alexa Simultaneous Determination of NSAID and Antimicrobial Preservatives Using Validated RP-HPLC Method: An Application in Pharmaceutical and Clinical Laboratories
ISSN : 2153-2435

Pharmaceutica Analytica Acta
Open Access

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Research Article

Simultaneous Determination of NSAID and Antimicrobial Preservatives Using Validated RP-HPLC Method: An Application in Pharmaceutical and Clinical Laboratories

Najmul Hasan1*, Mathurot Chaiharn2, Shabana Naz Shah3, Hira Khalid4 and Abdul Jabbar5

1Department of Microbiology, Faculty of Science, University of Karachi, Karachi-75270, Pakistan

2Division of Biotechnology, Faculty of Science, Maejo University, Chiang Mai 50290, Thailand

3Department of Pharmaceutical Chemistry, Research Institute of Pharmaceutical Sciences, Faculty of Pharmacy, University of Karachi, Karachi-75270, Pakistan

4Department of Chemistry, Government College University, Lahore Pakistan, 54000

5Provincial TB Control reference laboratory, National TB control Programme Peshawar, Pakistan

*Corresponding Author:
Najmul Hasan
Department of Microbiology
Faculty of Science
University of Karachi
Karachi-75270, Pakistan
Tel: 0092-333-366-9331
E-mail: [email protected]

Received Date: Januray 28, 2013; Accepted Date: August 05, 2013; Published Date: August 22, 2013

Citation: Hasan N, Chaiharn M, Shah SN, Khalid H, Jabbar A (2013) Simultaneous Determination of NSAID and Antimicrobial Preservatives Using Validated RPHPLC Method: An Application in Pharmaceutical and Clinical Laboratories. Pharm Anal Acta 4:263. doi: 10.4172/2153-2435.1000263

Copyright: © 2013 Hasan N, 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 stability indicating, accurate, specific, precise and simple high performance liquid chromatographic method has been developed and validated for the simultaneous determination of Dexibuprofen along with its preservatives i.e. Sodium Benzoate, Methylparaben, and Propylparaben in pharmaceutical dosage forms of oral solution and in serum. Acetonitrile: Acetate Buffer: Acetic Acid (0.1 M) (50:50:0.3 v/v/v) (pH 5.5) was the mobile phase at flow rate 1.0 mL min-1 using a Hibar® μBondapak® C18 column monitored at wavelength of 230 nm. The calibration curve was linear with a correlation coefficient of more than 0.9995 for the drugs. The averages of the absolute and relative recoveries were found to be 100.07%, 99.82%, 99.91% and 99.97% for Dexibuprofen, Sodium Benzoate, Methylparaben and Propylparaben respectively with 5 to 25 ng mL-1 limit of quantification and 1.5 to 7 ng mL-1 limit of detection. The drugs were subjected to stress conditions of hydrolysis (acid, base, oxidation, and thermal degradation). Maximum degradation was observed in base and 35% H2O2 while found almost stable in the other stress conditions. The studies of forced degradation prove the stability indicating power of the method. The developed method was validated in accordance to ICH guidelines. The proposed High-performance liquid chromatographic method was successfully applied to quantify the amount of Dexibuprofen and three most common microbial preservatives in bulk, dosage form and physiological fluid.

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