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RP-HPLC Method for Simultaneous Estimation of Paracetamol and Ibuprofen in Tablets


Affiliations
1 Dept. Quality Control and Analytical R and D, Smilax Laboratories Limited, Jeedimetla, Hyderabad-500055, A.P, India
2 Department of Entomology and Plant Pathology, Auburn University, United States
     

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A simple, selective, accurate high Performance Liquid Chromatographic (HPLC) method was developed and validated for the analysis of Paracetamol and Ibuprofen. Chromatographic separation achieved isocratically on a C18 column [Use Inertsil C18, 5 μ, 150 mm×4.6 mm] utilizing a mobile phase of acetonitrile/phosphate buffer (60:40, v/v, pH 7.0) at a flow rate of 0.8 ml/min with UV detection at 260 nm. Aceclofenac was used as an internal standard. The retention time of ibuprofen, paracetamol and aceclofenac was 2.48, 4.45 and 6.34 min respectively. The developed method was validated in terms of accuracy, precision, linearity, limit of detection, limit of quantitation. This study aimed at developing and validating an HPLC method, being simple, accurate and selective, and the proposed method can be used for the estimation of these drugs in combined dosage forms.

Keywords

Paracetamol, Ibuprofen, RP-HPLC, Validation.
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  • RP-HPLC Method for Simultaneous Estimation of Paracetamol and Ibuprofen in Tablets

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Authors

Prasanna Reddy Battu
Dept. Quality Control and Analytical R and D, Smilax Laboratories Limited, Jeedimetla, Hyderabad-500055, A.P, India
M. S. Reddy
Department of Entomology and Plant Pathology, Auburn University, United States

Abstract


A simple, selective, accurate high Performance Liquid Chromatographic (HPLC) method was developed and validated for the analysis of Paracetamol and Ibuprofen. Chromatographic separation achieved isocratically on a C18 column [Use Inertsil C18, 5 μ, 150 mm×4.6 mm] utilizing a mobile phase of acetonitrile/phosphate buffer (60:40, v/v, pH 7.0) at a flow rate of 0.8 ml/min with UV detection at 260 nm. Aceclofenac was used as an internal standard. The retention time of ibuprofen, paracetamol and aceclofenac was 2.48, 4.45 and 6.34 min respectively. The developed method was validated in terms of accuracy, precision, linearity, limit of detection, limit of quantitation. This study aimed at developing and validating an HPLC method, being simple, accurate and selective, and the proposed method can be used for the estimation of these drugs in combined dosage forms.

Keywords


Paracetamol, Ibuprofen, RP-HPLC, Validation.