Formulation and Evaluation of Sustained Release Dosage Forms of Norfloxacin

DOI:

https://doi.org/10.37285/ijpsn.2018.11.6.6

Authors

  • C Suja
  • Sismy C

Abstract

The goal of this study was to formulate and evaluate norfloxacin sustained release tablets. Norfloxacin sustained release tablets were prepared by wet granulation method using two polymers such as HPMC K 100 M (hydrophilic polymer) and guar gum (natural polymer) and with three polymer ratios (0.5, 1.0 and 1.5). The prepared granules were evaluated to preformulation studies such as angle of repose, bulk density, tapped density, bulkiness, compressibility index and Hauser’s ratio. All the parameters shows that the granules having good flow properties. Then the formulated tablets were taken to evaluation studies such as hardness, weight variation, friability, drug content and thickness. All the parameters were within the acceptable limits. IR spectral analysis showed that there was no interaction between the drug and polymers. The in vitro release study was performed in phosphate buffer pH 7.4 at 293 nm. The in vitro release study showed that if the polymer ratio is increased, then the release of the drug is prolonged. HPMC K 100M shows a prolonged release when compared to guar gum.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Keywords:

Norfloxacin, Sustained release tablet, HPMC K100, Guar Gum

Downloads

Published

2018-11-30

How to Cite

1.
Suja C, C S. Formulation and Evaluation of Sustained Release Dosage Forms of Norfloxacin. Scopus Indexed [Internet]. 2018 Nov. 30 [cited 2024 Sep. 16];11(6):4331-7. Available from: https://ijpsnonline.com/index.php/ijpsn/article/view/402

Issue

Section

Research Articles

References

Banker GS and Anderson N (1990). The Theory and Practice of Industrial Pharmacy-Tablet.
Brahmankar DM and Jaiswal SB (1995). Bio pharmaceutics and Pharmacokinetics- A Treatise 1:345-347.
Borguist P, Korner A and Larsson A (2006). A model for the drug release from a polymeric matrix tablets-effect of swelling and dissolution. J Controlled Release 113:216-25.
Emeje M, Olaleye O, Isimi C, Fortunak J, Byrn S, and Kunle O (2010). Oral Sustained Release Tablets of Zidovudine Using Binary Blends of Natural and Synthetic Polymers. Biol Pharm Bull 33(9):1561-1567.
Higuichi 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.
Joshi N C, Ahmad Z, Mishra S.K and Singh R (2010). Formulation and Evaluation of Matrix Tablet of Tramadol Hydrochloride. Indian Journal of Pharmaceutical Education and Research Association of Pharmaceutical Teachers of India 1(3):1-78.
Krishnarajan C. Mahesh Reddy, Sasikanth Kanikanti, Senthil Kumar and M. Purushothaman (2013). Formulation and evaluation of sustained release matrix tablets Of Levofloxacin using natural polymer. Pharmacophore 4(5): 146-157.
Kumar S and Gupta SK (2012). Natural polymers, gums and mucilages as excipients in drug delivery. Polim Med 42(3-4):191-197.
Lachman, L, Herbert A. Liberman, and L Joseph Kamig (1991). The Theory and Practice of Industrial Pharmacy.1: 296–302.
Patel Shailendra, Agrawal Shikha and Lodhi Bhekam Singh (2012). Natural binding agents in tablet formulation. International Journal of Pharmaceutical & Biological Archives 3(3): 466-473.
Ratnaparkhi MP and Gupta Jyoti P (2013). Sustained Release Oral Drug Delivery System: An Overview. International Journal of Pharma Research & Review 2(3):11-21.
Saha and Hiremath (2010). Controlled release hydrophilic matrix tablets formulation of isoniazid. AAPS Pharmscitech 9(4): 117-180
Sanjay Bajaj, Dinesh Singla and Neha Sakhuja (2012). Stability testing of pharmaceutical products. JAPS 2(3):129-138.
Santanu Ghosh and BB Barik (2009). Preparation and evaluation of aceclofenac sustained release formulation and comparison of formulated and marketed product. International Journal of Medicine and Medical Sciences 1(9): 375-382.
Shahu PA, Potnis VV, Dangre PV, and Thote LT (2013). Development and validation of simultaneous spectrophotometric estimation of ciprofloxacin hydrochloride and dexamethasone in bulk drug and its formulation. Indo Am J Pharm Res 3:7103–7113.
Veiga F, Saisa T and Pina ME (1997). Influence of Technological Variables on the Release of Theophylline from Hydrophilic Matrix Tablets Drug Develop. Ind. Pharm 23: 547-551.
Yadav Amit S, Kumar P, Ashok R Vinod, B Rao Someshwara, and Kulkarni V Suresh (2010). Design and evaluation of Guar gum based controlled release matrix tablets of zidovudine. Journal of Pharmaceutical Science and Technology 3(1): 156-162.
Yie W. Chein (1991). Novel Drug Delivery System 2(50):1-50.