Drug Res (Stuttg) 2014; 64(08): 412-419
DOI: 10.1055/s-0033-1358748
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Simple and Rapid Determination of Zafirlukast in Plasma by Ultra-performance Liquid Chromatography Tandem Mass Spectrometric Method: Application into Pharmacokinetic Study in Rabbits

M. Iqbal
1   Bioavailability Laboratory, College of Pharmacy, King Saud University, Riyadh, KSA
2   Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, KSA
,
E. Ezzeldin
1   Bioavailability Laboratory, College of Pharmacy, King Saud University, Riyadh, KSA
,
K. A. Al-Rashood
2   Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, KSA
,
K. I. Al-khamees
3   Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, KSA
,
R. M. A. Khan
3   Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, KSA
,
M. Raish
4   Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, KSA
,
T. Anwer
5   Department of Pharmacology, College of Pharmacy, Jazan University, Jazan, KSA
› Author Affiliations
Further Information

Publication History

received 28 August 2013

accepted 29 October 2013

Publication Date:
20 November 2013 (online)

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Abstract

Zafirlukast is a selective leukotriene receptor antagonist used for the prophylaxis and chronic treatment of asthma. The aim of the present study was to develop a simple sensitive ultra-performance liquid chromatography tandem mass spectroscopy method for rapid determination of zafirlukast in plasma. After a simple one step protein precipitation by acetonitrile, zafirlukast and montelukast (IS) were separated on Acquity UPLC BEHTM C18 column (50×2.1 mm, i.d. 1.7 µm, Waters, USA) using a mobile phase of acetonitrile:water containing 10 mM acetic acid (80:20, v/v) at a flow rate of 0.3 mL/min. Zafirlukast and IS were eluted at 0.51 and 1.1 min, respectively with a total run time of only 1.5 min. The mass spectrometric determination was carried out using an electrospray interface operated in the negative mode with multiple reactions monitoring mode. The precursor to product ion transitions of m/z 574.11>462.07 and m/z 584.2>472.1 were used to quantify zafirlukast and IS, respectively. The method was linear in the concentration range of 0.17–600 ng/mL with coefficients of determination greater than 0.996 and lower limit of quantitation of 0.17 ng/mL. Intra-day and inter-day accuracies were 88.3–113.9% and the precisions were ≤12.6%. Zafirlukast was found to stable under various storage and sample processing conditions as per guidelines of bio-analytical method validation. The method developed herein is simple and rapid, and was successfully applied for the pharmacokinetic study in rabbits.