References
- Varma MV, Kaushal AM, Garg A, and Garg S. Factors affecting mechanism and kinetics of drug release from matrix based oral controlled drug delivery systems. Am J Drug Deliv 2004;1:43–57.
- Jantzen GM, Robinson JR. Sustaind and controlled release drug delivery systems. In: Banker GS, Rhodes C (eds.), Modern Pharmaceutics, 3rd edn. Marcel Dekker, New York, 1996, pp. 575–610.
- Qui YZ, Zhang G. Research and development aspects of oral controlled release dosage forms. In: Wise DL (ed.), Handbook of Pharmaceutical Controlled Release Technology. Marcel Dekker, New York, 2000, pp. 465–503.
- Hui HW, Robinson JR, Lee VH. Design and fabrication of oral controlled release drug delivery systems. In: Robinson JR, Lee VH (eds.), Cotrolled Drug Delivery, Fundemental and Application, 2nd edn. Marcel Dekker, New York, 1987, pp. 373–432.
- Tahara K, Yamamoto M, Nishihata T. Overall mechanism behind matrix sustained release (SR) tablets prepared with hydroxypropyl methylcellulose. J Control Release 1995;35:59–66.
- Toution E, Donbrow M. Influence of additives on hydroxy ethyl methyl cellulose properties: relation between gelation temperature changes, compressed matrix integrity and drug release profile. Int J Pharm 1982;11:131–148.
- Neau SH, Chow MY, Durrani MJ. Fabrication and characterization of extruded and spheronized beads containing Carbopol(R) 974P, NF resin. Int J Pharm 1996;131:47–55.
- Khan GM, Zhu JB. Studies on drug release kinetics from ibuprofen-carbomer hydrophilic matrix tablets: influence of co-excipients on release rate of the drug. J Control Release 1999;57:197–203.
- Pongjanyakul T, Parakongpan S, Rungsardthong U, Chancham P, Priprem A. Characteristics and in vitro release of Dextromethorphan resinates. Powder Technol 2005;152:100–106.
- Bharag SS, Taka S, Sakr A. Development and in vivo evaluation of extended release dextromethorphan tablets. Pharm Ind 2006;68:116–119.
- Bharag SS, Taka S, Sakr A. Development and in vivo evaluation of extended release dextromethorphan tablets. Pharm Ind 2006;68:247–249.
- Korsmeyer RW, Gurny R, Docler E, Buri P, Peppas NA. Mechanism of solute release from porous hydrophilic polymers. Int J Pharm 1983;15:25–35.
- FDA. ICH harmonised tripartite guideline, stability testing of new drug substances and products Q1A (R2) (2003).
- Ranga-Rao KV, Devi KP. Swelling controlled release systems: Recent developments and applications. Int J Pharm 1988;48:1–16.
- Seng CH, Hasaesum P, Peggy K, Robinson JR. Bioadhesive polymers as platforms for oral controlled release drug delivery II: Synthesis and evaluation of some swelling, water-insoluble bioadhesive polymers. J Pharm Sci 1985;74:399–405.
- Khan GM, Jiabi Z. Formulation and in vitro evaluation of ibuprofen-Carbopol 974P-NF controlled release matrix tablets. III: Influence of co-excipients on release rate of the drug. J Control Release 1998;54:185–190.
- Taka S, Bharag SS, Sakr A. Influence of methacrylic acid and hydroxypropylmethyl cellulose on the tablet properties and in vitro release of dextromethorphan hydrobromide. Pharmazie 2003;58:886–890.
- Samani SM, Montaseri H, Kazemi A. The effect of polymer blends on release profiles of diclofenac sodium from matrices. Eur J Pharm Biopharm 2003;55:351–355.
- Rao YM, Veni JK, Jayasagar G. Formulation and evaluation of diclofenac sodium using hydrophilic matrices. Drug Dev Ind Pharm 2001;27:759–766.
- Anlar S, Capan Y, Güven O, Gögüs A, Dalkara T, Hincal AA. Formulation and in vitro-in vivo evaluation of buccoadhesive morphine sulfate tablets. Pharm Res 1994;11:231–236.
- Siepmann J, Peppas NA. Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose (HPMC). Adv Drug Deliv Rev 2001;48:139–157.