Drug release from E chemistry hypromellose tablets using the Bio-Dis USP type III apparatus: An evaluation of the effect of systematic agitation and ionic strength.

[1]  A. Nokhodchi,et al.  An assessment of triboelectrification effects on co-ground solid dispersions of carbamazepine , 2016 .

[2]  Waseem Kaialy,et al.  A review of factors affecting electrostatic charging of pharmaceuticals and adhesive mixtures for inhalation. , 2016, International journal of pharmaceutics.

[3]  Alan M. Smith,et al.  Development of mucoadhesive sprayable gellan gum fluid gels. , 2015, International journal of pharmaceutics.

[4]  A. Nokhodchi,et al.  Application of Polymer Combinations in Extended Release Hydrophilic Matrices , 2015 .

[5]  A. Nokhodchi,et al.  Agitation Sequence and Ionic Strength on In-Vitro Drug Release from Hypromellose –The Influence of Compaction Force , 2015 .

[6]  A. Nokhodchi,et al.  Triboelectrification and dissolution property enhancements of solid dispersions. , 2015, International journal of pharmaceutics.

[7]  I. Norton,et al.  The influence of co-solutes on tribology of agar fluid gels , 2015 .

[8]  Alan M. Smith,et al.  Evaluation of gellan gum fluid gels as modified release oral liquids. , 2014, International journal of pharmaceutics.

[9]  Ali Nokhodchi,et al.  Drug release from matrix tablets: physiological parameters and the effect of food , 2014, Expert opinion on drug delivery.

[10]  Waseem Kaialy,et al.  Psyllium: a promising polymer for sustained release formulations in combination with HPMC polymers , 2014, Pharmaceutical development and technology.

[11]  A. Nokhodchi,et al.  Towards a More Desirable Dry Powder Inhaler Formulation: Large Spray-Dried Mannitol Microspheres Outperform Small Microspheres , 2014, Pharmaceutical Research.

[12]  P. Panchmatia,et al.  The influence of salt formation on electrostatic and compression properties of flurbiprofen salts. , 2013, International journal of pharmaceutics.

[13]  Ali Nokhodchi,et al.  The effect of pH and ionic strength of dissolution media on in-vitro release of two model drugs of different solubilities from HPMC matrices. , 2013, Colloids and surfaces. B, Biointerfaces.

[14]  Waseem Kaialy,et al.  The influence of agitation sequence and ionic strength on in vitro drug release from hypromellose (E4M and K4M) ER matrices--the use of the USP III apparatus. , 2013, Colloids and surfaces. B, Biointerfaces.

[15]  A. Nokhodchi,et al.  Effect of glucosamine HCl on dissolution and solid state behaviours of piroxicam upon milling. , 2013, Colloids and surfaces. B, Biointerfaces.

[16]  A. Nokhodchi,et al.  The role of oral controlled release matrix tablets in drug delivery systems. , 2012, BioImpacts : BI.

[17]  M. Ghadiri,et al.  Tribo-electrification of active pharmaceutical ingredients and excipients , 2012 .

[18]  A. Nokhodchi,et al.  Release Behaviour of Propranolol HCl from Hydrophilic Matrix Tablets Containing Psyllium Powder in Combination with Hydrophilic Polymers , 2011, AAPS PharmSciTech.

[19]  Ali Nokhodchi,et al.  Effect of ionic strength and pH of dissolution media on theophylline release from hypromellose matrix tablets—Apparatus USP III, simulated fasted and fed conditions , 2011 .

[20]  R. Bushra,et al.  Food-drug interactions. , 2011, Oman medical journal.

[21]  Ali Nokhodchi,et al.  Study of dissolution hydrodynamic conditions versus drug release from hypromellose matrices: the influence of agitation sequence. , 2010, Colloids and surfaces. B, Biointerfaces.

[22]  M. Ghadiri,et al.  Analysis of a Simple Test Device for Tribo‐Electric Charging of Bulk Powders , 2009 .

[23]  R. Langer,et al.  Rheological blends for drug delivery. I. Characterization in vitro. , 2009, Journal of biomedical materials research. Part A.

[24]  P. Anzenbacher,et al.  Interactions of food and dietary supplements with drug metabolising cytochrome P450 enzymes. , 2007, Ceska a Slovenska farmacie : casopis Ceske farmaceuticke spolecnosti a Slovenske farmaceuticke spolecnosti.

[25]  D. Lacks,et al.  Effect of particle size distribution on the polarity of triboelectric charging in granular insulator systems , 2007 .

[26]  Kristl Julijana,et al.  Analysis of surface properties of cellulose ethers and drug release from their matrix tablets. , 2006, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[27]  A. Nokhodchi,et al.  The effect of hydrophilic and lipophilic polymers and fillers on the release rate of atenolol from HPMC matrices. , 2004, Farmaco.

[28]  O. Corrigan,et al.  Swelling and erosion properties of hydroxypropylmethylcellulose (Hypromellose) matrices--influence of agitation rate and dissolution medium composition. , 2004, International journal of pharmaceutics.

[29]  M. Tobyn,et al.  Influence of Physiological Variables on the In Vitro Drug-Release Behavior of a Polysaccharide Matrix Controlled-Release System , 2003, Drug development and industrial pharmacy.

[30]  S. Baumgartner,et al.  Investigation of the state and dynamics of water in hydrogels of cellulose ethers by1H NMR spectroscopy , 2002, AAPS PharmSciTech.

[31]  A. Sakr,et al.  Effect of anionic polymers on the release of propranolol hydrochloride from matrix tablets. , 2001, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[32]  N A Peppas,et al.  Mathematical modeling of controlled drug delivery. , 2001, Advanced drug delivery reviews.

[33]  J. Siepmann,et al.  Mathematical modeling of bioerodible, polymeric drug delivery systems. , 2001, Advanced drug delivery reviews.

[34]  A S Hussain,et al.  Identification of critical formulation and processing variables for metoprolol tartrate extended-release (ER) matrix tablets. , 1999, Journal of controlled release : official journal of the Controlled Release Society.

[35]  J. Sjögren,et al.  Investigation of prandial effects on hydrophilic matrix tablets. , 1999, Drug development and industrial pharmacy.

[36]  M. Vandelli,et al.  Drug release from perforated matrices containing hydroxypropylcellulose , 1998 .

[37]  Ali R. Rajabi-Siahboomi,et al.  A study on the interaction of water and cellulose ethers using differential scanning calorimetry , 1997 .

[38]  J. Polli,et al.  Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets. , 1997, Journal of pharmaceutical sciences.

[39]  J. Dressman,et al.  Physiochemical and physiological mechanisms for the effects of food on drug absorption: the role of lipids and pH. , 1997, Journal of pharmaceutical sciences.

[40]  P. Moldenaers,et al.  Rheological characterization of xanthan gum and hydroxypropylmethyl cellulose with respect to controlled-release drug delivery. , 1996, Journal of pharmaceutical sciences.

[41]  B. Lippold,et al.  Drug Release From Hydrocolloid Embeddings with High or Low Susceptibility to Hydrodynamic Stress , 1995, Pharmaceutical Research.

[42]  Carla Caramella,et al.  Influence of medium on dissolution-erosion behaviour of Na carboxymethylcellulose and on viscoelastic properties of gels , 1995 .

[43]  Sumio Watanabe,et al.  Water behavior during drug release from a matrix as observed using differential scanning calorimetry , 1995 .

[44]  B. Abrahamsson,et al.  Evaluation of Solubilizers in the Drug Release Testing of Hydrophilic Matrix Extended-Release Tablets of Felodipine , 1994, Pharmaceutical Research.

[45]  N. L. Stemm,et al.  Qualitative evaluation of the mechanism of release of matrix sustained release dosage forms by measurement of polymer release , 1993 .

[46]  M. Williams,et al.  Influence of ionic strength on matrix integrity and drug release from hydroxypropyl cellulose compacts , 1993 .

[47]  S. Yoshioka,et al.  Effect of Water Mobility on Drug Hydrolysis Rates in Gelatin Gels , 1992, Pharmaceutical Research.

[48]  John E. Hogan,et al.  The influence of additives on the cloud point, disintegration and dissolution of hydroxypropylmethylcellulose gels and matrix tablets , 1990 .

[49]  J. Staniforth,et al.  Powder mixing by triboelectrification , 1981 .

[50]  K. A. Khan.  The concept of dissolution efficiency , 1975, The Journal of pharmacy and pharmacology.

[51]  J D Andrade,et al.  Water and hydrogels. , 1973, Journal of biomedical materials research.

[52]  V. Thakur,et al.  Handbook of Polymers for Pharmaceutical Technologies , 2015 .

[53]  K. Dalhoff,et al.  Food-Drug Interactions , 2012, Drugs.

[54]  J. Karp,et al.  Reusable , reversibly sealable parylene membranes for cell and protein patterning , 2008 .

[55]  J. W. Moore,et al.  Mathematical comparison of dissolution profiles , 1996 .

[56]  Martyn C. Davies,et al.  Structure and behaviour in hydrophilic matrix sustained release dosage forms: 3. The influence of pH on the sustained-release performance and internal gel structure of sodium alginate matrices , 1995 .

[57]  S. Bolton,et al.  The influence of tablet density on the human oral absorption of sustained release acetaminophen matrix tablets , 1991 .

[58]  C. G. Cameron,et al.  Controlled-Release Theophylline Tablet Formulations Containing Acrylic Resins, II. Combination Resin Formulations , 1987 .

[59]  W. M. Heller,et al.  The United States Pharmacopeial Convention, Inc , 1977 .