alexa HPLC Determination of Pitavastatin Calcium in Pharmaceutical Dosage Forms | OMICS International
ISSN : 2153-2435

Pharmaceutica Analytica Acta
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Research Article

HPLC Determination of Pitavastatin Calcium in Pharmaceutical Dosage Forms

Nanjappan Satheesh Kumar1,2*, Narayanan Nisha3, Jayabalan Nirmal4, Narayanan Sonali5, J Bagyalakshmi2

1Department of Pharmaceutical Analysis, NIPER-Hyderabad

2Department of Pharmaceutical Analysis, College of Pharmacy, SRIPMS, Coimbatore-641 044, Tamil Nadu, India

3Department of Pharmaceutical Technology, Jadavpur university, Kolkata-700 032, India

4Department of Ocular Pharmacology and Pharmacy, Dr. R. P. Centre, All India Institute of Medical Sciences, New Delhi-110029, India

5Department of Neurobiochemistry, Neuroscience Centre, All India Institute of Medical Sciences, New Delhi-110029, India

*Corresponding Author:
Dr. N. Satheesh Kumar, M. Pharm.
Department of Pharmaceutical Analysis
National Institute of Pharmaceutical Education and Research Balanagar
Hyderabad-500037, India
E-mail: [email protected]

Received date: December 28, 2010; Accepted date: April 05, 2011; Published date: April 08, 2011

Citation: Kumar NS, Nisha N, Nirmal J, Sonali N, Bagyalakshmi J (2011) HPLC Determination of Pitavastatin Calcium in Pharmaceutical Dosage Forms. Pharm Anal Acta 2:119. doi: 10.4172/2153-2435.1000119

Copyright: © 2011 Kumar NS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

A simple, sensitive, reliable and rapid reversed-phase high-performance liquid chromatographic (RP-HPLC) method has been developed and validated for the determination of pitavastatin calcium using paracetamol as internal standard. The chromatographic system consisted of Shimadzu LC-10ATVP Pump, SPD-M10 AVP with PDA detector. Separation was achieved on the phenomenex C 18 (250 x 4.60), 5 μ particle size column in isocratic mode at room temperature. The sample was introduced through an injector valve with a 20 μl, sample loop. 0.5% Acetic acid: Acetonitrile 35:65 (%, v/v), was used as mobile phase with flow rate of 1 ml/min. UV detection was performed at 245 nm. A calibration graph was plotted which showed a linearity range between 1-5 μg/ml with the correlation coefficient of 0.9986. The LOD was 5 ng/ ml, while the LOQ was 20 ng/ml. Validation studies revealed the method is specific, rapid, reliable, and reproducible. To study the validity of the method, recovery studies and repeatability studies were carried out using the same optimum conditions. The system suitability studies were also calculated which includes column efficiency, resolution, capacity factor and peak asymmetrical factor. Therefore the proposed method is reliable, rapid, precise and selective so may be used for the quantitative analysis of pitavastatin calcium.

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