Development and in vitro- in vivo evaluation of Nitazoxanide sustained release tablets

Authors

  • Lakshminarayana Reddy Golamaru RA Chem Pharma Ltd, Balanagar, Hyderabad, Telangana 500037
  • K. Rajnarayana RA Chem Pharma Ltd, Balanagar, Hyderabad, Telangana 500037
  • K.N. Jayaveera Department of Chemistry, Vemu Institute of Technology, P. Kothakota, Chittoor (Dist), A.P

DOI:

https://doi.org/10.7439/ijpr.v6i2.3017

Abstract

Objective: The objective of the present investigation was to develop a sustained release (SR) tablet formulation of Nitazoxanide. Methods: Nitazoxanide Tablets were prepared by employing wet granulation methods and hydrophilic polymers used as drug release retardants. The dissolution data also evaluated for the drug release mechanism and kinetics. The optimized formulation was subjected for in vivo studies in rabbits. Results: Based on data obtained from the in vitro drug release studies 5%w/w of Methocel K100M was selected as a release retardant. The drug release followed first order kinetics and fickian diffusion. Conclusion: Present investigation indicates that the developed formulation was able to sustain the drug release.

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References

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Published

2016-02-28

Issue

Section

Research Articles

How to Cite

1.
Golamaru LR, Rajnarayana K, Jayaveera K. Development and in vitro- in vivo evaluation of Nitazoxanide sustained release tablets. Int J of Pharmc Res [Internet]. 2016 Feb. 28 [cited 2025 Mar. 14];6(2):75-80. Available from: https://ssjournals.co.in/index.php/ijpr/article/view/3017