Formulation and Invitro Evaluation of Effervescent Floating Tablets of Hydrophilic Polymers Using Propranolol Hydrochloride as a Model Drug
Abstract
Objective: The main aim of this project is to formulate and in vitro evaluation of effervescent drug delivery using Propanolol HCl as a model drug.
Methodology: The effervescent floating drug delivery was prepared using hydrophilic polymer in two different grades, HPMC K4M and HPMC K200M. Sodium carbonate is used as a gas-generating agent in floating tablets. The tablets were prepared by the wet granulation method. The ratio of HPMC to ethyl cellulose was kept constant at 2:1. The formulated tablets were evaluated for physicochemical properties, in vitro buoyancy, floating properties, swelling studies, in vitro dissolution studies, and drug release kinetics.
Results: The result of in vitro dissolution showed that the sustained release can be achieved using HPMC and increasing the concentration of hydrophilic polymers like HPMC K4M and HPMC K200M increases the capacity of holding the drug within the polymer for a longer time. However, changing the viscosity of the HPMC had no significant difference in the drug release profile. The floating lag time for all the formulations was found to be less than 2 minutes with a floating time of more than 24 hours which showed the adequate buoyancy of the tablets.
Conclusion: The present studies showed that using hydrophilic polymers like HPMC K4M and HPMC K200M along with ethyl cellulose and sodium carbonate as gas generating agents can be used for developing sustained released effervescent floating tablets.
Keywords:
Propranolol Hydrochloride, gastro retentive drug delivery system, floating drug delivery, HPMCDOI
https://doi.org/10.37022/wjcmpr.v7i1.354References
Pant S, Badola A, Kothiyal P. A review on gastroretentive drug delivery system. Indian J Pharm Biol Res. 2016 Jun 30;4(2):01–10.
Khan MA, T Shafeeq. Role of Mathematical Modeling in Controlled Drug Delivery. J Sci Res. 2009 Aug 29;1(3):539–50.
RJPT - [Internet]. [cited 2024 Nov 11]. Available from: https://rjptonline.org/HTMLPaper.aspx?Journal=Research+Journal+of+Pharmacy+and+Technology%3bPID%3d2008-1-4-63
Dixit N. Floating drug delivery system. J Curr Pharm Res. 2011;7(1):6–20.
Chhetri HP, Thapa P. An Overview on Gastroretentive Drug Delivery System. Kathmandu Univ J Sci Eng Technol. 2014 Nov 30;10(1):90–103.
Kumar MR, Satyanarayana B, Paladugu ND, Muddasar S, Pasha SI, Vemireddy S, et al. A Comprehensive Review on Gastro Retentive Drug Delivery System, Acta Chimica & Pharmaceutica Indica: 3(2), 2013, 149-164
Chowdary KPR, Chaitanya KL. Recent research on floating drug delivery systems-a review. Journal of Global Trends in Pharmaceutical Sciences.Volume 5, Issue 1, pp -1361-1373, January-March 2014
Jagdale SC, Agavekar AJ, Pandya SV, Kuchekar BS, Chabukswar AR. Formulation and Evaluation of Gastroretentive Drug Delivery System of Propranolol Hydrochloride. AAPS PharmSciTech. 2009 Sep 1;10(3):1071–9.
Meka VS, Dharmanlingam SR, Kolapalli VRM. Formulation of gastroretentive floating drug delivery system using hydrophilic polymers and its in vitro characterization. Braz J Pharm Sci. 2014 Apr;50(2):431–9.
Tripathi K. Antihypertensive drugs, essentials of medical pharmacology. In: Essentials of Medical Phamacology. 5th ed. Newdelhi: Jaypee Brothers; 2003. p. 235–6.
Pharmacopoeialaboratory C, Nagar R. MINISTRY OF HEALTH & FAMILYWELFARE. 1–3.
Ray D, Prusty AK. DESIGNING AND INVITRO STUDIES OF GASTRIC FLOATING TABLETS OF TRAMADOL HYDROCHLORIDE. In 2010 [cited 2024 Nov 11]. Available from: https://www.semanticscholar.org/paper/DESIGNING-AND-IN%C2%ADVITRO-STUDIES-OF-GASTRIC-FLOATING-Ray-Prusty/209418bd15e7050d4f1492377bfd52f1e9099d2f
Meka V, Ram B, Songa S, Rao N, K R V. Gastroretentive drug delivery systems: Novel approaches and its evaluation-A review. Int J Pharm Sci Rev Res. 2011 Oct 5;10:203–16.
Lazarus J, Cooper J. Absorption, Testing, and Clinical Evaluation of Oral Prolonged-Action Drugs. J Pharm Sci. 1961 Sep 1;50(9):715–32.
Higuchi T. Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices. J Pharm Sci. 1963 Dec 1;52(12):1145–9.
Korsmeyer RW, Gurny R, Doelker E, Buri P, Peppas NA. Mechanisms of solute release from porous hydrophilic polymers. Int J Pharm. 1983 May;15(1):25–35.
Gharti KP, Budhathoki U, Thapa P, Bhargava A. Formulation in vitro evaluation of floating tablets of hydroxypropyl methylcellulose and polyethylene oxide using ranitidine hydrochloride as a model drug. J Young Pharm. 2012 Oct;4(4):201–8.
Stamm A, Tritsch JC. Some Considerations on the Liberation of Drugs from Inert Matrices. Drug Dev Ind Pharm. 1986 Jan;12(11–13):2337–53.
Lachman L, A. Lieberman H, L. Kanig J. The Theory and practice of industrial pharmacy. 3rd ed. Bombay: Varghese Pub. House; 1991. 317 p.
Alizadehgiashi M, Shaw JM. Fickian and Non-Fickian Diffusion in Heavy Oil + Light Hydrocarbon Mixtures. Energy Fuels. 2015 Apr 16;29(4):2177–89.
Pandey NK, Ghatuary SK, Dubey A, Jain PK. Formulation and In Vitro Evaluation of Sustained Release Floating Matrix Tablet of Levofloxacin by Direct Compression Method. J Drug Deliv Ther. 2019 Aug 15;9(4-s):398–403.
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