Comparative evaluation of drug release from aged prolonged polyethylene oxide tablet matrices: effect of excipient and drug type

References

• Ebube NK, Hikal AH, Wyandt CM, et al. Sustained release of acetaminophen from heterogeneous matrix tablets: influence of polymer ratio, polymer loading, and co-active on drug release. Pharm Dev Technol 1997;2:161–170
   PubMedGoogle Scholar
• Kaialy W, Emami P, Asare-Addo K, et al. Psyllium: a promising polymer for sustained release formulations in combination with HPMC polymers. Pharm Dev Technol 2013;19:269–277
   PubMed Web of Science ®Google Scholar
• Waterman KC, MacDonald BC, Roy MC. Extrudable core system: development of a single-layer osmotic controlled-release tablet. J Control Release 2009;134:201–206
   PubMed Web of Science ®Google Scholar
• Vogelhuber W, Magni E, Mouro M, et al. Monolithic triglyceride matrices: a controlled-release system for proteins. Pharm Dev Technol 2003;8:71–79
   PubMed Web of Science ®Google Scholar
• Williams III RO, Reynolds TD, Cabelka TD, et al. Investigation of excipient type and level on drug release from controlled release tablets containing HPMC. Pharm Dev Technol 2002;7:181–193
   PubMed Web of Science ®Google Scholar
• Huang X, Brazel CS. On the importance and mechanisms of burst release in matrix-controlled drug delivery systems. J Contr Rel 2001;73:121–136
   PubMed Web of Science ®Google Scholar
• Maggi L, Bruni R, Conte U. High molecular weight polyethylene oxides (PEOs) as an alternative to HPMC in controlled release dosage forms. Int J Pharm 2000;195:229–238
   PubMed Web of Science ®Google Scholar
• Efentakis M, Vlachou M. Evaluation of high molecular weight poly (oxyethylene)(Polyox) polymer: studies of flow properties and release rates of furosemide and captopril from controlled-release hard gelatin capsules. Pharm Dev Technol 2000;5:339–346
   PubMed Web of Science ®Google Scholar
• Alderman D. A review of cellulose ethers in hydrophilic matrices for oral controlled-release dosage forms. Int J Pharm Tech Prod Mfr 1984;5:1–9
   Web of Science ®Google Scholar
• Shah AP, Bhandary SR. POLYOX (polyethylene oxide)-applications in pharma industry. Available from: http://www.pharmainfo.net/reviews/polyox-polyethylene-oxide-applications-pharma-industry [last accessed 31 Jul 2014]
   Google Scholar
• Dimitrov M, Lambov N. Study of verapamil hydrochloride release from compressed hydrophilic polyox-wsr tablets. Int J Pharm 1999;189:105–111
   PubMed Web of Science ®Google Scholar
• Maggi L, Segale L, Torre M, et al. Dissolution behaviour of hydrophilic matrix tablets containing two different polyethylene oxides (PEOs) for the controlled release of a water-soluble drug. Dimensionality study. Biomaterials 2002;23:1113–1119
   PubMed Web of Science ®Google Scholar
• Ku MS. Preformulation consideration for drugs in oral CR formulation. In: Wen H, Park K, eds. Oral controlled release formulation design and drug delivery: theory to practice. Hoboken (NJ): John Wiley & Sons; 2010:47–70
   Google Scholar
• Bigger S, Scheirs J, Delatycki O, Billingham N. Effects of frequency, molecular weight and thermal oxidation on the dynamic mechanical response of poly (ethylene oxide). Polym Int 1991;26:181–186
   Web of Science ®Google Scholar
• Mkhatresh OA, Heatley F. A study of the products and mechanism of the thermal oxidative degradation of poly (ethylene oxide) using 1H and 13C 1-D and 2-D NMR. Polym Int 2004;53:1336–1342
   Web of Science ®Google Scholar
• Prodduturi S, Manek RV, Kolling WM, et al. Solid-state stability and characterization of hot-melt extruded poly (ethylene oxide) films. J Pharm Sci 2005;94:2232–2245
   PubMed Web of Science ®Google Scholar
• Shojaee S, Cumming I, Kaialy W, Nokhodchi A. The influence of vitamin E succinate on the stability of polyethylene oxide PEO controlled release matrix tablets. Colloid Surf B 2013;111:486–92
   PubMed Web of Science ®Google Scholar
• Crowley MM, Zhang F, Koleng JJ, McGinity JW. Stability of polyethylene oxide in matrix tablets prepared by hot-melt extrusion. Biomaterials 2002;23:4241–4248
   PubMed Web of Science ®Google Scholar
• Puz MJ, Johnson BA, Murphy BJ. Use of the antioxidant BHT in asymmetric membrane tablet coatings to stabilize the core to the acid catalyzed peroxide oxidation of a thioether drug. Pharm Dev Technol 2005;10:115–125
   PubMed Web of Science ®Google Scholar
• Florence AT, Attwood D. Physicochemical principles of pharmacy. London, UK: Pharmaceutical Press; 2011:95–98
   Google Scholar
• Michoel A, Rombaut P, Verhoye A. Comparative evaluation of co-processed lactose and microcrystalline cellulose with their physical mixtures in the formulation of folic acid tablets. Pharm Dev Technol 2002;7:79–87
   PubMed Web of Science ®Google Scholar
• Kaialy W, Martin GP, Ticehurst MD, et al. Characterisation and deposition studies of recrystallised lactose from binary mixtures of ethanol/butanol for improved drug delivery from dry powder inhalers. AAPS J 2011;13:30–43
   PubMed Web of Science ®Google Scholar
• Kaialy W, Ticehurst M, Nokhodchi A. Dry powder inhalers: mechanistic evaluation of lactose formulations containing salbutamol sulphate. Int J Pharm 2012;423:184–194
   PubMed Web of Science ®Google Scholar
• Rane M, Parmar J, Rajabi-Siahboomi A. Hydrophilic matrices for oral extended release. Pharm Times 2010;42:41–45
   Google Scholar
• Kaialy W, Larhrib H, Chikwanha B, et al. An approach to engineer paracetamol crystals by antisolvent crystallization technique in presence of various additives for direct compression. Int J Pharm 2014;464:53–64
   PubMed Web of Science ®Google Scholar
• US Pharmacopeia 26-National Formulary 21. Rockville (MD): USP Convention Inc.; 2003, 320 p
   Google Scholar
• Moore JW, Flanner HH. Mathematical comparison of dissolution profiles. Pharm Technol 1996;20:64–74
   Google Scholar
• Shojaee S, Asare-Addo K, Kaialy W, et al. An investigation into the stabilization of diltiazem HCL release from matrices made from aged polyox powders. AAPS PharmSciTech 2013;14:1190–98
   PubMed Web of Science ®Google Scholar
• Nokhodchi A, Javadzadeh Y. The effect of storage conditions on the physical stability of tablets. Pharmaceut Technol Europe 2007;19:20–26
   Google Scholar
• Wieczorek, W, Raducha D, Zalewska A, Stevens JR. Effect of salt concentration on the conductivity of PEO-based composite polymeric electrolytes. J Phys Chem B 1998;102:8725–8731
   Web of Science ®Google Scholar
• Boyapally H, Nukala RK, Bhujbal P, Douroumis D. Controlled release from directly compressible theophylline buccal tablets. Coll Surf B: Biointerf 2010;77:227–233
   PubMed Web of Science ®Google Scholar
• Hote-Gaston JL, Wallick D. Effect of filler type on the stability of polyethylene oxide in a hydrophilic matrix tablet. In: 35th Annual Meeting and Exposition of the Controlled Release Society; New York, NY; 2008
   Google Scholar
• Levina M, Rajabi-Siahboomi AR. The influence of excipients on drug release from hydroxypropyl methylcellulose matrices. J Pharm Sci 2004;93:2746–2754
   PubMed Web of Science ®Google Scholar
• Tukaram BN, Rajagopalan IV, Shartchandra PSI. The effects of lactose, microcrystalline cellulose and dicalcium phosphate on swelling and erosion of compressed HPMC matrix tablets: texture analyzer. Iran J Pharm Res 2010;9:349–358
   PubMed Web of Science ®Google Scholar
• Sako K, Sawada T, Nakashima H, et al. Influence of water soluble fillers in hydroxypropylmethylcellulose matrices on in vitro and in vivo drug release. J Control Release 2002;81:165–172
   PubMed Web of Science ®Google Scholar
• El-Malah Y, Nazzal S, Khanfar NM. D-optimal mixture design: optimization of ternary matrix blends for controlled zero-order drug release from oral dosage forms. Drug Dev Ind Pharm 2006;32:1207–1218
   PubMed Web of Science ®Google Scholar