alexa Validated Method Development for Estimation of Formoterol Fumarate and Mometasone Furoate in Metered Dose Inhalation Form by High Performance Liquid Chromatography | Abstract
ISSN: 2155-9872

Journal of Analytical & Bioanalytical Techniques
Open Access

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Research Article

Validated Method Development for Estimation of Formoterol Fumarate and Mometasone Furoate in Metered Dose Inhalation Form by High Performance Liquid Chromatography

Katari Srinivasarao1,2*, Vinayk Gorule3, Venkata Reddiah Ch3 and Venkata Krishna A3

1CMJ University, Modrina Mansion, Laitumkhrah, Meghalaya, India

2Manager-AD, IDA, Jeedimetla, Hyderabad, India

3Bombay University, Matunga, Mumbai, India

*Corresponding Author:
Katari Srinivasarao
Manager-AD, 22-110, IDA
Jeedimetla, Hyderabad
Andhra Pradesh, CMJ University
Modrina Mansion, Laitumkhrah
Meghalaya, India
Tel: +91-9666882927
E-mail: [email protected]

Received date: November 09, 2012; Accepted date: November 26, 2012; Published date: December 03, 2012

Citation: Srinivasarao K, Gorule V, Venkata Reddiah Ch, Venkata Krishna A (2012) Validated Method Development for Estimation of Formoterol Fumarate and Mometasone Furoate in Metered Dose Inhalation Form by High Performance Liquid Chromatography. J Anal Bioanal Tech 3:153. doi: 10.4172/2155-9872.1000153

Copyright: © 2012 Srinivasarao K, 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, precise, accurate, and stability-indicating method is developed and validated for analysis of formoterol fumarate and mometasone furoate in metered dose inhalation formulations. Separation was achieved on a reversed-phase C18 column (150 mm×4.6 mm i.d., 5 μm) using a mobile phase consisting of Sodium dihydrogen orthophosphate buffer/acetonitrile (50:50, v/v) at a flow rate of 1.0 mL/min and UV detection at 220 nm. This method is validated according to united States Pharmacopia requirements for new methods, which include accuracy, precision, selectivity, robustness, and linearity and range. This method shows enough selectivity, accuracy, precision, and linearity and range to satisfy Federal Drugs Administration/International Conference on Harmonization regulatory requirements. The current method demonstrates good linearity over the range 0.01-0.20 mg/mL of formoterol fumarate with r2=0.999 and 0.40-6.00 mg/mL of mometasone furoate with r2=0.999. The average recovery of the method is 99.9% of formoterol fumarate with a relative standard deviation of 1.94% and 101.5% of mometasone furoate with a relative standard deviation of 0.81%. The degree of reproducibility of the results obtained as a result of small deliberate variations in the method parameters and by changing analytical operators has proven that the method is robust and rugged.

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