Piroxicam quantitation in human plasma by high-performance liquid chromatography with on- and off-line solid-phase extraction

Journal of Chromatography. a
M YritiaJ M Barbanoj

Abstract

A comparative study of two analytical methodologies for piroxicam quantitation in plasma by off-line and on-line solid-phase extraction (SPE) and high-performance liquid chromatography (HPLC) is described. The SPE cartridges contained C8 for both extraction methods. The analytes piroxicam and tenoxican (internal standard) were separated on a C18 column with a mobile phase consisting of acetonitrile:20 mM phosphate buffer pH 3.1 (50:50, v/v) followed by UV detection at 360 nm. The validation of the methods demonstrated good recoveries (over 90%), sensitivity (limits of quantification of 0.05 microgram/ml with on-line SPE and 0.1 microgram/ml with off-line SPE, based on a 100 microliters and 200 microliters sample volume, respectively), accuracy and precision (better than 9.5%). Both methodologies have been used for bioequivalence studies.

References

Sep 9, 1988·Journal of Chromatography·F D Boudinot, S S Ibrahim
Jan 10, 1986·Journal of Chromatography·P HeizmannK Zinapold

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Citations

Feb 19, 2002·European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences·María Isabel Pascual-RegueraMaría Soledad Castro Ruiz
Oct 9, 2014·Journal of Analytical Methods in Chemistry·Arın Gül DalDilek Doğrukol-Ak
Jul 31, 2003·Journal of Veterinary Pharmacology and Therapeutics·H L HeebR P Hunter
Feb 28, 2007·Journal of Pharmaceutical and Biomedical Analysis·Abdolkarim Abbaspour, Roya Mirzajani
Feb 24, 2001·Journal of Chromatography. a·J S Frit, M Macka

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