Preparation, Evaluation and Development Celecoxib Prolonged Release (PR) Tablets by using Cellulose Polyacrylic acid – based polymers

Abstract

Adilakshmi, D. et al. Simultaneous Formulation, Estimation and Evaluation of Allopurinol Sustained Release Tablets using various suitable Excipients. Asian Journal of Pharmaceutical Analysis. 2016; 6(3), 155-166.‏ DOI: 10.5958/2231-5675.2016.00025.9 James, H. P. et al. Smart polymers for the controlled delivery of drugs–a concise overview. Acta Pharmaceutica Sinica B. 2014; 4(2), 120-127. doi: 10.1016/j.apsb.2014.02.005 Salve, P. et al. Development and Evaluation of Sustained Release Dosage Form using Hydrophilic and Hydrophobic Materials. Research Journal of Pharmacy and Technology. 2016; 9(5), 481-489.‏ DOI: 10.5958/0974-360X.2016.00089.5 Ismail, R. et al. Formulation and in vitro evaluation of once-daily methyldopa sustained release matrix tablets. Research Journal of Pharmacy and Technology. 2015; 8(2), 161-166.‏ DOI: 10.5958/0974-360X.2015.00029.3 Madhukar, G. A. et al. Optimization of Various Grades of HPMC for Development of Sustained Release Matrix Tablets of Theophylline. Asian Journal of Pharmacy and Technology. 2017; 7(1), 19-26.‏ DOI: 10.5958/2231-5713.2017.00004.6 Qi, X. et al. Floating tablets for controlled release of ofloxacin via compression coating of hydroxypropyl cellulose combined with effervescent agent. International Journal of Pharmaceutics. 2015; 489(1-2), 210-217. doi: 10.1016/j.ijpharm.2015.05.007 Abdulhameed, K. A. A., & Salih, N. A. Controlled Release of Cefixime using Sodium Carboxymethyl Cellulose Polymer. Research Journal of Pharmacy and Technology. 2019; 12(9), 4073-4079.‏ DOI: 10.5958/0974-360X.2019.00701.7 Perez-Marcos, B. et al. Mechanical and drug-release properties of atenolol-carbomer hydrophilic matrix tablets. Journal of Controlled Release. 1991; 17(3), 267-276. ‏doi: 10.1016/0168-3659(91)90145-4 World health organization (WHO). Musculoskeletal conditions. Available at: https://www.who.int/news-room/fact-sheets/detail/musculoskeletal-conditions (дата обращения – 08.02.2021) Thimmasetty, J. et al. Solubility parameter estimation of celecoxib by current methods. Asian Journal of Research in Chemistry. 2009; 2(2), 188-195.‏ Terse, P., and Mallya, R. Formulation and Evaluation of Celecoxib loaded colon Targeted Microsponges. Asian Journal of Research in Pharmaceutical Science. 2020; 10(2), 73-78.‏ DOI: 10.5958/2231-5659.2020.00014.4 Paulson, S. K. et al. Pharmacokinetics of celecoxib after oral administration in dogs and humans: effect of food and site of absorption. Journal of Pharmacology and Experimental Therapeutics. 2001; 297(2), 638-645. Gong, L. et al. Celecoxib pathways: pharmacokinetics and pharmacodynamics. Pharmacogenetics and Genomics. 2012; 22(4), 310-318.‏ doi: 10.1097/FPC.0b013e32834f94cb USP 41- NF36 (2018) The United States Pharmacopeial Convention, USA. Mathur N. et al. Evaluation of quality control parameters on various brands of paracetamol tablet formulation. World J Pharm Pharmaceut Sci. 2015; 4(7):976–984. Ravi, G. et al. Development and Evaluation of oral controlled release tablets of oxybutynin using various polymers. Research Journal of Pharmacy and Technology. 2020; 13(8), 3854-3860.‏ DOI: 10.5958/0974-360X.2020.00682.4 Saha, R. N. et al. Determination of celecoxib in pharmaceutical formulations using UV spectrophotometry and liquid chromatography. Journal of Pharmaceutical and Biomedical Analysis. 2002; 28(3-4), 741-751.‏ doi: 10.1016/S0731-7085(01)00678-1 Mandale, T. R. et al Development and validation of analytical method for simultaneous estimation of amlodipine besylate and celecoxib in pure and combined dosage form. Research Journal of Pharmacy and Technology. 2020; 13(9), 4280-4284.‏ DOI: 10.5958/0974-360X.2020.00756.8 Hamed, R., and Omran, H. Development of dual–release pellets of the non-steroidal anti–inflammatory drug celecoxib. Journal of Drug Delivery Science and Technology. 2020; 55.‏ doi: 10.1016/j.jddst.2019.101419 Biswas, B. K. et al. In vitro release kinetic study of esomeprazole magnesium from methocel K15M and methocel K100 LVCR matrix tablets. Dhaka University Journal of Pharmaceutical Sciences. 2008; 7(1), 39-45. ‏doi.org/10.3329/dujps.v7i1.1216 Wise DL. Handbook of Pharmaceutical Controlled Release Technology. UK: CRC press, (2000). 902 P. ISBN 9780824703691 Tiwari, S.B. et al. Controlled release formulation of tramadol hydrochloride using hydrophilic and hydrophobic matrix system. AAPS PharmSciTech. 2003; 4, 18–23. doi: 10.1208/pt040331 Sawant, V. A. et al. In-Vitro Release Kinetic Study of Mosapride Citrate Dihydrate from Sustained Release Matrix Tablet Containing Two Different Viscosity Grades of HPMC. Research Journal of Pharmaceutical Dosage Forms and Technology. 2009; 1(3), 207-212.‏ Iwata, M., & Ueda, H. Dissolution properties of glibenclamide in combinations with polyvinylpyrrolidone. Drug Development and Industrial Pharmacy. 1996; 22(11), 1161-1165. doi: 10.3109/03639049609065953 Ejikeme, P.M. Investigation of the physicochemical properties of microcrystalline cellulose from agricultural wastes I: orange mesocarp. Cellulose. 2008; 15, 141–147. doi: 10.1007/s10570-007-9147-7 Saeio, K. et al. Factors influencing drug dissolution characteristic from hydrophilic polymer matrix tablet. Scientia Pharmaceutica. 2007; 75(4), 147-164. doi: 10.3797/scipharm.2007.75.147 Maharjan, S. et al. Formulation and Evaluation of sustained release Sodium Alginate beads of Indomethacin. Asian Journal of Pharmacy and Technology. 2019; 9(3), 165-172.‏ DOI: 10.5958/2231-5713.2019.00028.X Sareen, R. et al. Meloxicam carbopol-based gels: characterization and evaluation. Current Drug Delivery. 2011; 8(4), 407-415.‏ Mostafavi, A. et al. Development of a prolonged-release gastroretentive tablet formulation of ciprofloxacin hydrochloride: Pharmacokinetic characterization in healthy human volunteers. International Journal of Pharmaceutics. 2011; 409(1-2), 128-136. doi: 10.1016/j.ijpharm. 2011.02. 035