Celecoxibin Bulk Drug And Its Tablet Formulation Subjected To Forced Degradation Study

Authors

  • Dr.Sushil D.Patil
  • Sanket Pawar

DOI:

https://doi.org/10.53555/sfs.v8i1.1564

Keywords:

Celecoxib, RP-HPLC, Method Development, Method Validation, Stability, Tablet (CELACT-MD)

Abstract

The Celecoxib drug were subjected to forced degradation conditions and the formed degradation products were well separated and resolved from the drug and excipients on SunFire C18 column (250 × 4.6 mm, 5 μ) using blend of Acetonitrile: Water (80: 20 v/v) pH 7.0 in isocratic mode at a flow rate of 1.0mL/min at an ambient temperature of 28 °C with the detection wavelength at 251nm. The retention time of Celecoxib was found 4.32 min. The linearity was performed in the concentration range of 20-100 ppm with correlation factor of 0.999 for Celecoxib. The percentage purity of Celecoxib tablet was found 99.98%.The drug was found to degrade under acid, alkali condition but found stable under photolytic conditions

Author Biographies

  • Dr.Sushil D.Patil

    MET’s Institute of Pharmacy, Department of Pharmaceutical Chemistry, Bhujbal Knowledge City, Nashik S.P.P University, Pune, Maharashtra,Mobile no.8007827080

  • Sanket Pawar

    Savitribai Phule Pune University, Pune, Maharshtra state, India

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Published

2021-08-31

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Section

Articles