Influence of Cellulose Ether Mixtures on Ibuprofen Release: MC25, HPC and HPMC K100M

REFERENCES

• K. ParfittMartindale: The Complete Drug Reference 32th, . The Pharmaceutical Press, LondonUK 1999; 48–49
   Google Scholar
• Leo E., Forni F., Bernabei M.T. Surface drug removal ibuprofen-loaded PLA miscrospheres. Int. J. Pharm 2000; 196: 1–9, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Ilango R., Kavimani S., Jaykar B. Dissolution studies on tablets of ibuprofen using chitosan. Indian J. Experim. Biol 1999; 37: 505–508, [CSA]
   PubMedGoogle Scholar
• Salsa T., Veiga F., Pina M.E. Oral controlled-release dosage forms. I. Cellulose ether polymers in hydrophilic matrices. Drug Dev. Ind. Pharm 1997; 23(9)929–938, [CSA]
   Web of Science ®Google Scholar
• Veiga F., Salsa T., Pina M.E. Influence of technological variables on the release of theophylline from hydrophilic matrix tablets. Drug Dev. Ind. Pharm 1997; 23: 547–551, [CSA]
   Web of Science ®Google Scholar
• Pina M.E., Veiga F. The influence of diluent on the release of theophylline from hydrophilic matrix tablets. Drug Dev. Ind. Pharm 2000; 26: 1125–1128, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Khanvilkar K.H., Huang Y., Moore A.D. Influence of hydroxypropylmethylcellulose mixture, apparent viscosity, and tablet hardness on drug release using a 23 full factorial design. Drug Dev. Ind. Pharm 2000; 28(5)601–608, [CSA], [CROSSREF]
   Google Scholar
• Vázquez M.J., Perez-Marcos B., Gomes-Amoza J.L., Martinez-Pacheco R., Souto C., Concheiro A. Influence of technological variables on release of drugs from hydrophilic matrices. Drug Dev. Ind. Pharm 1992; 18(11&12)1355–1375, [CSA]
   Web of Science ®Google Scholar
• Halsas M., Simelius R., Kiviniemi A., Veski P., Jurjenson H., Marvola M. Effect of different combinations of hydropropylmethylcelluose on bioavailability of ibuprofen from press-coated time-controlled tablets. STP Pharma Sci 1998; 8(3)155–161, [CSA]
   Google Scholar
• Nokhodchi A., Rubinstein M.H. The effect of moisture on the compaction properties of the binary mixture of hydropropylmethylcelluose K4M/ibuprofen. STP Pharma Sci 1998; 8(6)349–356, [CSA]
   Google Scholar
• Nokhodchi A., Khaseh P., Ghafourian T., Siahi-Shabad M.H. The Role of various surfactants and fillers in controlling the release rate of theophylline from HPMC matrices. STP Pharma Sci 1999; 9(6)555–560, [CSA]
   Google Scholar
• Eyjofsson R. Hydropropylmethylcelluose mixtures: effects and kinetics of release of an insoluble drug. Drug Dev. Ind. Pharm 1999; 25(5)667–669, [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Dabbagh M.A., Ford J.L., Rubinstein M.H., Hogan J.E., Rajabi-Siahboomi A.R. Release of propranolol hydrochloride from matrix tablets containing sodium carboxymethylcellulose and hydroxypropylmethylcellulose. Pharm. Dev. Tech 1999; 4(3)313–324, [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Vueba M.L., Batista de Carvalho L.A.E., Veiga F., Sousa J.J., Pina M.E. Influence of cellulose ether polymers on ketoprofen release from hydrophilic matrix tablets. Eur. J. Pharm. Biopharm 2004; 58(1)51–59, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Vueba M.L., Batista de Carvalho L.A.E., Veiga F., Sousa J.J., Pina M.E. Role of cellulose ether polymers on ibuprofen release from matrix tablets. Drug Dev. Ind. Pharm 2005; 31: 653–665, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Baveja S.K., Ranga Rao K.V., Padmalatha Devi K. Zero-order release hydrophilic matrix tablets of β-adrenergic blockers. Int. J. Pharm 1987; 39: 39–45, [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Vázquez M.J., Gomes-Amoza J.L., Martinez-Pacheco R., Souto C., Concheiro A. Relationships between drug dissolution profile and gelling agent viscosity in tablets prepared with hydropropylmethylcelluose (HPMC) and sodium carboxymethylcellulose (NaCMC) mixtures. Drug Dev. Ind. Pharm 1995; 21(16)1859–1874, [CSA]
   Web of Science ®Google Scholar
• Bettini R., Colombo P., Massimo G., Catellani P.L., Vitali T. Swelling and drug release in hydrogel matrices: polymer viscosity and matrix porosity effects. Eur. J. Pharm. Sci 1994; 2: 213–219, [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Rodriguez C.F., Bruneau N., Barra J., Alfonso D., Doeker E. D.L. WiseHydrophilic cellulose derivatives as drug delivery carriers: Influence of substitution type on the properties of compressed matrix tablets. Handbook of Pharmaceutical Controlled Release Technology, . Marcel Dekker, Inc, New York/Basel 2000; 1–30
   Google Scholar
• Shah A., Jung D. Improved high-performance liquid chromatographic assay of ibuprofen in plasma. J. Chromatogra 1985; 344: 408–411, [CSA]
   PubMedGoogle Scholar
• Fell J.T., Newton J.M. Determination of tablet strength by diametral-compression test. J. Pharm. Sci 1970; 59: 688–691, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Schreiner T., Schaefer U.F., Loth H. Immediate drug release from solid oral dosage forms. J. Pharm. Sci 2005; 94(1)120–133, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Efentakis M., Vlachou M., Choulis N.H. Effects of excipients on swelling and drug release from compressed matrices. Drug Dev. Ind. Pharm 1997; 23(1)107–112, [CSA]
   Web of Science ®Google Scholar
• 24. United States Pharmacopeia 26/The National Formulary 21. U.S.P Convention, Rockville, MD, 2003
   Google Scholar
• Khan K.A., Rhodes C.T. Effect of compaction pressure on the dissolution efficiency of some direct compression systems. Pharm. Acta Helv 1972; 47: 594–607, [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Khan K.A. The concept of dissolution efficiency. J. Pharm. Pharmacol 1975; 27: 48–49, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Gibaldi M., Feldman S. Establishment of sink conditions in dissolution rate determinations-theoretical considerations and application nondisintegrating dosage forms. J. Pharm. Sci 1967; 56: 1238–1242, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Higuchi T. Rate of release of medicaments from ointment bases containing drugs in suspension. J. Pharm. Sci 1961; 50: 874–875, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Higuchi T. Mechanism of sustained-action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices. J. Pharm. Sci 1963; 52: 1145–1149, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Korsmeyer R.W., Peppas N.A. S.Z. Mansdorf, T.J. RosemanSwelling-controlled delivery systems for pharmaceutical applications: macromolecular and modelling considerations. Controlled Release Delivery Systems, . Dekker, New York 1983; 77–90
   Google Scholar
• Korsmeyer R.W., Gurny R., Doelker E.M., Buri P., Peppas N.A. Mechanism of solute release from porous hydrophilic polymers. Int. J. Pharm 1983; 15: 25–35, [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Peppas N.A. Analysis of Fickian and non-Fickian drug release from polymers. Pharm. Acta Helv 1985; 60(4)110–111, [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Ritger P.L., Peppas N.A. A simple equation for description of solute release. II Fickian and anomalous release from swellable devices. J. Control. Release 1987; 5: 37–42, [CSA], [CROSSREF]
   Google Scholar
• Higginis J.D., Gilmor T.P., Martellucci S.A., Bruce R.D., Brittain H.G. K. Floreyibuprofen. Analytical Profiles of Drug Substances, . Academic Press, New York 2001; 27: 265–299
   Google Scholar
• Wade A., Weller P.J. Handbook of Excipients 2nd. The American Pharmaceutical Association (USA) and the Pharmaceutical Press, LondonEngland 1994; 306: 223–229
   Google Scholar
• Reynolds T.D., Mitchell S.A., Balwinski K.M. Investigation of the effect of tablet surface area/volume on drug release from hydroxypropylmethylcellulose controlled-release matrix tablets. Drug Dev. Ind. Pharm 2002; 28(4)457–466, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Davidson G.W.R., Peppas N.A. Solute and penetrant diffusion in swellable polymers V. Relaxation-controlled transport in p (HEMA-co-MMA) copolymers. J. Control. Release 1986; 3: 243–258, [CSA], [CROSSREF]
   Google Scholar
• Wan L.S.C., Heng P.W.S., Wong L.F. The effect of hydroxypropylmethylcellulose on water penetration into matrix system. Int. J. Pharm 1991; 73: 111–116, [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Siepmann J., Podual K., Sriwongjanya M., Peppas N.A., Bodmeier R. A new model describing the swelling and drug release kinetics from hydroxypropylmethylcellulose tablets. J. Pharm. Sci 1999; 88(1)65–72, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Kumar V., Banker G.S. Chemically modified cellulosic polymers. Drug Dev. Ind. Pharm 1993; 19: 1–31, [CSA]
   Web of Science ®Google Scholar
• Ford J.L., Rubinstein M.H., Hogan J.E. Formulation of sustained release promethazine hydrochloride tablets using hydropropylmethlycellulose matrices. Int. J. Pharm 1985; 24: 327–338, [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• Huber H.E., Christenson G.L. Utilization of hydrophilic gums for the control of drug substance release from tablet formulations II. Influence of tablet hardness and density on dissolution behavior. J. Pharm. Sci 1968; 57(1)164–166, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar