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


Methodology

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

How to Cite

1.
Golamaru LR, Rajnarayana K, Jayaveera K. . Int J of Pharmc Res [Internet]. 2016Feb.28 [cited 2020Nov.24];6(2):75-80. Available from: https://ssjournals.net/index.php/ijpr/article/view/3017

Issue

Vol. 6 No. 2 (2016): Feb

Section

Research Articles

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