References
- Craig DQM. Lipid matrices for sustained release: an academic overview. B T Gattefossé 2004;97:9–19
- Saraiya D, Bolton S. The use of precirol to prepare sustained-release tablets of theophylline and quinidine gluconate. Drug Dev Ind Pharm 1990;16:1963–1969
- Kumar K, Shah MH, Kethar AR, et al. Effect of drug solubility and different excipients on floating behaviour and release from glyceryl monooleate matrices. Int J Pharm 2004;272:151–160
- Barker SA, Yap SP, Yuen KH, et al. An investigation into the structure and bioavailability of alpha-tocopherol dispersions in Gelucire 44/14. J Control Release 2003;91:477–488
- Sheu MT, Hsia AHO. Polyglycolized saturated glycerides as carrier and enhancer for drug penetration. Chinese Pharm J 2001;53:107–111
- Prapaitrakul W, Sprockel OL, Shivanand P. Release of chlorphenamine maleate from fatty acid ester matrix disks prepared by melt-extrusion. J Pharm Pharmacol 1991;43:377–381
- Savolainem M, Herder J, Khoo C, et al. Evaluation of polar lipid-hydrophilic polymer microparticles. Int J Pharm 2003;262:47–62
- Khan N, Craig DQM. The influence of drug incorporation on the structure and release properties of solid dispersions in lipid matrices. J Control Release 2003;93:355–368
- Sinchaipanid N, Junyaprasert V, Mitrevej A. Application of hot melt coating for controlled release of propranolol hydrochloride pellets. Powder Technol 2004;14:203–209
- Hamdani J, Moes AJ, Amighi K. Development and evaluation of prolonged release pellets obtained by the melt pelletization process. Int J Pharm 2002;245:167–177
- Suzuki H, Onishi H, Hisamatsu S, et al. Acetaminophen-containing chewable tablets with suppressed bitterness and improved oral feeling. Int J Pharm 2004;278:51–61
- Qi S, Deutsch D, Craig DQM. An investigation into the mechanism of drug release from taste-masking fatty acid micro-spheres. J Pharm Sci 2008;97:3842–3854
- Pouton CW. Self-emulsifying drug delivery systems: assessment of the efficiency of emulsification. Int J Pharm 1985;27:335–348
- Prabhu S, Ortega M, Ma C. Novel lipid based formulations enhancing the in vitro dissolution and permeability characteristics of a poorly water-soluble model drug, piroxicam. Int J Pharm 2005;301:209–216
- Chauhan B, Shimpi S, Paradkar A. Preparation and characterization of etoricoxib solid dispersions using lipid carriers by spray drying technique. AAPS PharmSciTech 2005;6:E405--E412
- Chauhan B, Shimpi S, Mahadik KR, Paradkar A. Preparation and evaluation of floating risedronate sodium-Gelucire (R) 43/01 formulations. Drug Dev Ind Pharm 2005;31:851–860
- Li S, Lin S, Chien YW, et al. Statistical optimization of gastric floating system for oral controlled delivery of calcium. AAPS PharmSciTech 2001;1:E1
- Repka MA, Battu SK, Upadhye SB, et al. Pharmaceutical applications of hot-melt extrusion: part II. Drug Dev Ind Pharm 2007;33:1043–1057
- Thommes M, Baert L, Rosier J. 800 mg Darunavir tablets prepared by hot melt extrusion. Pharm Dev Technol 2011;16:645–650
- Tan L, Carella AJ, Ren Y, Lo JB. Process optimization for continuous extrusion wet granulation. Pharm Dev Technol 2011;16:302–315
- Breitkreutz J, El Saleh F, Kiera C, et al. Pediatric drug formulations of sodium benzoate II. Coated granules with a lipophilic binder. Eur J Pharm Biopharm 2003;56:255–260
- Reitz C, Kleinebudde P. Solid lipid extrusion of sustained release dosage forms. Eur J Pharm Biopharm 2007;67:440–448
- Michalk A, Kanikanti VR, Hamann HJ, Kleinebudde P. Controlled release of active as a consequence of the die diameter in solid lipid extrusion. J Control Release 2008;132:35–41
- Windbergs M, Strachan CJ, Kleinebudde P. Understanding the solid-state behaviour of triglyceride solid lipid extrudates and its influence on dissolution. Eur J Pharm Biopharm 2009;71:80–87
- Vithani K, Maniruzzaman M, Mostafa S, et al. Compritol® 888 ATO lipid matrices for sustained release processed by Hot-Melt Extrusion. The 39th Annual Meeting & Exposition of the Controlled Release Society; 15--18 July, 2012; Canada
- Kincl M, Meleh M, Veber M, Vrečerd F. Study of physicochemical parameters affecting the release of diclofenac sodium from lipophilic matrix tablets. Acta Chimica Slovenica 2004;51:409−425
- Sweeney G. Thermal processing of synthetic waxes for modified release solid dosage forms [thesis]. Belfast: Queen’s Belfast University; 2012
- Costa P, Lobo JMS. Modelling and comparison of dissolution profiles. Eur J Pharm Sci 2000;13:123–133
- Kitazawa S, Johno I, Mihouchi T, Okada J. Interpretation of dissolution rate data from in vitro testing of compressed tablets. J Pharm Pharmacol 1977;29:453–459
- Korsmeyer RW, Gurny R, Doelker E, et al. Mechanism of solute release from porous hydrophilic polymers. Int J Pharm 1983;15:25–35
- Siepmann J, Peppas NA. Modelling of drug release from delivery systems based on hydroxypropyl methylcellulose (HPMC). Adv Drug Deliv Rev 2001;48:139–157
- Varelas CG, Dixon DG, Steiner C. Zero order release from biphasic polymer hydrogels. J Control Release 1995;34:185–192
- 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
- Yuksel N, Kanik AE, Baykara T. Comparison of in vitro dissolution profiles by ANOVA-based, model-dependent and independent methods. Int J Pharm 2000;209:56–67