Role of Cellulose Ether Polymers on Ibuprofen Release from Matrix Tablets

References

• Alderman, D. A. (1984). A review of cellulose ethers in hydrophilic matrices for oral controlled-release dosage forms. International Journal of Pharmaceutical Technology & Product Manufacture, 5(3), 1–9.
   Google Scholar
• Alvarez-Lorenzo, C., Gómez-Amoza, J. L., Martínez-Pacheco, R., Souto, C., & Concheiro, A. (2000). The stability of theophylline tablets with a hydroxypropylcellulose matrix. Drug Development and Industrial Pharmacy, 26, 13–20., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Amado, A. M., & Ribeiro-Claro, P. J. A. (2000). Selection of substituted benzaldehyde conformers by the cyclodextrin inclusion process: a Raman spectroscopic study. Journal of Raman Spectroscopy, 31, 971–978., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Baumgartner, S., Smid-Korbar, J., Vrecer, F., & Kristl, J. (1998). Physical and technological parameters influencing floating properties of matrix tablets based on cellulose ethers. STP Pharma Sciences, 8, 285–290., [CSA]
   Google Scholar
• Bettini, R., Colombo, P., Massimo, G., Catellani, P. L., & Vitali, T. (1994). Swelling and drug release in hydrogel matrices: polymer viscosity and matrix porosity effects. European Journal of Pharmaceutical Sciences, 2, 213–219., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Bi, Y. X., Sunada, H., Yonezawa, Y., & Danjo, K. (1999). Evaluation of rapidly disintegrating tablets prepared by a direct compression method. Drug Development and Industrial Pharmacy, 25(5), 571–581., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Bibby, D. C., Davies, N. M., & Tucker, I. G. (2000). Mechanisms by which cyclodextrins modify drug release from polymeric drug delivery systems. International Journal of Pharmaceutics, 197, 1–11., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Braga, S. S., Gonçalves, I. S., Herdtweck, E., & Teixeira-Dias, J. J. C. (2003). Solid state inclusion compound of S-ibuprofen in β-cyclodextrin: structure and characterisation. New Journal of Chemistry, 3, 597–601., [CSA], [CROSSREF]
   Google Scholar
• Cheong, L. W. S., Heng, P. W. S., & Wong, L. P. (1992). Relationship between polymer viscosity and drug release release from a matrix system. Pharmaceutical Research, 9(11), 1510–1514., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Ebube, N. K., & Jones, A. B. (2004). Sustained release of acetaminophen from a heterogeneous mixture of two hydrophilic non-ionic cellulose ether polymers. International Journal of Pharmaceutics, 272, 19–27., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Efentakis, M., Vlachou, M., & Choulis, N. H. (1997). Effects of excipients on swelling and drug release from compressed matrices. Drug Development and Industrial Pharmacy, 23(1), 107–112., [CSA]
   Web of Science ®Google Scholar
• Fell, J. T., & Newton, J. M. (1970). Determination of tablet strength by diametral-compression test. Journal of Pharmaceutical Sciences, 59, 688–691., [PUBMED], [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Ford, J. L. (1999). Thermal analysis of hydroxypropylmethylcellulose and methylcellulose: powders, gels and matrix tablets. International Journal of Pharmaceutics, 179, 209–228., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Ghosh, L. K., Ghosh, N. C., Chatterjee, M., & Gupta, B. K. (1998). Product development studies on the tablet formulation of ibuprofen to improve bioavailability. Drug Development and Industrial Pharmacy, 24(5), 473–477., [PUBMED], [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Higginis, J. D., Gilmor, T. P., Martellucci, S. A., Bruce, R. D., & Brittain, H. G. (2001). Ibuprofen. In: Florey, K. (Ed.). Analytical Profiles of Drug Substances, Vol. 27. New York: Academic Press, 265–299.
   Google Scholar
• Higuchi, T. (1961). Rate of release of medicaments from ointment bases containing drugs in suspension. Journal of Pharmaceutical Sciences, 50, 874–875., [PUBMED], [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Higuchi, T. (1963). Mechanism of sustained-action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices. Journal of Pharmaceutical Sciences, 52, 1145–1149., [PUBMED], [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Khan, K. A. (1975). The concept of dissolution efficiency. Journal of Pharmacy and Pharmacology, 27, 48–49., [PUBMED], [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Khan, K. A., & Rhodes, C. T. (1972). Effect of compaction pressure on the dissolution efficiency of some direct compression systems. Pharmaceutica Acta Helvetiae, 47, 594–607., [PUBMED], [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Korsmeyer, R. W., Gurny, R., Doelker, E. M., Buri, P., & Peppas, N. A. (1983). Mechanism of solute release from porous hydrophilic polymers. International Journal of Pharmaceutics, 15, 25–35., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Kumar, V., & Banker, G. S. (1993). Chemically modified cellulosic polymers. Drug Development and Industrial Pharmacy, 19, 1–31., [CSA]
   Web of Science ®Google Scholar
• Lu, D. R., Abu-Izza, K., & Chen, W. (1996). Optima: a windows-based program for computer-aided optimisation of controlled-release dosage forms. Pharmaceutical Development and Technology, 1(4), 405–414., [PUBMED], [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Martindale, W. (1999). The Complete Drug Reference (32nd ed.). London: The Pharmaceutical Press, 48–49.
   Google Scholar
• Mcphillips, H., Craig, D. Q. M., Royal, P. G., & Hill, V. L. (1999). Characterisation of the glass transition of HPMC using modulated temperature differential scanning calorimetry. International Journal of Pharmaceutics, 180, 83–90., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Mitchell, K., Ford, J. L., Armstrong, D. J., Elliott, P. N. C., Rostron, C., & Hogan, J. E. (1993a). The influence of concentration on the release of drugs from gels and matrices containing Methocel®. International Journal of Pharmaceutics, 100, 155–163., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Mitchell, K., Ford, J. L., Armstrong, D. J., Elliott, P. N. C., Rostron, C., & Hogan, J. E. (1993b). The influence of concentration on the properties of gels and swelling characteristics of matrices containing methylcellulose or hydroxypropylmethylcellulose. International Journal of Pharmaceutics, 100, 165–173., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Monti, S., Sortino, S., De Guidi, G., & Marconi, G. (1998). Supramolecular photochemistry of 2-(3-benzoylphenyl) propionic acid (ketoprofen). A study in the β-cyclodextrin cavity. New Journal of Chemistry, 599–604., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Mura, P., Manderioli, A., Bramati, G., Furlanetto, S., & Pinzauti, S. (1995). Utilization of differential scanning calorimetry as a screening technique to determine the compatibility of ketoprofen with excipients. International Journal of Pharmaceutics, 119, 71–79., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Mura, P., Bettinetti, G. P., Manderioli, A., Faucci, M. T., Bramanti, G., & Sorrenti, M. (1998). Interactions of ketoprofen and ibuprofen in solution and in solid state. International Journal of Pharmaceutics, 166, 189–203., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Nokhodchi, A., Ford, J. L., Rowe, P. H., & Rubinstein, M. H. (1996). The effects of compression rate and force on the compaction properties of different viscosity grades of hydroxypropylmethylcellulose 2208. International Journal of Pharmaceutics, 129, 21–31., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Panomsuk, S. P., Hatanaka, T., Aiba, T., Katayama, K., & Koizumi, T. (1995). A study of the hydrophilic cellulose matrix: effect of indomethacin and a water-soluble additive on release mechanisms. Chemical and Pharmaceutical Bulletin, 43(6), 994–999., [CSA]
   Web of Science ®Google Scholar
• Peppas, N. A. (1985). Analysis of Fickian and non-Fickian drug release from polymers. Pharmaceutica Acta Helvetiae, 60(4), 110–111., [PUBMED], [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Pifferi, G., & Restani, P. (2003). The safety of pharmaceutical excipients. Il Farmaco, 58, 541–550., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Pina, M. E., & Veiga, F. (2000). The influence of diluent on the release of theophylline from hydrophilic matrix tablets. Drug Development and Industrial Pharmacy, 26, 1125–1128., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Rajabi-Siahboomi, A. R. (1998). Slow release hydrophilic matrix systems: investigation of the interactions between water and hydroxypropylmethylcellulose. In: Proceedings of the 25th International Symposium on Controlled Release of Bioactive Materials. Controlled Release Society, Inc., 52–53.
   Google Scholar
• Ranga Rao, K. V., Padmalatha, D., & Buri, P. (1988). Cellulose matrices for zero-order release of soluble drugs. Drug Development and Industrial Pharmacy, 14, 2299–2320., [CSA]
   Web of Science ®Google Scholar
• Ritger, P. L., & Peppas, N. A. (1987). A simple equation for description of solute release. II Fickian and anomalous release from swellable devices. Journal of Controlled Release, 5, 37–42., [CSA], [CROSSREF]
   Google Scholar
• Rodriguez, C. F., Bruneau, N., Barra, J., Alfonso, D., & Doelker, E. (2000). Hydrophilic cellulose derivatives as drug delivery carriers: influence of substitution type on the properties of compressed matrix tablets. In: Wise, D. L. (Ed.). Handbook of Pharmaceutical Controlled Release Technology. New York: Marcel Dekker, Inc., 1–30.
   Google Scholar
• Roy, D. S., & Rodera, B. D. (2002). Comparative evaluation of rate of hydration and matrix erosion of HEC and HPC and study of drug release from their matrices. European Journal of Pharmaceutical Sciences, 16, 193–199., [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Salsa, T., Veiga, F., Teixeira-Dias, J. J. C., & Pina, M. E. (2003). Effect of polymer hydration on the kinetic release of drugs: a study of ibuprofen and ketoprofen in HPMC matrices. Drug Development and Industrial Pharmacy, 29(3), 289–297., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Schreiner, T., Schaefer, U. F., & Loth, H. (2005). Immediate drug release from solid oral dosage forms. Journal of Pharmaceutical Sciences, 94(1), 120–133., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Siepmann, J., Kranz, H., & Bodmeier, R. (1999). HPMC-matrices for controlled drug delivery: a new model combining diffusion, swelling, and dissolution mechanisms and predicting the release kinetics. Pharmaceutical Research, 16, 1748–1756., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Steiner, T., & Koellner, G. (1994). Crystalline β-cyclodextrin hydrate at various humidities: fast, continuous and reversible dehydration studied by X-ray diffraction. Journal of the American Chemical Society, 116, 5122–5128., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Steiner, T., Moreira Da Silva, A. M., Teixeira-Dias, J. J. C., Mueller, J., & Saenger, W. (1995). Rapid water diffusion in a cage-type crystal lattice: β-cyclodextrin dodecahydrate. Angewandte Chemie. International Edition in English, 34, 1452–1453., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Sung, K. C., Nixon, P. R., Skoug, J. W., Ju, T. R., Gao, P., Topp, E. M., & Patel, M. V. (1996). Effect of formulation variables on drug and polymer release from HPMC-base matrix tablets. International Journal of Pharmaceutics, 142, 53–60., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• The United States Pharmacopeia 25/The National Formulary 20 (2002). In U.S.P. Convention, Rockville.
   Google Scholar
• Vazquez, M. J., Perez-Marcos, B., Gomes-Amoza, J. L., Martinez-Pacheco, R., Souto, C., & Concheiro, A. (1992). Influence of technological variables on release of drugs from hydrophilic matrices. Drug Development and Industrial Pharmacy, 18, 1355–1375., [CSA]
   Web of Science ®Google Scholar
• Veiga, F., Salsa, T., & Pina, M. E. (1997). Influence of technological variables on the release of theophylline from hydrophilic matrix tablets. Drug Development and Industrial Pharmacy, 23, 547–551., [CSA]
   Web of Science ®Google Scholar
• Velasco, M. V., Ford, J. L., Rowe, P., & Rajabi-Siahboomi, A. R. (1999). Influence of drug: hydroxypropylmethylcellulose ratio, drug and polymer particle size and compression force on the release of diclofenac sodium from HPMC tablets. Journal of Controlled Release, 57, 75–85., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Vergnaud, J. M. (1993). Liquid transport controlled release processes in polymeric materials: applications to oral dosage forms. International Journal of Pharmaceutics, 90, 89–94., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Vueba, M. L., Batista De Carvalho, L. A. E., Veiga, F., Sousa, J. J., & Pina, M. E. (2004). Influence of cellulose ether polymers on ketoprofen release from hydrophilic matrix tablets. European Journal of Pharmaceutics and Biopharmaceutics, 58(1), 51–59., [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Wade, A., & Weller, P. J. (1994). Handbook of Pharmaceutical Excipients (2nd ed.). London: The Pharmaceutical Press, , pp. 223–229, 306.
   Google Scholar
• Wan, L. S. C., Heng, P. W. S., & Wong, L. F. (1991). The effect of hydroxypropylmethylcellulose on water penetration into matrix system. International Journal of Pharmaceutics, 73, 111–116., [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Wan, L. S. C., Heng, P. W. S., & Wong, L. F. (1993). Relationship between swelling and drug release in a hydrophilic matrix. Drug Development and Industrial Pharmacy, 19(10), 1201–1210., [CSA]
   Web of Science ®Google Scholar
• Wan, L. S. C., Heng, P. W. S., & Wong, L. F. (1995). Matrix swelling: a simple model describing extent of swelling of HPMC matrices. International Journal of Pharmaceutics, 116, 159–168., [CSA], [CROSSREF]
   Web of Science ®Google Scholar