Development and validation of Ilaprazole in bulk and pharmaceutical dosage form by UV spectroscopic method

Authors

  • Deepika Devu MLR Institute of Pharmacy
  • K. B. Shalini MLR Institute of Pharmacy
  • Vineela Chadalavada MLR Institute of Pharmacy

DOI:

https://doi.org/10.7439/ijapa.v4i4.98

Abstract

A simple UV spectroscopic method was developed and validated for the estimation of Ilaprazole in bulk and pharmaceutical dosage form using Acetonitrile: ethanol (50:50) as solvent. The quantification was achieved at 307nm. Beers law was obeyed in the concentration range of 2-12 ?g/ml. The results of analysis have been validated statistically and recovery studies carried out in the range 80-120% to confirm the accuracy of the proposed method. The relative standard deviation was found to be less than 2.0%. The present result shows that the proposed method can be successfully implemented for estimation of Ilaprazole in bulk and its marketed formulations.

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Published

2014-12-30

Issue

Section

Research Articles

How to Cite

1.
Development and validation of Ilaprazole in bulk and pharmaceutical dosage form by UV spectroscopic method. Int J of Adv in Phar Ana [Internet]. 2014 Dec. 30 [cited 2024 Oct. 18];4(4):130-3. Available from: https://ssjournals.co.in/index.php/ijapa/article/view/1570

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