A time-released osmotic pump fabricated by compression-coated method: Formulation screen, mechanism research and pharmacokinetic study

Satoru, 2003, Optimization of the dosage schedule for sustaining intrinsic biological rhythms, Yakugaku Zasshi, 123, 789, 10.1248/yakushi.123.789 Ohdo, 2001, Changing the dosing schedule minimizes the disruptive effects of interferon on clock function, Nat Med, 7, 356, 10.1038/85507 Litinski, 2009, Influence of the circadian system on disease Severity, Sleep Med Clin, 4, 143, 10.1016/j.jsmc.2009.02.005 Mandal, 2010, Drug delivery system based on chronobiology—A review, J Control Release, 147, 314, 10.1016/j.jconrel.2010.07.122 Liu, 2006, Preparation of monolithic osmotic pump system by coating the indented core tablet, Eur J Pharm Biopharm, 64, 180, 10.1016/j.ejpb.2006.05.004 Herrlich, 2012, Osmotic micropumps for drug delivery, Adv Drug Deliv Rev, 64, 1617, 10.1016/j.addr.2012.02.003 Lu, 2003, A water-insoluble drug monolithic osmotic tablet system utilizing gum Arabic as an osmotic, suspending and expanding agent, J Control Release, 92, 375, 10.1016/S0168-3659(03)00371-7 Theeuwes, 1975, Elementary osmotic pump, J Pharm Sci, 64, 1987, 10.1002/jps.2600641218 Liu, 2008, Solubility-modulated monolithic osmotic pump tablet for atenolol delivery, Eur J Pharm Biopharm, 68, 298, 10.1016/j.ejpb.2007.04.020 Makhija, 2003, Controlled porosity osmotic pump-based controlled release systems of pseudoephedrine I. Cellulose acetate as a semipermeable membrane, J Control Release, 89, 5, 10.1016/S0168-3659(02)00482-0 Chaudhary, 2011, Microporous bilayer osmotic tablet for colon-specific delivery, Eur J Pharm Biopharm, 78, 134, 10.1016/j.ejpb.2011.01.004 Lin, 2012, Current status and approaches to developing press-coated chronodelivery drug systems, J Control Release, 157, 331, 10.1016/j.jconrel.2011.09.065 Anoop, 2009, Analysis of factors influencing dry sliding wear behaviour of Al/SiCp–brake pad tribosystem, Mater Des, 30, 3831, 10.1016/j.matdes.2009.03.034 Hao, 2012, Development and optimization of baicalin-loaded solid lipid nanoparticles prepared by coacervation method using central composite design, Eur J Pharm Sci, 47, 497, 10.1016/j.ejps.2012.07.006 Suresha, 2010, Wear characteristics of hybrid aluminium matrix composites reinforced with graphite and silicon carbide particulates, Compos Sci Technol, 70, 1652, 10.1016/j.compscitech.2010.06.013 Levis, 2003, Use of coated microtubular halloysite for the sustained release of diltiazem hydrochloride and propranolol hydrochloride, Int J Pharm, 253, 145, 10.1016/S0378-5173(02)00702-0 Diler, 2013, Main and interaction effects of matrix particle size, reinforcement particle size and volume fraction on wear characteristics of Al–SiCp composites using central composite design, Compos Part B-Eng, 50, 371, 10.1016/j.compositesb.2013.02.001 Varshosaz, 2010, Development and optimization of solid lipid nanoparticles of amikacin by central composite design, J Liposome Res, 20, 97, 10.3109/08982100903103904 Zhang, 2013, Optimization of Jiawei Qing'e oral fast disintegrating tablets based on response surface-central composite design, Chin Herb Med, 5, 138 Lin, 2001, Compression forces and amount of outer coating layer affecting the time-controlled disintegration of the compression-coated tablets prepared by direct compression with micronized ethylcellulose, J Pharm Sci, 90, 2005, 10.1002/jps.1151 Marucci, 2010, Osmotic pumping release from ethyl–hydroxypropyl–cellulose-coated pellets: a new mechanistic model, J Control Release, 142, 53, 10.1016/j.jconrel.2009.10.009 Pabari, 2012, Application of face centred central composite design to optimise compression force and tablet diameter for the formulation of mechanically strong and fast disintegrating orodispersible tablets, Int J Pharm, 430, 18, 10.1016/j.ijpharm.2012.03.021 Zhang, 2007, Central composite experimental design applied to the catalytic aromatization of isophorone to 3,5-xylenol, Chemom Intell Lab Syst, 89, 45, 10.1016/j.chemolab.2007.05.006 Fan, 2001, An investigation of pulsatile release tablets with ethylcellulose and Eudragit L as film coating materials and cross-linked polyvinylpyrrolidone in the core tablets, J Control Release, 77, 245, 10.1016/S0168-3659(01)00508-9 Savastano, 1995, Membrane modulated dissolution of oral drug delivery systems, Pharm Acta Helv, 70, 117, 10.1016/0031-6865(94)00056-2 Adnan, 1980, Dissolution of hard gelatin capsules I. Simple method for calculating the rate constant, Int J Pharm, 5, 79, 10.1016/0378-5173(80)90052-6