Development of gastro intestinal sustained release tablet formulation containing acryl-EZE and pH-dependent swelling HPMC K 15 M

References

• Caraballo Isidoro. (2010). Factors affecting drug release from hydroxypropyl methylcellulose matrix systems in the light of classical and percolation theories. Expert Opin Drug Deliv 7:1291–1301.
   PubMed Web of Science ®Google Scholar
• De Castro WV, Pires MA, Oliveira MA, Vianna-Soares CD, Nunan EA, Pianetti GA et al. (2006). The influence of formulation on the dissolution profile of diclofenac sodium tablets. Drug Dev Ind Pharm, 32:1103–1109.
   PubMed Web of Science ®Google Scholar
• Dreu Rok, Ilić Ilija, Srčič Stanko. (2011). Development of a multiple-unit tablet containing enteric-coated pellets. Drug Dev Ind Pharm, 16:118–126.
   Google Scholar
• Evans DF, Pye G, Bramley R, Clark AG, Dyson TJ, Hardcastle JD. (1988). Measurement of gastrointestinal pH profiles in normal ambulant human subjects. Gut, 29:1035–1041.
   PubMed Web of Science ®Google Scholar
• Faith A. Chaibva, Sandile M.M. Khamanga, Roderick B. Walker. (2010). Swelling, erosion and drug release characteristics of salbutamol sulfate from hydroxypropyl methylcellulose-based matrix tablets. Drug Dev Ind Pharm, 36:1497–1510.
   Google Scholar
• Ford JL, Rubinstein MH, Hogan JH. (1985). Formulation of sustained release promethazine hydrochloride tablets using hydroxypropyl-methylcellulose matrices. Int J Pharm, 24:327–338.
   Web of Science ®Google Scholar
• Ford JL, Rubinstein MH, Hogan JE. (1985). Propranolol hydrochloride and aminophylline release from matrix tablets containing hydroxypropylmethylcellulose. Int J Pharm, 24:339–350.
   Web of Science ®Google Scholar
• Fu XC, Wang GP, Liang WQ, Chow MS. (2004). Prediction of drug release from HPMC matrices: effect of physicochemical properties of drug and polymer concentration. J Control Release, 95:209–216.
   PubMed Web of Science ®Google Scholar
• Gurny R, Doelker E, Peppas NA. (1982). Modelling of sustained release of water-soluble drugs from porous, hydrophobic polymers. Biomaterials, 3:27–32.
   PubMed Web of Science ®Google Scholar
• Guidance for industry. August 1997. Dissolution testing of immediate release solid oral dosage forms. US Department of Health and Human Services, CDER.
   Google Scholar
• Higuchi T. (1961). Rate of release of medicaments from ointment bases containing drugs in suspension. J Pharm Sci, 50:874–875.
   PubMed Web of Science ®Google Scholar
• Higuchi T. (1963). Mechanism of sustained-action medication. theoretical analysis of rate of release of solid drugs dispersed in solid matrices. J Pharm Sci, 52:1145–1149.
   PubMed Web of Science ®Google Scholar
• Khanna R, Agarwal SP, Ahuja A. (1997). Muco-adhesive buccal tablets of clotrimazole for oral candidiasis. Drug Dev Ind Pharm, 23:831–837.
   Web of Science ®Google Scholar
• Kiortsis S, Kachrimanis K, Broussali T, Malamataris S. (2005). Drug release from tableted wet granulations comprising cellulosic (HPMC or HPC) and hydrophobic component. Eur J Pharm Biopharm, 59:73–83.
   PubMed Web of Science ®Google Scholar
• Korsmeyer RW, Gurnya R, Doelker E, Buri P, Peppas NA. (1983). Mechanisms of solute release from porous hydrophilic polymers. Int J Pharm, 15, 25–35.
   Web of Science ®Google Scholar
• Lee BJ, Ryu SG, Cui JH. (1999). Formulation and release characteristics of hydroxypropyl methylcellulose matrix tablet containing melatonin. Drug Dev Ind Pharm, 25:493–501.
   PubMed Web of Science ®Google Scholar
• Li CL, Martini LG, Ford JL, Roberts M. (2005). The use of hypromellose in oral drug delivery. J Pharm Pharmacol, 57:533–546.
   PubMed Web of Science ®Google Scholar
• Li S, Lin S, Daggy BP, Mirchandani HL, Chien YW. (2003). Effect of HPMC and Carbopol on the release and floating properties of Gastric Floating Drug Delivery System using factorial design. Int J Pharm, 253:13–22.
   PubMed Web of Science ®Google Scholar
• Madhusudan Rao Y, Krishna Veni J, Jayasagar G. (2001). Formulation and evaluation of diclofenac sodium using hydrophilic matrices. Drug Dev Ind Pharm, 27:759–766.
   PubMed Web of Science ®Google Scholar
• Melia CD. (1991). Hydrophilic matrix sustained release systems based on polysaccharide carriers. Crit Rev Ther Drug Carrier Syst, 8:395–421.
   PubMed Web of Science ®Google Scholar
• Miranda A, Millán M, Caraballo I. (2006). Study of the critical points of HPMC hydrophilic matrices for controlled drug delivery. Int J Pharm, 311:75–81.
   PubMed Web of Science ®Google Scholar
• Nizar M. Al-Zoubi, Hatim S. AlKhatib, and Wasfy M. Obeidat (2011). Evaluation of hydrophilic matrix tablets based on Carbopol® 971P and low-viscosity sodium alginate for pH-independent controlled drug release. Drug Development and Industrial Pharmacy, 7:789–808.
   Google Scholar
• Nunthanid J, Huanbutta K, Luangtana-Anan M, Sriamornsak P, Limmatvapirat S, Puttipipatkhachorn S. (2008). Development of time-, pH-, and enzyme-controlled colonic drug delivery using spray-dried chitosan acetate and hydroxypropyl methylcellulose. Eur J Pharm Biopharm, 68:253–259.
   PubMed Web of Science ®Google Scholar
• Nykänen P, Krogars K, Säkkinen M, Heinämäki J, Jürjensson H, Veski P et al. (1999). Organic acids as excipients in matrix granules for colon-specific drug delivery. Int J Pharm, 184:251–261.
   PubMed Web of Science ®Google Scholar
• Omidian H, Park K. (2008). Swelling agents and devices in oral drug delivery. J Drug Deliv Sci Tech, 2, 83–93.
   Google Scholar
• Peppas NA, Sahlin J. (1989). A simple equation for the description of solute release. III: Coupling of diffusion and relaxation. Int J Pharm, 57:169–172.
   Web of Science ®Google Scholar
• Perez-Marcos B, Ford JL, Armstrong DJ, Elliott PN, Rostron C, Hogan JE. (1996). Influence of pH on the release of propranolol hydrochloride from matrices containing hydroxypropylmethylcellulose K4M and carbopol 974. J Pharm Sci, 85:330–334.
   PubMed Web of Science ®Google Scholar
• Pygall SR, Kujawinski S, Timmins P, Melia CD. (2009). Mechanisms of drug release in citrate buffered HPMC matrices. Int J Pharm, 370:110–120.
   PubMed Web of Science ®Google Scholar
• Quintanar-Guerrero D, Ganem-Quintanar A, Raygoza-Trejo D, Doelker E. (1999). Relationship between the swelling process and the release of a water-soluble drug from a compressed swellable-soluble matrix of poly(vinyl alcohol). Drug Dev Ind Pharm, 25:169–174.
   PubMed Web of Science ®Google Scholar
• Ritger PL, Peppas NA. (1987). A simple equation for description of solute release II. Fickian and anomalous release from swellable devices. J Control Release, 5:37–42.
   Google Scholar
• Siepmann J, Peppas NA. (2001). Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose (HPMC). Advanced Drug Delivery Reviews, 48:139–157. Siepmann J, Siepmann F. Mathematical modeling of drug delivery. (2008). Int J Pharm, 364:328–343.
   Google Scholar
• Singh B, Rani A, Babita, Ahuja N, Kapil R. (2010). Formulation Optimization of Hydrodynamically Balanced Oral Controlled Release Bioadhesive Tablets of Tramadol Hydrochloride. Sci Pharm, 78:303–323.
   PubMedGoogle Scholar
• Vueba ML, Batista de Carvalho LA, Veiga F, Sousa JJ, Pina ME. (2005). Role of cellulose ether polymers on ibuprofen release from matrix tablets. Drug Dev Ind Pharm, 31:653–665.
   PubMed Web of Science ®Google Scholar
• Lachmann L, Lieberman HA, Kaning J. (2001). teoria e pràtica na industria farmacèutica. Lisboa. vol 2. Fundacào Calouste Gulbenkan. Lisboa, pp 509–597.
   Google Scholar