DESIGN AND STATISTICAL OPTIMIZATION OF ANTACID ANALGESIC EFFERVESCENT TABLETS BY USING 2^3 FACTORIAL DESIGN

Authors

  • Om Mahadeorao Bagade Department of Pharmaceutics, PES Modern College of Pharmacy (Ladies), Moshi, Pune 412105
  • Priyanka P. Kharat Department of Pharmaceutics, PES Modern College of Pharmacy (Ladies), Moshi, Pune 412105
  • Rohini R. Pujari Department of Pharmaceutics, PES Modern College of Pharmacy (Ladies), Moshi, Pune 412105
  • V. S. Raskar Emcure Pharmaceutical Ltd, Emcure House, T 184, M. I. D. C., Bhosari, Pune 411026
  • Amruta M. Shete Department of Pharmaceutics, PES Modern College of Pharmacy (Ladies), Moshi, Pune 412105
  • Maduhri D. Vanve Department of Pharmaceutics, PES Modern College of Pharmacy (Ladies), Moshi, Pune 412105

Keywords:

Ibuprofen, Hyperacidity, Effervescence, Palatability, Factorial Design

Abstract

Objective: The present research work was undertaken with an aim to formulate a combination dosage form constituting an antacid and analgesic which may be useful in case of hyperacidity associated headache.

Methods: In this formulation, a mixture of magnesium and aluminium hydroxide was used as the antacid. Ibuprofen was used as analgesic drug while, citric acid and tartaric acid along with sodium bicarbonate were used as effervescent mixture. The prepared tablets of all the formulations were evaluated for physical characterization.

Results: The infra red spectra revealed that there was no chemical interaction between the drug and excipients which showed their compatibility. The results of these studies were found to be within the standard Pharmacopoeial limits. The release character was studied using the disintegration and dissolution studies conducted. The results of 23 factorial design revealed that the amounts of crosspovidone, tartaric acid and citric acid used in effervescent formulation significantly affected the dependent variables i. e. Hardness, friability and disintegration time etc. The stability studies of the tablet formulation showed that the tablets remained stable even after exposing to stress condition of temperatures.

Conclusion: It was thus concluded that by adopting a systematic formulation approach, optimized release mechanism can be reached in the shortest time with minimum efforts.

 

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Author Biography

Om Mahadeorao Bagade, Department of Pharmaceutics, PES Modern College of Pharmacy (Ladies), Moshi, Pune 412105

Department of Pharmaceutics

References

Mohrle R, Liberman, Lachman L, Schwartz. Pharmaceutical Dosage Form, Vol. 1, Marcel Decker Inc: New York; 2005. p. 285-92.

Rajalaksmi G, Vamsi CH, Bhalchandra R, Damodharan N. Formulation and Evaluation of diclofenac potassium effervescent tabletsâ€. Int J Pharm Biomed Res 2011;2(4):237-43.

Shirsand SB, Swami PV, Kokum DV, Sarasija S. Formulation design and optimization of fast dissolving effervescent tablets of Clonazepam. Indian J Pharm Sci 2009;71(5):567–72.

Modi FP, Patel PR. Formulation, Optimization and evaluation of fixed dose combination of moisture barrier film coated bilayer tablet of artesunate and amodiaquine hydrochloride. Int J Pharm Tech Res 2011;3(4):2124-34.

Banerjee ND, Shukla SS, Singh SR. Formulation and Evaluation of antacid analgesic tablet. Int J Pharm Sci Res 2013;4(6);2327-35.

Tripathi KD. Essentials of Medical Pharmacology; 5th edition: 181-2, 594-5.

Herbert A Lieberman, Leon Lachman, Joseph B. Schwartz; pharmaceutical dosage forms: Tablet, Vol. – I 2nd edition; 285.

Indian Pharmacopoeia, Government of India Ministry of Health and Family Welfare, Delhi: Controller of Publications 1996;2:35.

Margadele J, Neil O, Patricia E, Heckelman, Cherie VK, Kristin JR. The Merk Index†14th edition. An Encyclopedia of Chemical: Drug and Biologicalâ€; 47.

Srinath KR, Chowdary P, Palanisamy P, Vamsy KA, Aparna S, Syed SA. Formulation and evaluation of effervescent tablets of paracetamol. Int J Pharm Res Dev 2011;3(3):76-104.

Simona B, Tanja R, Using different experimental designs in drug excipient compatibility studies during the preformulation development of a stable solid dosage formulation. Acta Chim Solv 2010;57:895-903.

Hippisley-Cox J, Coupland C. Risk of myocardial infarction in patients taking cyclo-oxygenase-2 inhibitors or conventional non-steroidal anti-inflammatory drugs: population based nested case-control analysis. Br Med J 2005;330(7504):1342-3.

Mona D, Robertson P, Mary K, William T, John GJ. The pharmacokinetic properties of Fentanyl effervescent buccal tablet. Clin Therapeutics 2006;28(5):707-14.

Poudel A, Palaian S, Shankar PR. Irrational fixed dose combinations in Nepal: need for intervention, Kathmandu University. Med J 2008;6(3):399-405.

Larry L, Augsburger, Stephan W. Hoag; Pharmaceutical Dosage Form: Tablets 3rd edition, CRC Press. 2008. p. 465.

Ravikumar, Sachin RP, Patil MB, Mahesh SP, Mahalaxmi R. Design and characterization of aceclofenac mouth dissolving tablets by effervescent formulation approach. Scholars Res Library 2010;2(1):220-36.

Leon L, Herbert L, Joseph L Kanig. In: Theory and Practice of Industrial Pharmacy. 2nd Edn. Varghese Publication; 1985.

Xing T, Lei W. A novel ketoconazole bioadhesive effervescent tablet for vaginal delivery: Design, in vitro and ‘in vivo’ evaluation. Int J Pharm 2008;350:181–87.

Gennaro AR, Remington NA. The Science and Practice of Pharmacy. Mack publishing Co: Eastern Pennsylvania, USA; 1995;1660-7.

Published

01-09-2014

How to Cite

Bagade, O. M., P. P. Kharat, R. R. Pujari, V. S. Raskar, A. M. Shete, and M. D. Vanve. “DESIGN AND STATISTICAL OPTIMIZATION OF ANTACID ANALGESIC EFFERVESCENT TABLETS BY USING 2^3 FACTORIAL DESIGN”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 6, no. 9, Sept. 2014, pp. 453-9, https://journals.innovareacademics.in/index.php/ijpps/article/view/1862.

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