Volume 7 Issue 2
Apr.  2017
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S. Dey, S. Subhasis Patro, N. Suresh Babu, P.N. Murthy, S.K. Panda. Development and validation of a stability-indicating RP–HPLC method for estimation of atazanavir sulfate in bulk[J]. Journal of Pharmaceutical Analysis, 2017, 7(2): 134-140.
Citation: S. Dey, S. Subhasis Patro, N. Suresh Babu, P.N. Murthy, S.K. Panda. Development and validation of a stability-indicating RP–HPLC method for estimation of atazanavir sulfate in bulk[J]. Journal of Pharmaceutical Analysis, 2017, 7(2): 134-140.

Development and validation of a stability-indicating RP–HPLC method for estimation of atazanavir sulfate in bulk

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The authors are grateful to the principal of Royal College of Pharmacy and Health Sciences, Berhampur, Orissa, for providing the facilities for working and also to the laboratory assistance

  • Publish Date: Apr. 10, 2017
  • A stability-indicating reverse phase–high performance liquid chromatography (RP–HPLC) method was developed and validated for the determination of atazanavir sulfate in tablet dosage forms using C18 column Phenomenix (250 mm×4.6 mm, 5μm) with a mobile phase consisting of 900 mL of HPLC grade methanol and 100 mL of water of HPLC grade. The pH was adjusted to 3.55 with acetic acid. The mobile phase was sonicated for 10 min and filtered through a 0.45μm membrane filter at a flow rate of 0.5 mL/min. The detection was carried out at 249 nm and retention time of atazanavir sulfate was found to be 8.323 min. Linearity was observed from 10 to 90μg/mL (coefficient of determination R2 was 0.999) with equation, y=23.427x+37.732. Atazanavir sulfate was subjected to stress conditions including acidic, alkaline, oxidation, photolysis and thermal degradation, and the results showed that it was more sensitive towards acidic degradation. The method was validated as per ICH guidelines.
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