Development of controlled release tablet by optimizing HPMC: consideration of theoretical release and RSM.

[1]  S. Patra,et al.  Optimization of HPMC and carbopol concentrations in non-effervescent floating tablet through factorial design. , 2014, Carbohydrate polymers.

[2]  L. Nath,et al.  Compatibility studies of nateglinide with excipients in immediate release tablets , 2011, Acta pharmaceutica.

[3]  B. Bhunia,et al.  Extracellular alkaline protease from Bacillus licheniformis NCIM‐2042: Improving enzyme activity assay and characterization , 2011 .

[4]  B. Bhunia,et al.  Formulation, development, and optimization of immediate release nateglinide tablets by factorial design. , 2010, Drug discoveries & therapeutics.

[5]  R. Fassihi,et al.  Development of a controlled release low dose class II drug-Glipizide. , 2006, International journal of pharmaceutics.

[6]  R. Fassihi,et al.  Analysis of macromolecular changes and drug release from hydrophilic matrix systems. , 2005, International journal of pharmaceutics.

[7]  R. Fassihi,et al.  Formulation Development and Human In Vitro‐In Vivo Correlation for a Novel, Monolithic Controlled‐Release Matrix System of High Load and Highly Water‐Soluble Drug Niacin , 2004, Drug development and industrial pharmacy.

[8]  J. McLeod Clinical Pharmacokinetics of Nateglinide , 2004, Clinical pharmacokinetics.

[9]  H. Nakashima,et al.  Influence of water soluble fillers in hydroxypropylmethylcellulose matrices on in vitro and in vivo drug release. , 2002, Journal of controlled release : official journal of the Controlled Release Society.

[10]  Nils-Olof Lindberg,et al.  Multivariate methods in pharmaceutical applications , 2002 .

[11]  R. Williams,et al.  Investigation of Excipient Type and Level on Drug Release from Controlled Release Tablets Containing HPMC , 2002, Pharmaceutical development and technology.

[12]  A. Sakr,et al.  Application of multiple response optimization technique to extended release formulations design. , 2001, Journal of controlled release : official journal of the Controlled Release Society.

[13]  B. Narasimhan,et al.  Mathematical models describing polymer dissolution: consequences for drug delivery. , 2001, Advanced drug delivery reviews.

[14]  N A Peppas,et al.  Translocation of drug particles in HPMC matrix gel layer: effect of drug solubility and influence on release rate. , 2001, Journal of controlled release : official journal of the Controlled Release Society.

[15]  S. Garg,et al.  Evaluation of the compatibility of ketorolac tromethamine with selected polymers and common tablet excipients by thermal and isothermal stress testing , 2001 .

[16]  N. Peppas,et al.  Observation of swelling process and diffusion front position during swelling in hydroxypropyl methyl cellulose (HPMC) matrices containing a soluble drug. , 1999, Journal of controlled release : official journal of the Controlled Release Society.

[17]  T. Lundstedt,et al.  Experimental design and optimization , 1998 .

[18]  J. Fredrickson,et al.  A mixture experiment approach for controlling the dissolution rate of a sustained-release tablet. , 1998, Drug development and industrial pharmacy.

[19]  Kozo Takayama,et al.  Multi-objective simultaneous optimization technique based on an artificial neural network in sustained release formulations , 1997 .

[20]  P. R. Nixon,et al.  Swelling of hydroxypropyl methylcellulose matrix tablets. 2. Mechanistic study of the influence of formulation variables on matrix performance and drug release. , 1996, Journal of Pharmacy and Science.

[21]  H. Kurahashi,et al.  Influence of Physicochemical Properties on Drug Release Rate from Hydroxypropylmethylcellulose Matrix Tablets. , 1996 .

[22]  R. Renoux,et al.  Experimentally Designed Optimization of Direct Compression Tablets , 1996 .

[23]  C. Rostron,et al.  The influence of concentration on the release of drugs from gels and matrices containing Methocel , 1993 .

[24]  J. Kost Controlled drug delivery systems , 1989, Proceedings. ICCON IEEE International Conference on Control and Applications.

[25]  John E. Hogan,et al.  Importance of drug type, tablet shape and added diluents on drug release kinetics from hydroxypropylmethylcellulose matrix tablets , 1987 .

[26]  N. Peppas,et al.  Mechanisms of solute release from porous hydrophilic polymers , 1983 .

[27]  Joseph L. Kanig,et al.  The theory and practice of industrial pharmacy , 1970 .

[28]  T. Higuchi MECHANISM OF SUSTAINED-ACTION MEDICATION. THEORETICAL ANALYSIS OF RATE OF RELEASE OF SOLID DRUGS DISPERSED IN SOLID MATRICES. , 1963, Journal of pharmaceutical sciences.