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A Novel QbD Based SPE-HPLC Bio-analytical Method for Edaravone in Rat Plasma, A Pharmacokinetic Study

1, 1, 1, 1

  1. 1Quality Assurance Laboratory, Centre of Relevance and Excellence in Novel Drug Delivery System, Pharmacy Department, G. H. Patel Building, Donor’s Plaza, The Maharaja Sayajirao University of Baroda, Fatehgunj, Vadodara, Gujarat, INDIA.

CORRESPONDENCE

Sadhana Rajput,

Quality Assurance Laboratory, Centre of Relevance and Excellence in Novel Drug Delivery System, Pharmacy Department, G. H. Patel Building, Donor’s Plaza, The Maharaja Sayajirao University of Baroda, Fatehgunj, Vadodara, Gujarat, INDIA.

sjrajput@gmail.com

Received: 07-04-2016; Accepted: 11-06-2016.

Volume 50, Issue 4 · pp. 563-573 · 2016 · DOI: 10.5530/ijper.50.4.8

ABSTRACT

A simple, sensitive and feasible Quality by design based RP-HPLC bioanalytical method was developed and validated for Edaravone. Plackett burman design and 3¥3 full factorial designs were utilized for factor screening and optimization respectively, to achieve well resolved asymmetric peaks of both internal standard and drug with good theoretical plates. The optimized chromatographic peak was obtained with mobile phase composition of 10 mM ammonium acetate buffer (pH 6) and acetonitrile (60:40, v/v) at a flow rate of 1.0 ml/m and detection wavelength of 243 nm using Kromasil C18 (250 mm × 4.6 mm; 5 μm) column. Non normality, skewness or outliers did not exist as demonstrated by residual plot. To eliminate the possible interferences in the biological matrices, a new solid-phase extraction method using STRATA X C18 Phenomenex cartridges was developed and evaluated. The method was validated as per USFDA guideline. The developed method was efficiently applied to pharmacokinetic study in rat plasma.

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    Fanse, S., Baghel, M., Bhamre, P., & Rajput, S. (2016). A Novel QbD Based SPE-HPLC Bio-analytical Method for Edaravone in Rat Plasma, A Pharmacokinetic Study. Indian Journal of Pharmaceutical Education and Research, 50(4), 563-573. https://doi.org/10.5530/ijper.50.4.8

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    © 2016 Author(s)

    This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. CC BY 4.0