Development and Evaluation of Novel Fast Disintegrating Acetaminophen Tablets
DOI:
https://doi.org/10.37285/ijpsn.2015.8.1.7Abstract
In this study, attempts were made to design and developed disintegrating drug delivery system, Acetaminophen fast disintegrating tablet (AFDT) by combining super disintegrants and direct compression method. Acetaminophen is widely used as “over the counter” and “common household drug” as analgesic and antipyretic along with poor absorption due to first pass metabolism. So we aimed to use our novel delivery system to achieve rapid absorption in patients like mentally ill, bed ridden and those who do not have easy access to water. The (AFDT) were produced by combining three super disintegrants viz. Croscarmellose, Crospovidone and Sodium starch glycolate in 4% w/w as ratio of (1:1, 1:2, 2:1) using direct compression method. The optimized batch (A3) of tablet were evaluated for post – compression parameters like hardness (4.5 ± 0.75 kg.cm2), friability ((0.76 %), wetting time (42 ± 0.92 sec), water absorption ratio (98.6 %), disintegration time (24.00 ± 0.83 sec.) were found to be acceptable according to standard limits. The in vitro release rate of acetaminophen from (AFDT) was found to be more than that simple formulation in pH (5.8) using USP dissolution test apparatus type-II. These results indicated that, the new (AFDT) formulation system combined advantage of faster release of acetaminophen, which had better effects of rapid oral absorption. Therefore, the AFDT may be used as fast disintegrating delivery system for OTC drug with poor absorption due to first pass metabolism.
Downloads
Metrics
Keywords:
Acetaminophen, Superdisintegrant, Direct Compression, Compression parametersDownloads
Published
How to Cite
Issue
Section
References
Aulton ME (1998). Pharmaceutics: The Science of Dosage form Design, 1st Edn. Churchill Livingstone; London. 247.
Carter SJ (1998). In Copper and Gun’s: Tutorial Pharmacy. 6th Edn. CBS Publishers and Distributors. New Delhi. 225.
Chang RK, Guo X, Burnside BA and Cough RA (2000). Fast Dissolving Tablets. Pharm. Tech. 24: 52-58.
Chaturvedi S, Agrawal VK and Singh S (2012). Impact of Superdisintegrants on the Release of oro – Sispersible Tablets of Losartan Potassium: A Comparative Analysis. Sch. Res. Lib. 4(6): 1768-1776.
Dobetti L (2001). Fast-Melting Tablets: Developments and Technologies. Pharma. Tech (Suppl.): 44-50.
Gissinger A and Stamm A (1980). Comparative Evaluation of the Properties of Some Tablet Disintegrants. Drug. Dev. Ind. Pharm. (6): 511-536.
Gorman EA, Rhodes CT and Rudnic EM (1982). An Evaluation of Croscarmellose as a Tablet Disintegrant in Direct Compression Systems. Drug Dev. Ind. Pharm. (8): 397-410.
Government of India (1996). Ministry of Health and Family Welfare. Indian Pharmacopoeia Vol. I and II. The Controller of Publication, New Delhi; 762-10.
Indhumathi D and Rathnam G (2010). Design and Optimization of Orodissolving Tablets of Antidepressant Drug by Super- disintegrants Addition Method. Int J Pharm. Sci Rev Res. 2(2): 1-9.
Khairnar DA, Chaudhari CS and Shelke PA (2014). Super-disintegrants: An Emerging Paradigm in Oro-Dispersible Tablets. Int. j. Biopharm. 5(2): 119-128.
Khinch MP, Gupta MK, Bhandar A, Agrawal D, Sharma N and Gupta S (2010). Effects of Various Superdisintegrants on Drug Release of Orally Disintegrating Tablets. Int J Pharma Res Dev. 2(5): 1-8.
Kuchekar BS and Arumugam V (2001). Fast Dissolving Tablets. Indian J. Pharm. Edu. 35: 150-152.
Lachman L and Lieber HA (1981). Pharmaceutical Dosage Forms of Tablets. Marcel Dekker. 2: 241-243.
Nagendrakumar D, Raju SA, Shirsand SB and Para MS (2009). Design of Fast Dissloving Granisetron HCL Tablets using Novel Co-Processed Superdisintegrants. J Biosci Tech. 1(1): 8-14.
Panagrahi D, Baghel S and Mishra SB (2005). Mouth Dissolving Tablets: An Overview of Preparation Techniques, Evaluation and Patented Technologies. J Pharm Res. 4(3): 35-38.
Patil C and Das S (2011). Effect of Various Superdisintegrant on Drug Release Profile and Disintegration Time of Lamotrigine Orally Disintegrating Tablets. Afr. J. Pharm. Pharmacol. 5(1): 76-82.
Seager H (1998). Drug Delivery Products and the Zydis Fast Dissolving Dosage Forms. J. Pharm. Pharmacol. 50: 350-382.
Shakar AAM, Razzak SMI, Hossain MM, Arif MH and Reza MS (2012). Effect of Superdisintegrants on Some Physical Attributes and Release Profile of Paracetamol Immediate Release Tablets. Bang. Pharm. J. 15(1): 89-94.
Shrivastava P and Sethi V (2013). A Review Article on Superdisintegrants. Int. J. Drug Res. Tech. 3(4): 76-87.
Swati C, Nisha C, Aniruddha R and Bhanudas S (2010). Superdisintegrants Selection for Tramadol Dispersible Tablets. J Basic App. Pharm. Sci. 131(3): 151-157.
Thorsteinn L and Dagny H (2004). Determination of Aqueous Solubility by Heating and Equilibration - A Technical Note. AAPS Pharm. Sci. Tech. 7(1): 501-502.
United State Pharmacopoeia-30 (2009). NF-27.Vol-2. The United State Pharmacopoeial Convention: Rockville; p. – 1266.
Vamshi Priya VA, Rao CG, Reddy DS and Reddy VP (2009). The Effect of Different Superdisintegrants and their Concentrations on Dissolution of Topiramate Immediate Release Tablets. Int J Pharma Sci Nanotech. 2(2): 531-536.
Wayne R and Dipan D (2006). Selecting Superdisintegrants for Orally Disintegrating Tablet Formulations. Pharm. Tech. 44: 83-87.