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American Journal of PharmTech Research

Published

Spectrophotometric Method Development and Validation for Atazanavir Sulphate and Ritonavir In Bulk and Tablet Dosage form using Absorption Ratio Method

Published in June 2013 Issue 3 (Vol. 3, Issue 3, 2013)

Spectrophotometric Method Development and Validation for Atazanavir Sulphate and Ritonavir In Bulk and Tablet Dosage form using Absorption Ratio Method - Issue cover

Abstract

A simple, economic, accurate Absorption ratio method was developed for the simultaneous estimation of Atazanavir Sulphate and Ritonavir in bulk and tablet dosage form. 0.1M Hydrochloric acid was used as a diluent. 1% Sodium Lauryl Sulphate is used as surfactant to enhance solubility of drugs in 0.1M hydrochloric acid. The absorptions were observed at 262.8nm and 297nm which were selected based on overlap spectra of Atazanavir Sulphate and Ritonavir. The linearity range was found to be 10-20 mg/ml. The proposed method was validated. The reports was expressed that the proposed method was found to be simple, precise, accurate and rapid for the simultaneous estimation of Atazanavir Sulphate and Ritonavir in bulk and tablet dosage form using absorption ratio method. 

Authors (6)

Sathis Kumar Dinakaran

Aditya Institute of Pharmaceut...

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Sravani Machana

Aditya Institute of Pharmaceut...

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Harani Avasarala

Aditya Institute of Pharmaceut...

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Asha Navadeep Dasari

Aditya Institute of Pharmaceut...

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Vamsi Krishna Machana

GIET School of Pharmacy, Rajah...

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Satish Kumar Patamsetti

GIET School of Pharmacy, Rajah...

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Article Information

Article ID:
AJPTR33052
Paper ID:
AJPTR-01-002471
Published Date:
2013-06-01

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Downloads:2,255

How to Cite

Kumar, S., & Machana & Avasarala & Navadeep, A. & Krishna, V. & Kumar, S. (2013). Spectrophotometric Method Development and Validation for Atazanavir Sulphate and Ritonavir In Bulk and Tablet Dosage form using Absorption Ratio Method. American Journal of PharmTech Research, 3(3), xx-xx. https://ajptr.scholarjms.com/articles/732

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