Method development and validation of Ceritinib in bulk and pharmaceutical dosage form by UV spectrophotometry

  • Janardhana Reddy VL Research Scholar, Department of Chemistry, Rayalaseema University, Kurnool, 518007, Andhra Pradesh, India
  • Raveendra Reddy P Department of Chemistry, S. K. University, Anantapur, 513003, Andhra Pradesh, India
  • Sreenivasulu S Department of Chemistry, Rajeev Gandhi Memorial College of Engineering and Technology, Nandhyala, Kurnool, 518502, Andhra Pradesh, India

Abstract

UV spectrophotometric study is the most economical method for studying and validating the drug. In this present study, a new method has been developed and validated for Ceritinib in its bulk form and its dosage form. Ceritinib showed the maximum absorbance at 206nm. The method obeyed Beer Lambert's law and the linearity concentration range was found to be 2-10 μg/ml. The results for other validation parameters were analyzed statistically and were found to fall within the acceptance criteria. The recovery studies and assay studies were found to be satisfactory.

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Published
2018-10-31
How to Cite
VL, Janardhana Reddy; P, Raveendra Reddy; S, Sreenivasulu. Method development and validation of Ceritinib in bulk and pharmaceutical dosage form by UV spectrophotometry. International Journal of Research in Pharmaceutical Sciences, [S.l.], v. 9, n. 4, p. 1141-1145, oct. 2018. ISSN 0975-7538. Available at: <https://pharmascope.org/index.php/ijrps/article/view/1646>. Date accessed: 12 dec. 2018. doi: https://doi.org/10.26452/ijrps.v9i4.1646.
Section
Original Articles
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