Formulation and in vitro, in vivo evaluation of effervescent floating sustained release imatinib mesylate tablet" 10 : e0126874-, 2015
1 US Pharmacopoeia National Formulary, "USP 26-NF21" Mack Printing Company 2439-, 2003
2 Shep, S., "Swelling system:a novel approach towards gastroretentive drug delivery system" 1 : 234-242, 2011
3 Serajuddin, A. T. M., "Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs" 88 : 1058-1066, 1999
4 Fouladi, F., "Preparation and in vitro evaluation of gastroretensive Bupropion hydrochloride tablets" 11 : 351-359, 2012
5 Saito, N., "Plural transformation-processes from spiral to coccoid Helicobacter pylori and its viability" 46 : 49-55, 2003
6 Baboota, S., "Physicochemical characterization, in vitro dissolution behavior, and pharmacodynamic studies of Rofecoxib-cyclodextrin inclusion compounds. Preparation and properties of Rofecoxib hydroxypropyl β-cyclodextrin inclusion complex: A technical note" 6 : 83-90, 2005
7 Siepmann, J., "Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose" 48 : 139-157, 2001
8 Xu, W. J., "In vitro dissolution and physicochemical characterizations of novel PVPbased solid dispersion containing valsartan prepared by a freezedrying method" 27 : 1799-1804, 2014
9 Ministry of Food and Drug Safety, "Guideline on validation of analytical procedure"
10 Kadivar, A., "Formulation and in vitro, in vivo evaluation of effervescent floating sustained release imatinib mesylate tablet" 10 : e0126874-, 2015
11 Solanki, N. D., "Formulation and evaluation of once a day bilayer floating tablet of antihypertensive drug involving dissolution enhancement approach" 4 : 54-66, 2013
12 Patel, D. M., "Formulation and evaluation of mixed matrix gastro-retentive drug delivery for famotidine" 1 : 247-254, 2011
13 Sharma, N., "Formulation and evaluation of gastric retensive floating tablets containing Cefpodoxime proxetil solid dispersions" 4 : 82-87, 2012
14 Hingmire, L. P., "Formulation and evaluation of Valsartan SR tablets using hydrophilic and hydrophobic polymer" 6 : 254-260, 2013
15 Singh, B. N., "Floating drug delivery systems:An approach to oral controlled drug delivery via gastric retention" 63 : 235-259, 2000
16 Arora, S., "Floating drug delivery systems: A review" 6 : 372-390, 2005
17 Vervaet C., "Extrusion-spheronization:A literature review" 116 : 131-146, 1995
18 Cockburn, J., "Effects of intervention on antibiotic compliance in patients in general practice" 147 : 324-328, 1987
19 Mamajek, R. C., "Drug-dispensing device and method"
20 Urquhart, J., "Drug delivery system comprising a reservoir containing a plurality of tiny pills"
21 Bechgaard, H., "Distribution of pellets in the gastrointestinal tract. The influence on transit time exerted by the density or diameter of pellets" 30 : 690-692, 1978
22 Ha, N. S., "Dissolution-enhancing mechanism of alkalizers in poloxamer-based solid dispersions and physical mixtures containing poorly watersoluble valsartan" 59 : 844-880, 2011
23 Chen, R. N., "Development of swelling / floating gastroretensive drug delivery system based on a combination of hydroxyethyl cellulose and sodium carboxymethyl cellulose for Losartan and its clinical relevance in healthy volunteers with CYP2C9 polymorphism" 39 : 82-89, 2010
24 Kumar, N., "Development and optimization of gastroretentive controlled-release tablet of calcium-disodium edetate and its in vivo gamma scintigraphic evaluation" 16 : 1270-1280, 2015
25 Talegaonikar, S., "Development and characterization of Paracetamol complexes with hydroxypropyl β-cyclodextrin" 6 : 95-99, 2007
26 Chitnis, V. S., "Bioadhesive polymers-synthesis, evaluation and application in controlled release tablets" 17 : 879-892, 1991
27 Park, K. N., "Bioadhesive polymers as platforms for oral-controlled drug delivery: method to study bioadhesion" 19 : 107-127, 1984
28 Ritger, P. L., "A simple equation for description of solute release II. Fickian and anomalous release from swellable devices" 5 : 37-42, 1987