Determination of Metformin in Human Plasma and Urine by High-Performance Liquid Chromatography Using Small Sample Volume and Conventional Octadecyl Silane Column

Dion Brocks1, Raniah Q. Gabr, Raj S. Padwal

1University of Alberta, Edmonton, AB Canada

Abstract


Purpose: To develop a selective and sensitive high-performance liquid chromatographic method for the determination of metformin in human plasma and urine, using a conventional reverse phase column and low specimen volume. Methods: Extraction of metformin and ranitidine (as internal standard) from plasma and urine samples (100 µL) was performed with a 1-butanol-hexane (50:50, v/v) mixture under alkaline conditions followed by back-extraction into diluted acetic acid. Chromatography was carried out using a C18 column (250 mm×4.6 mm, 5 μm). A mobile phase consisting of acetonitrile and KH2PO4 (34:66, v/v) and sodium dodecyl sulphate (3 mM) was pumped at an isocratic flow rate of 0.7 mL/min. Results: The calibration curves were linear (>0.995) in the concentration ranges of 10–5000 and 2–2000 μg/mL for metformin in plasma and urine respectively. The mean absolute recoveries for 100 and 1000 ng/mL metformin in plasma using the present extraction procedure were 93.7 and 88.5%, respectively. The intra- and inter-day coefficients of variation in plasma and urine were <20% at the lowest, and <15% at other concentrations. The percent error values were less than 2% in plasma while it reached ~9% in urine. Conclusions: The method showed high calibres of sensitivity and selectivity for monitoring therapeutic concentrations of metformin in both plasma and urine based on a 0.1 ml sample size.

J Pharm Pharm Sci, 13 (4): 486-494, 2010

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