Rp-hplc method development and validation for simultaneous estimation of paracetamol and mefenamic acid in pharmaceutical suspension

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Abstract

Paracetamol (PCT) and mefenamic acid (MFA), in combination, is recommended widely for the treatment of antipyretic and anti-inflammatory conditions. The present works carry a new simple, rapid, precise, accurate, and sensitized method of high-performance liquid chromatography with UV detection for simultaneous quantification of PCT and MFA. The samples are eluted in isocratic mode using a Phenomenex ODS 3V C18 (4.6mm × 250 mm i.d, with a particle size of 5μm) with the mobile composition of methanol: phosphate buffer pH 7.1 (70:30) delivered at a flow rate of 1ml/min with the detection wavelength of 254 nm. It shows good linearity response in the concentration range of 15-35 μg/mL and 6-14 μg/ml for PCT and MFA with the retention times of 3.0 min and 4.8 min, respectively. The quantities of PCT and MFA in pharmaceutical suspension were found to be 99.01% and 101.02%, respectively. The method was quantitatively evaluated according to intracerebral hemorrhage (ICH) guidelines taking into consideration the required parameters, and the results obtained are within acceptable limits. So, the proposed method can be employed in the routine analysis and evaluation of MFA and PCT in both bulk and suspension dosage form.

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Kopparapu, V. N. K., Kasula, P., Ankinapalli, A. K. R., & Venkateswarlu, M. (2019). Rp-hplc method development and validation for simultaneous estimation of paracetamol and mefenamic acid in pharmaceutical suspension. International Journal of Pharmaceutical Quality Assurance, 10(4), 583–587. https://doi.org/10.25258/IJPQA.10.4.4

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